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        <link>http://femtoscanonline.nanoscopy.ru/wiki/</link>
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        <title>Selected area analysis</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B0%D0%BD%D0%B0%D0%BB%D0%B8%D0%B7_%D0%B2%D1%8B%D0%B4%D0%B5%D0%BB%D0%B5%D0%BD%D0%BD%D1%8B%D1%85_%D0%BE%D0%B1%D0%BB%D0%B0%D1%81%D1%82%D0%B5%D0%B9?rev=1331723996&amp;do=diff</link>
        <description>Selected area analysis

This function from the Mathematics menu is oriented to determination of surface area and volume in selected region of the image.

To start working with this function one should select an area of interest with standard selection tools: selection of rectangular areas, selection of ellipses, or selection of isolines. The latter is often preferable. When the selection is ready call the</description>
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        <dc:date>2012-03-06T18:22:36+03:00</dc:date>
        <title>Object Analysis</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B0%D0%BD%D0%B0%D0%BB%D0%B8%D0%B7_%D0%B7%D0%B5%D1%80%D0%B5%D0%BD?rev=1331043756&amp;do=diff</link>
        <description>Object Analysis

The object analysis function allows you to highlight objects, calculate their spatial characteristics, and analyze them with the help of a histogram.

The function is called up using menu command Mathematics/Object Analysis or using the button on the Tool Bar::</description>
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        <dc:date>2012-05-03T15:53:33+03:00</dc:date>
        <title>Roughness analisys</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B0%D0%BD%D0%B0%D0%BB%D0%B8%D0%B7_%D1%88%D0%B5%D1%80%D0%BE%D1%85%D0%BE%D0%B2%D0%B0%D1%82%D0%BE%D1%81%D1%82%D0%B8?rev=1336046013&amp;do=diff</link>
        <description>Roughness analisys

Function Roughness analysis in menu Mathematics calculates a set of parameters characterizing the surface roughness in the selected area, or the whole image.

If you call up this function, a dialog box, in which several options for further analysis can be configured, will appear.</description>
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        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Arithmetics</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B0%D1%80%D0%B8%D1%84%D0%BC%D0%B5%D1%82%D0%B8%D0%BA%D0%B0?rev=1331723996&amp;do=diff</link>
        <description>Arithmetics

	*  Add
	*  Substract
	*  Advanced operation</description>
    </item>
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        <dc:date>2012-02-14T16:05:47+03:00</dc:date>
        <title>Select area</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B2%D1%8B%D0%B4%D0%B5%D0%BB%D0%B5%D0%BD%D0%B8%D0%B5?rev=1329221147&amp;do=diff</link>
        <description>Select area

Cursor mode Selection is switched on by default. The surface regions may be selected in this mode for further processing.

There are three instruments for selecting an area of interest in the program. They are combined in the top tool of the toolbar at the left of the image. These are</description>
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        <dc:date>2012-05-03T15:16:31+03:00</dc:date>
        <title>Selection of extended objects (Curve selection)</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B2%D1%8B%D0%B4%D0%B5%D0%BB%D0%B5%D0%BD%D0%B8%D0%B5_%D0%BA%D1%80%D0%B8%D0%B2%D1%8B%D1%85?rev=1336043791&amp;do=diff</link>
        <description>Selection of extended objects (Curve selection)

There are two tools that can be used for selection of extended objects. They are called up by pressing the left mouse button on the toolbar  to the left of the image.



Manual selection of the contours of extended objects</description>
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        <dc:date>2012-08-07T14:56:20+03:00</dc:date>
        <title>Lengthy object selection</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B2%D1%8B%D0%B4%D0%B5%D0%BB%D0%B5%D0%BD%D0%B8%D0%B5_%D0%BF%D1%80%D0%BE%D1%82%D1%8F%D0%B6%D0%B5%D0%BD%D0%BD%D1%8B%D1%85_%D0%BE%D0%B1%D1%8A%D0%B5%D0%BA%D1%82%D0%BE%D0%B2?rev=1344336980&amp;do=diff</link>
        <description>Lengthy object selection

Lengthy object selection mode can be turned on by the appropriate toolbar button, located on the left side of the image window. You should press and hold the «Curve» button (a), until the dropdown panel appears, with the «</description>
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        <dc:date>2012-06-21T11:10:28+03:00</dc:date>
        <title>Detect edges</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B2%D1%8B%D0%B4%D0%B5%D0%BB%D0%B8%D1%82%D1%8C_%D0%B3%D0%B0%D1%80%D0%BD%D0%B8%D1%86%D1%8B?rev=1340262628&amp;do=diff</link>
        <description>Detect edges



This function detects edges of objects using Canny algorithm. This algorithm is considered to be the best to detect edges on noisy images. The algorithm consists of:

	*  Noise Reduction;
	*  Gradient Calculation;
	*  Non-Maximum Suppression which chooses only the points of gradient local maximum in the direction of gradient vector to be pixels of the edges;</description>
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        <dc:date>2012-06-21T14:06:43+03:00</dc:date>
        <title>Enumerate features</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B2%D1%8B%D0%B4%D0%B5%D0%BB%D0%B8%D1%82%D1%8C_%D0%BE%D0%B1%D1%8A%D0%B5%D0%BA%D1%82%D1%8B?rev=1340273203&amp;do=diff</link>
        <description>Enumerate features

The menu command Operations -&gt; Enum Features calls up a function of automatic detecting of features.

[Выделение объектов]

The picture illustrates which parts of a relief are considered as features. The following parameters are calculated:

	*  Average level of the surface, it is then taken for a zero level. To calculate the average level histogram of surface points’ heights distribution is plotted. Coordinate of the maximum of distribution (height of the major part of image…</description>
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        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Fitting</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B2%D1%8B%D1%80%D0%B0%D0%B2%D0%BD%D0%B8%D0%B2%D0%B0%D0%BD%D0%B8%D0%B5?rev=1331723996&amp;do=diff</link>
        <description>Fitting

Often images obtained by AFM have the common slope or the common salience. Such distortions can appear for different reasons. As a rule, they are related to the temperature drift and the non-linearity of the piezoceramic manipulator. This macroscopic surface pattern usually prevents definition of the object’s structure.</description>
    </item>
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        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Spline fitting</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B2%D1%8B%D1%80%D0%B0%D0%B2%D0%BD%D0%B8%D0%B2%D0%B0%D0%BD%D0%B8%D0%B5_%D1%81%D0%BF%D0%BB%D0%B0%D0%B9%D0%BD%D0%BE%D0%BC?rev=1331723996&amp;do=diff</link>
        <description>Spline fitting

Often the surface pattern and distortions that may occur because of the non-linearity of the piezoceramic manipulator as a whole distort the image in such a way that the subtraction of the surface of the second order does not make it vivid enough. FemtoScan software can form bilinear cubic splines for surfaces and subtract splines from surfaces. To subtract a spline please select the</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B2%D1%8B%D1%81%D0%BE%D1%82%D0%B0_%D0%BF%D0%BE_%D0%B8%D0%BD%D1%82%D0%B5%D1%80%D1%84%D0%B5%D1%80%D0%B5%D0%BD%D1%86%D0%B8%D0%BE%D0%BD%D0%BD%D0%BE%D0%B9_%D0%BA%D0%B0%D1%80%D1%82%D0%B8%D0%BD%D0%B5?rev=1336048880&amp;do=diff">
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        <dc:date>2012-05-03T16:41:20+03:00</dc:date>
        <title>Determination of the height of objects based on the interference pattern</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B2%D1%8B%D1%81%D0%BE%D1%82%D0%B0_%D0%BF%D0%BE_%D0%B8%D0%BD%D1%82%D0%B5%D1%80%D1%84%D0%B5%D1%80%D0%B5%D0%BD%D1%86%D0%B8%D0%BE%D0%BD%D0%BD%D0%BE%D0%B9_%D0%BA%D0%B0%D1%80%D1%82%D0%B8%D0%BD%D0%B5?rev=1336048880&amp;do=diff</link>
        <description>Determination of the height of objects based on the interference pattern



This feature is designed for measuring the slope of the growth hillock on the surface of the crystal based on the interference pattern recorded with an optical microscope. Select one or more segments, the slope of which you want to measure. To do this, you can use tools</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B3%D0%B8%D1%81%D1%82%D0%BE%D0%B3%D1%80%D0%B0%D0%BC%D0%BC%D0%B0?rev=1340270822&amp;do=diff">
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        <dc:date>2012-06-21T13:27:02+03:00</dc:date>
        <title>Histogram</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B3%D0%B8%D1%81%D1%82%D0%BE%D0%B3%D1%80%D0%B0%D0%BC%D0%BC%D0%B0?rev=1340270822&amp;do=diff</link>
        <description>Histogram

Operations -&gt; Histogram command which can also be executed by clicking the button on the tool bar

,

calls up a window containing height distribution of surface points. Numerical data at the bottom of the window correspond to position of dashed vertical lines. If you don’t see the dashed vertical lines on the histogram they are probably placed at the left and the right border of the graph.</description>
    </item>
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        <dc:format>text/html</dc:format>
        <dc:date>2012-06-21T11:27:29+03:00</dc:date>
        <title>Gradient filter</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B3%D1%80%D0%B0%D0%B4%D0%B8%D0%B5%D0%BD%D1%82?rev=1340263649&amp;do=diff</link>
        <description>Gradient filter

Gradient is a vector showing the direction of steepest ascent of a function. Absolute value of gradient equals growth rate in this direction. Gradient filter is a difference linear filter. Difference filters including gradient filter are often referred to as</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B8%D0%B7%D0%BC%D0%B5%D0%BD%D0%B8%D1%82%D1%8C_%D1%80%D0%B0%D0%B7%D0%BC%D0%B5%D1%80?rev=1340374178&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-22T18:09:38+03:00</dc:date>
        <title>Resample</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B8%D0%B7%D0%BC%D0%B5%D0%BD%D0%B8%D1%82%D1%8C_%D1%80%D0%B0%D0%B7%D0%BC%D0%B5%D1%80?rev=1340374178&amp;do=diff</link>
        <description>Resample

You can change size and resolution of any image using menu command Operation -&gt; Resample. This function changes discreet value for every axis X, Y, Z in inner data representation.

This function calls up a dialog window containing table with values. Every parameter corresponds to two columns</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B8%D0%BD%D0%B2%D0%B5%D1%80%D1%81%D0%B8%D1%8F_%D0%BF%D0%B0%D0%BB%D0%B8%D1%82%D1%80%D1%8B?rev=1336044616&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-05-03T15:30:16+03:00</dc:date>
        <title>Palette inversion</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B8%D0%BD%D0%B2%D0%B5%D1%80%D1%81%D0%B8%D1%8F_%D0%BF%D0%B0%D0%BB%D0%B8%D1%82%D1%80%D1%8B?rev=1336044616&amp;do=diff</link>
        <description>Palette inversion

The human eye has different sensitivity to different ranges of colors. Sometimes in order to maximize the informativity of the image, it is not sufficient to scale the standard color palette of the image. To highlight details of high-positioned objects, it is easier to use inverted palettes in which tall objects appear darker. Inverted palettes are not in the list of standard palettes, but any of the available palettes can be inverted with the help button</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B8%D0%BD%D0%B2%D0%B5%D1%80%D1%82%D0%B8%D1%80%D0%BE%D0%B2%D0%B0%D1%82%D1%8C?rev=1331723996&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Invert image</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B8%D0%BD%D0%B2%D0%B5%D1%80%D1%82%D0%B8%D1%80%D0%BE%D0%B2%D0%B0%D1%82%D1%8C?rev=1331723996&amp;do=diff</link>
        <description>Invert image

The principle of Invert function from Mathematics menu significantly differs from the color palette Inversion, which can be called with a button on the image toolbar to the left of the image. When you select Invert command from Mathematics menu or press the button 

[Invert button]

the image data transform: the entire range of values from minimum to maximum is rewritten and assigned to image points in reverse order.
The point at which there was the maximum value will be minimal af…</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B8%D0%BD%D1%82%D0%B5%D1%80%D0%B5%D1%81%D1%83%D1%8E%D1%89%D0%B0%D1%8F_%D0%BE%D0%B1%D0%BB%D0%B0%D1%81%D1%82%D1%8C?rev=1340701624&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-26T13:07:04+03:00</dc:date>
        <title>Region of interest</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B8%D0%BD%D1%82%D0%B5%D1%80%D0%B5%D1%81%D1%83%D1%8E%D1%89%D0%B0%D1%8F_%D0%BE%D0%B1%D0%BB%D0%B0%D1%81%D1%82%D1%8C?rev=1340701624&amp;do=diff</link>
        <description>Region of interest

In Autoscaling regime the color palette is automaticaly spreaded out to the whole range of height values on the image (the same will happen if you do the double-click on the palette in Fixed scale regime). You can specify a certain part of the image as a base for autoscaling</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B8%D1%81%D0%BF%D1%80%D0%B0%D0%B2%D0%BB%D0%B5%D0%BD%D0%B8%D0%B5_%D0%B8%D1%81%D0%BA%D0%B0%D0%B6%D0%B5%D0%BD%D0%B8%D0%B9?rev=1340261976&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-21T10:59:36+03:00</dc:date>
        <title>Dewarping</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%B8%D1%81%D0%BF%D1%80%D0%B0%D0%B2%D0%BB%D0%B5%D0%BD%D0%B8%D0%B5_%D0%B8%D1%81%D0%BA%D0%B0%D0%B6%D0%B5%D0%BD%D0%B8%D0%B9?rev=1340261976&amp;do=diff</link>
        <description>Dewarping

The Dewarping  function from  Mathematics menu is used for correction of the image in accordance with calibration data. AFM images can be considerably affected by nonlinearity of piezoelectric manipulator of a microscope.  This leads to enlarging of objects at the edges of image.
After the function is called up a window appears where you need to specify the name of a file with hysteresis coefficients. These coefficients can be obtained using, for example, menu command</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BA%D0%BE%D1%80%D1%80%D0%B5%D0%BB%D1%8F%D1%86%D0%B8%D1%8F?rev=1331724069&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:21:09+03:00</dc:date>
        <title>Correlation Analysis of Images</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BA%D0%BE%D1%80%D1%80%D0%B5%D0%BB%D1%8F%D1%86%D0%B8%D1%8F?rev=1331724069&amp;do=diff</link>
        <description>Correlation Analysis of Images

Correlation -- is a statistical relationship between two or more random variables. Several functions of correlation analysis are realised in the FemtoScan Online program:

	*  Searching for Cross-correlation
	*  Self-correlation
	*  Searching for structure element
	*  Image Stitching

To call this functions use Mathematics menu or buttons on the toolbar.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BB%D0%B8%D0%BD%D0%B5%D0%B9%D0%BA%D0%B0?rev=1331723996&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Measure lengths</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BB%D0%B8%D0%BD%D0%B5%D0%B9%D0%BA%D0%B0?rev=1331723996&amp;do=diff</link>
        <description>Measure lengths

An instrument for lengths and distances measurements - the Linear is situated in the image toolbar:



Specify the start point with the left mouse click. Draw a segment which length you want to measure holding down the mouse button and release it to fix the final point. The length of interval will be written near its start point. If you want to copy this information to the clipboard, use commands</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BB%D0%B8%D0%BD%D0%B5%D0%B9%D0%BD%D1%8B%D0%B5_%D1%84%D0%B8%D0%BB%D1%8C%D1%82%D1%80%D1%8B?rev=1340262933&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-21T11:15:33+03:00</dc:date>
        <title>Linear filters</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BB%D0%B8%D0%BD%D0%B5%D0%B9%D0%BD%D1%8B%D0%B5_%D1%84%D0%B8%D0%BB%D1%8C%D1%82%D1%80%D1%8B?rev=1340262933&amp;do=diff</link>
        <description>Linear filters

Linear Filters are filters described by linear operators, i.e. operators which satisfy linearity requirements:

F(x+y) = F(x) + F(y) и F(Const*x) = Const* F(x).

Besides Affine transformations there are three linear filters in the program:

	*  Gradient filter
	*  Laplace filter
	*  Gauss filter</description>
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        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Median filtering with X Template</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BC%D0%B5%D0%B4%D0%B8%D0%B0%D0%BD%D0%B0_%D1%85?rev=1331723996&amp;do=diff</link>
        <description>Median filtering with X Template

Median filtering with X Template function is similar to the function Median filtering, but the template used in this case has a shape of cross with a size of 3×3 and rotated on 45 degrees. The processing point is in the middle of the cross.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BC%D0%B5%D0%B4%D0%B8%D0%B0%D0%BD%D0%BD%D1%8B%D0%B9_%D1%84%D0%B8%D0%BB%D1%8C%D1%82%D1%80?rev=1331723996&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Median Filter</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BC%D0%B5%D0%B4%D0%B8%D0%B0%D0%BD%D0%BD%D1%8B%D0%B9_%D1%84%D0%B8%D0%BB%D1%8C%D1%82%D1%80?rev=1331723996&amp;do=diff</link>
        <description>Median Filter

Median filtering is a non-linear image processing method which allows to remove sharp peaks, but to leave steps untouched as opposed to averaging.

Let's explain this method using the following example. The row profile is given in the illustration below: the coordinates of the point are shown in the horizontal line, while the value of the point is shown in the vertical line. For the point to be filtered we take its value and those of its neighbors located in certain proximity (for…</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BC%D0%B5%D0%B4%D0%B8%D0%B0%D0%BD%D0%BD%D1%8B%D0%B9_%D1%84%D0%B8%D0%BB%D1%8C%D1%82%D1%80_%D0%BA%D1%80%D0%B5%D1%81%D1%82?rev=1331723996&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Median filtering with Cross Template</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BC%D0%B5%D0%B4%D0%B8%D0%B0%D0%BD%D0%BD%D1%8B%D0%B9_%D1%84%D0%B8%D0%BB%D1%8C%D1%82%D1%80_%D0%BA%D1%80%D0%B5%D1%81%D1%82?rev=1331723996&amp;do=diff</link>
        <description>Median filtering with Cross Template

Median filtering with Cross Template function is similar to the Median filtering function, but the template used in this case has a shape of cross with a size of 3×3. The processing point is in the middle of the cross. 

One can call this function from the</description>
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        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>The main menu</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BC%D0%B5%D0%BD%D1%8E?rev=1331723996&amp;do=diff</link>
        <description>Appears when the line section window is active</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BC%D0%B5%D0%BD%D1%8E_%D0%BC%D0%B0%D1%82%D0%B5%D0%BC%D0%B0%D1%82%D0%B8%D0%BA%D0%B0?rev=1341387573&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-07-04T11:39:33+03:00</dc:date>
        <title>Mathematics menu</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BC%D0%B5%D0%BD%D1%8E_%D0%BC%D0%B0%D1%82%D0%B5%D0%BC%D0%B0%D1%82%D0%B8%D0%BA%D0%B0?rev=1341387573&amp;do=diff</link>
        <description>Mathematics menu

	*  Macros...
	*  Calibration
	*  Axes
	*  Set zero level on Z
	*  Crop
	*  Invert
	*  Average
	*  Sharpen
	*  Wiener filter
	*  Median filter
	*  Median filter Х
	*  Median filter cross
	*  Adjust scale
	*  Flip
	*  Rotate
	*  Fitting
	*  Spline fitting
	*  Smooth area
	*  Arithmetics
		*  Add
		*  Substract
		*  Advanced operation

	*  Dilate
	*  Erode
	*  Tip modeling
	*  Roughness analysis
	*  Selected area analysis
	*  Threshold
	*  Height from interferience figure
	*  Fin…</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BC%D0%B5%D0%BD%D1%8E_%D0%BE%D0%BF%D0%B5%D1%80%D0%B0%D1%86%D0%B8%D0%B8?rev=1340265141&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-21T11:52:21+03:00</dc:date>
        <title>Operations menu</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BC%D0%B5%D0%BD%D1%8E_%D0%BE%D0%BF%D0%B5%D1%80%D0%B0%D1%86%D0%B8%D0%B8?rev=1340265141&amp;do=diff</link>
        <description>Operations menu

	*  Duplicate
	*  Build 3D View
	*  Fourier
	*  Histogram
	*  Enum Features
	*  Find Steps
	*  Convert Curve to Section 
	*  Create Calibration Curve  
	*  Resample</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BC%D0%B5%D1%82%D0%BA%D0%B8?rev=1336044144&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-05-03T15:22:24+03:00</dc:date>
        <title>Marks</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BC%D0%B5%D1%82%D0%BA%D0%B8?rev=1336044144&amp;do=diff</link>
        <description>Marks

Labels can be placed on the image using a special tool.



The type of labels is defined in View menu -&gt; Marks style. If you select field Numbering, a sequence number will be displayed next to each label. Labels can be displayed in the form of Arrows or V-like ticks.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BC%D0%BE%D0%B4%D0%B5%D0%BB%D0%B8%D1%80%D0%BE%D0%B2%D0%B0%D0%BD%D0%B8%D0%B5_%D0%B7%D0%BE%D0%BD%D0%B4%D0%B0?rev=1336045638&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-05-03T15:47:18+03:00</dc:date>
        <title>Tip modeling</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BC%D0%BE%D0%B4%D0%B5%D0%BB%D0%B8%D1%80%D0%BE%D0%B2%D0%B0%D0%BD%D0%B8%D0%B5_%D0%B7%D0%BE%D0%BD%D0%B4%D0%B0?rev=1336045638&amp;do=diff</link>
        <description>Tip modeling

This feature allows you to create and engineer various forms of probes (cone, advanced cone, pyramid, whisker) based on some well-known geometrical parameters. Subsequently, the created images of the probes can be used in morphological filters</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BD%D0%B0%D0%B9%D1%82%D0%B8_%D1%81%D1%82%D1%80%D1%83%D0%BA%D1%82%D1%83%D1%80%D0%BD%D1%8B%D0%B9_%D1%8D%D0%BB%D0%B5%D0%BC%D0%B5%D0%BD%D1%82?rev=1334773612&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-04-18T22:26:52+03:00</dc:date>
        <title>Find structure element</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BD%D0%B0%D0%B9%D1%82%D0%B8_%D1%81%D1%82%D1%80%D1%83%D0%BA%D1%82%D1%83%D1%80%D0%BD%D1%8B%D0%B9_%D1%8D%D0%BB%D0%B5%D0%BC%D0%B5%D0%BD%D1%82?rev=1334773612&amp;do=diff</link>
        <description>Find structure element

It is not rare in scanning probe microscopy and especially in scanning tunnel microscopy that scientists work with highly organized organic films or with cristal structures. Objects of this type are suited to microscopy investigation on molecular level, the images may look spectacular and in some cases it is possible to build the model of cristal or film unit cell. The common problem of images of this type is their noisiness.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BD%D0%B0%D0%B9%D1%82%D0%B8_%D1%81%D1%82%D1%83%D0%BF%D0%B5%D0%BD%D1%8C%D0%BA%D0%B8?rev=1340274357&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-21T14:25:57+03:00</dc:date>
        <title>Find Steps</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BD%D0%B0%D0%B9%D1%82%D0%B8_%D1%81%D1%82%D1%83%D0%BF%D0%B5%D0%BD%D1%8C%D0%BA%D0%B8?rev=1340274357&amp;do=diff</link>
        <description>Find Steps

Crystal surfaces can have steps. It is caused by crystal layer-by-layer growth. Each new layer forms a step on the previous one. As the layer grows the step grows as well gradually moving. The menu command Operations -&gt; Find Steps can be used in description of step growth with time. To use this function you need to take an image obtained by microscope working in special mode in which the same line is scanned through time.</description>
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        <dc:format>text/html</dc:format>
        <dc:date>2012-06-25T11:49:36+03:00</dc:date>
        <title>Find center of mass</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BD%D0%B0%D0%B9%D1%82%D0%B8_%D1%86%D0%B5%D0%BD%D1%82%D1%80_%D0%BC%D0%B0%D1%81%D1%81?rev=1340610576&amp;do=diff</link>
        <description>Find center of mass

Function Mathematics -&gt; Find center of mass determines the location of a center of mass on the image field. The result of the measurement is displayed in a new window in the form of coordinates XY, the point of the center of mass is marked on the image with green.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BE%D0%B1%D1%80%D0%B0%D0%B1%D0%BE%D1%82%D0%BA%D0%B0_%D0%B8%D0%B7%D0%BE%D0%B1%D1%80%D0%B0%D0%B6%D0%B5%D0%BD%D0%B8%D0%B9_%D0%BF%D0%BE%D0%B2%D0%B5%D1%80%D1%85%D0%BD%D0%BE%D1%81%D1%82%D0%B8?rev=1331723996&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Surface image processing</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BE%D0%B1%D1%80%D0%B0%D0%B1%D0%BE%D1%82%D0%BA%D0%B0_%D0%B8%D0%B7%D0%BE%D0%B1%D1%80%D0%B0%D0%B6%D0%B5%D0%BD%D0%B8%D0%B9_%D0%BF%D0%BE%D0%B2%D0%B5%D1%80%D1%85%D0%BD%D0%BE%D1%81%D1%82%D0%B8?rev=1331723996&amp;do=diff</link>
        <description>Surface image processing

	*  Image toolbar
	*  Working with the color palette
	*  Functions from Mathematics menu Background alignment, smoothing filters, data conversion, some methods of analysis 
	*  Functions from Operations menu Data analysis 
	*  Functions from Edit menu Editing and working with the Clipboard 
	*  Preparing images for printing and presentation</description>
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        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Crop</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BE%D0%B1%D1%80%D0%B5%D0%B7%D0%B0%D1%82%D1%8C?rev=1331723996&amp;do=diff</link>
        <description>Crop

Select a rectangular area on the image, call Crop function from Mathematics menu or press the button

[Crop button]

The image will be croped on the border of this area.

If the selected area has a complex shape, the image will be croped on the borders of the rectangle circumscribing the selected area.</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BE%D0%BF%D1%82%D0%B8%D0%BC%D0%B8%D0%B7%D0%B8%D1%80%D0%BE%D0%B2%D0%B0%D1%82%D1%8C_%D1%88%D0%BA%D0%B0%D0%BB%D1%83?rev=1331723996&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Adjust scale</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BE%D0%BF%D1%82%D0%B8%D0%BC%D0%B8%D0%B7%D0%B8%D1%80%D0%BE%D0%B2%D0%B0%D1%82%D1%8C_%D1%88%D0%BA%D0%B0%D0%BB%D1%83?rev=1331723996&amp;do=diff</link>
        <description>Adjust scale

For internal data representation the software uses 16-bit integers. Their values range from -32768 to 32767. For recalculation to the values of the real height, tension, angles, etc., the scaling ratio and the value of the zero offset are used. They are stored separately. All mathematical operations, filtering and transformation are performed in the internal integer representation. That is why in some cases loss of accuracy can occur during rounding or overflow, if integer values h…</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%B0%D0%BB%D0%B8%D1%82%D1%80%D0%B0?rev=1341297968&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-07-03T10:46:08+03:00</dc:date>
        <title>Colour Mapping (Working with the Colour Palette)</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%B0%D0%BB%D0%B8%D1%82%D1%80%D0%B0?rev=1341297968&amp;do=diff</link>
        <description>Colour Mapping (Working with the Colour Palette)

Analog information obtained by the probe microscope, is digitized and represented as a two-dimensional matrix of integers. Each number in the matrix (depending on the scanning mode) could be a value of the tunneling current, or a value of the cantilever deflection, or a value of a more complex function. In order to present these numbers in a more readable form, they are mapped as a two-dimensional graphic image.</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%B0%D0%BD%D0%B5%D0%BB%D1%8C_%D0%B8%D0%BD%D1%81%D1%82%D1%80%D1%83%D0%BC%D0%B5%D0%BD%D1%82%D0%BE%D0%B2?rev=1331723996&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Image toolbar</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%B0%D0%BD%D0%B5%D0%BB%D1%8C_%D0%B8%D0%BD%D1%81%D1%82%D1%80%D1%83%D0%BC%D0%B5%D0%BD%D1%82%D0%BE%D0%B2?rev=1331723996&amp;do=diff</link>
        <description>Image toolbar

There is an image toolbar on the left side of every opened image window. It consists of eight buttons to the basic tools for image processing.



This tools are desined to:

1.    Select areas on the image

2.    Build sections

3.     Measure lengths

4.    Measure angles

5.    Select extended objects

6.    Place marks on the image

7.    Create the effect of illumination on the image

8.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%B0%D1%80%D0%B0%D0%BC%D0%B5%D1%82%D1%80%D1%8B_%D1%88%D0%B5%D1%80%D0%BE%D1%85%D0%BE%D0%B2%D0%B0%D1%82%D0%BE%D1%81%D1%82%D0%B8?rev=1336046924&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-05-03T16:08:44+03:00</dc:date>
        <title>Roughness parameters</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%B0%D1%80%D0%B0%D0%BC%D0%B5%D1%82%D1%80%D1%8B_%D1%88%D0%B5%D1%80%D0%BE%D1%85%D0%BE%D0%B2%D0%B0%D1%82%D0%BE%D1%81%D1%82%D0%B8?rev=1336046924&amp;do=diff</link>
        <description>Roughness parameters

Surface roughness is an aggregate description of surface unevenness with a 
relatively small steps, selected by base line or by base plane for example. In FemtoScan Online program it is possible to evaluate surface roughness for the surface image as well as for the selected section. In the first case one need to call this function from the</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%B5%D1%80%D1%81%D0%B8%D1%81%D1%82%D0%B5%D0%BD%D1%82%D0%BD%D0%B0%D1%8F_%D0%B4%D0%BB%D0%B8%D0%BD%D0%B0?rev=1346866262&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-09-05T21:31:02+03:00</dc:date>
        <title>Persistence length calculation</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%B5%D1%80%D1%81%D0%B8%D1%81%D1%82%D0%B5%D0%BD%D1%82%D0%BD%D0%B0%D1%8F_%D0%B4%D0%BB%D0%B8%D0%BD%D0%B0?rev=1346866262&amp;do=diff</link>
        <description>Persistence length calculation

Add curve

For pesistence length calculation, first you need to choose a curve, using the tool Curve selection.

After selecting the curve, press the button «Add curve to list» . 

The dialog with data file name will be shown. You can choose an existing file or enter a new file name - if no such file exist, it will be created.
The coordinates of the curve points will be stored in this file.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%BE%D0%B2%D0%BE%D1%80%D0%BE%D1%82?rev=1331723996&amp;do=diff">
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        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Rotate image</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%BE%D0%B2%D0%BE%D1%80%D0%BE%D1%82?rev=1331723996&amp;do=diff</link>
        <description>Rotate image

To rotate image use command Rotate from the Mathematics menu or the button



A dialog box will appear, one can select from three types of rotation in it:

	*  Clockwise by 90 degrees;
	*  Counter-clockwise by 90 degrees;
	*  Rotate by an arbitrary angle specified by the user.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%BE%D0%B4%D1%81%D0%B2%D0%B5%D1%82%D0%BA%D0%B0?rev=1336044455&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-05-03T15:27:35+03:00</dc:date>
        <title>Highlighting</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%BE%D0%B4%D1%81%D0%B2%D0%B5%D1%82%D0%BA%D0%B0?rev=1336044455&amp;do=diff</link>
        <description>Highlighting

Side lighting of the surface pattern is used for visual presentation of data, and highlighting of fine details on the image simultaneously with the macroscopic surface pattern. The effect created by highlighting on the image is similar to the effect of sunlight contrasting the details of the surface pattern in the mountainous terrain.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%BE%D1%80%D0%BE%D0%B3%D0%BE%D0%B2%D0%B0%D1%8F_%D1%84%D0%B8%D0%BB%D1%8C%D1%82%D1%80%D0%B0%D1%86%D0%B8%D1%8F?rev=1336048315&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-05-03T16:31:55+03:00</dc:date>
        <title>Threshold filter</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%BE%D1%80%D0%BE%D0%B3%D0%BE%D0%B2%D0%B0%D1%8F_%D1%84%D0%B8%D0%BB%D1%8C%D1%82%D1%80%D0%B0%D1%86%D0%B8%D1%8F?rev=1336048315&amp;do=diff</link>
        <description>Threshold filter

This feature is designed for sorting of points by height. In FemtoScan, filtering based on a single threshold is implemented.

To call up a threshold filter, select it from menu Mathematics or click on the button

.

In this case, a dialog box, where you can set the threshold level (as a fraction of the maximum image height) and determine how the points that appear above and below this level will be processed, will appear.</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%BE%D1%81%D1%82%D0%BE%D1%80%D0%B8%D1%82%D1%8C_3d?rev=1340266187&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-21T12:09:47+03:00</dc:date>
        <title>Build 3D View</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D0%BE%D1%81%D1%82%D0%BE%D1%80%D0%B8%D1%82%D1%8C_3d?rev=1340266187&amp;do=diff</link>
        <description>Build 3D View

Femtoscan allows you to plot three-dimensional images of the surface. To do this call up menu command  Operations -&gt; Build 3D View or click the button on the tool bar:

.

A lot of operations can be done with resulting three-dimensional object:</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D1%80%D0%B5%D0%BE%D0%B1%D1%80%D0%B0%D0%B7%D0%BE%D0%B2%D0%B0%D1%82%D1%8C_%D0%BA%D1%80%D0%B8%D0%B2%D1%83%D1%8E_%D0%B2_%D1%81%D0%B5%D1%87%D0%B5%D0%BD%D0%B8%D0%B5?rev=1340364060&amp;do=diff">
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        <dc:date>2012-06-22T15:21:00+03:00</dc:date>
        <title>Convert curve to section</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D0%BF%D1%80%D0%B5%D0%BE%D0%B1%D1%80%D0%B0%D0%B7%D0%BE%D0%B2%D0%B0%D1%82%D1%8C_%D0%BA%D1%80%D0%B8%D0%B2%D1%83%D1%8E_%D0%B2_%D1%81%D0%B5%D1%87%D0%B5%D0%BD%D0%B8%D0%B5?rev=1340364060&amp;do=diff</link>
        <description>Convert curve to section

It is possible to make a section not only along row, column or segment but also along an arbitrary polyline. In order to do this you must plot the polyline on image using one of the curve selection tools and then run the menu command Operations -&gt; Convert Curve to Section. The section will be displayed in a new window.</description>
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        <dc:format>text/html</dc:format>
        <dc:date>2012-05-03T15:40:24+03:00</dc:date>
        <title>Morphological filters. Erosion</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%8D%D1%80%D0%BE%D0%B7%D0%B8%D1%8F?rev=1336045224&amp;do=diff</link>
        <description>Morphological filters. Erosion

Morphological filters are based on geometric transformation of the shape of one of the objects by means of another. In SPM, these objects are most often the created image and the tip shape model. 

These filters are used to remove widening on surface and object images that appears due to the final shape of the probe, or to remove the effect of ghosting when scanning using whisker-type cantilevers. They are also used for modeling of scanning artifacts.</description>
    </item>
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        <dc:format>text/html</dc:format>
        <dc:date>2012-05-03T15:36:12+03:00</dc:date>
        <title>Morphological filters. Dilation</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%80%D0%B0%D1%81%D1%88%D0%B8%D1%80%D0%B5%D0%BD%D0%B8%D0%B5?rev=1336044972&amp;do=diff</link>
        <description>Morphological filters. Dilation

Morphological filters are based on geometric transformation of the shape of one of the objects by means of another. In SPM, these objects are most often the created image and the tip shape model. 

These filters are used to remove widening on surface and object images that appears due to the final shape of the probe, or to remove the effect of ghosting when scanning using whisker-type cantilevers. They are also used for modeling of scanning artifacts.</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%81%D0%B3%D0%BB%D0%B0%D0%B4%D0%B8%D1%82%D1%8C_%D1%83%D1%87%D0%B0%D1%81%D1%82%D0%BE%D0%BA?rev=1331723996&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Smooth area</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%81%D0%B3%D0%BB%D0%B0%D0%B4%D0%B8%D1%82%D1%8C_%D1%83%D1%87%D0%B0%D1%81%D1%82%D0%BE%D0%BA?rev=1331723996&amp;do=diff</link>
        <description>Smooth area

Surface patch aligning is performed by using the Smooth area command from the Mathematics menu or by clicking on the button



Great data accuracy is needed in order to perform this operation, that is why, firstly, it is necessary to Adjust scale based on the area around the patch of interest or the entire image. Then you need to select the surface patch with unnecessary saliencies. This area will be filled with the aligning surface in accordance with the algorithm selected in the d…</description>
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        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:32:04+03:00</dc:date>
        <title>Build Sections</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%81%D0%B5%D1%87%D0%B5%D0%BD%D0%B8%D1%8F?rev=1331724724&amp;do=diff</link>
        <description>Build Sections

There are three different instruments for sections in the program: Build row cross-section, Column cross-section and arbitrary cross-section. They are grouped into the dropdown panel in the image toolbar:



In order to build row or column cross-section select the point through wich you wish to plot the cross-section. A new window with a line profile will appear and the current position of the line will be shown on the original image. The color and thickness of the line marking t…</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%81%D0%BA%D0%BB%D0%B5%D0%B9%D0%BA%D0%B0_%D0%B8%D0%B7%D0%BE%D0%B1%D1%80%D0%B0%D0%B6%D0%B5%D0%BD%D0%B8%D0%B9?rev=1331724801&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:33:21+03:00</dc:date>
        <title>Image Stitching</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%81%D0%BA%D0%BB%D0%B5%D0%B9%D0%BA%D0%B0_%D0%B8%D0%B7%D0%BE%D0%B1%D1%80%D0%B0%D0%B6%D0%B5%D0%BD%D0%B8%D0%B9?rev=1331724801&amp;do=diff</link>
        <description>Image Stitching

The Image Stitching function is similar to a function of panorama stitching in photo processing. If you have a set of images, made with an overlap of at least 10 %, the function Image stitching enables to combine them into one big image of the surface.</description>
    </item>
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        <dc:format>text/html</dc:format>
        <dc:date>2012-06-22T17:59:42+03:00</dc:date>
        <title>Create calibration curve</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%81%D0%BE%D0%B7%D0%B4%D0%B0%D1%82%D1%8C_%D0%BA%D0%B0%D0%BB%D0%B8%D0%B1%D1%80%D0%BE%D0%B2%D0%BE%D1%87%D0%BD%D1%83%D1%8E_%D0%BA%D1%80%D0%B8%D0%B2%D1%83%D1%8E?rev=1340373582&amp;do=diff</link>
        <description>Create calibration curve

If you have to work with files with evident geometrical distortions caused by microscope scanner you can correct calibration during processing. In order to do this you must have an additional image of calibration lattice or features on the image which can be used for calibration, i.e. features of known size. Calibration file can be created by the following steps:</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%81%D0%BE%D0%B7%D0%B4%D0%B0%D1%82%D1%8C_%D0%BA%D0%BE%D0%BF%D0%B8%D1%8E?rev=1340265602&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-21T12:00:02+03:00</dc:date>
        <title>Duplicate</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%81%D0%BE%D0%B7%D0%B4%D0%B0%D1%82%D1%8C_%D0%BA%D0%BE%D0%BF%D0%B8%D1%8E?rev=1340265602&amp;do=diff</link>
        <description>Duplicate

The Operations -&gt; Duplicate function or the  button allows you to make a copy of any image, curve or section opened in the program.

To make copy of a window select it and then click the  button. If you want to copy a part of the image select this part with standard</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%82%D0%B8%D0%BF%D1%8B_%D0%B4%D0%B0%D0%BD%D0%BD%D1%8B%D1%85?rev=1336292372&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-05-06T12:19:32+03:00</dc:date>
        <title>SPM data formats</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%82%D0%B8%D0%BF%D1%8B_%D0%B4%D0%B0%D0%BD%D0%BD%D1%8B%D1%85?rev=1336292372&amp;do=diff</link>
        <description>SPM data formats

FemtoScan Online is primarily designed to manage the data obtained by Scanning Probe Microscope, but it is also able to work with other SPM data formats

	*  Topography (Height)
	*  Deflection
	*  Phase
	*  Amplitude
	*  Force curve
	*  Force spectroscopy
	*  Force volume</description>
    </item>
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        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Transpose image</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%82%D1%80%D0%B0%D0%BD%D1%81%D0%BF%D0%BE%D0%BD%D0%B8%D1%80%D0%BE%D0%B2%D0%B0%D1%82%D1%8C_%D0%B8%D0%B7%D0%BE%D0%B1%D1%80%D0%B0%D0%B6%D0%B5%D0%BD%D0%B8%D0%B5?rev=1331723996&amp;do=diff</link>
        <description>Transpose image

If you have two images of the same scan area made up in the perpendicular directions (X fast scanning and Y fast scanning), when you may need one of the two operations --  Transpose image (Flip) or Rotate image -- to combine them depending on the microscope manufacturer.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%82%D1%80%D0%B0%D0%BD%D1%81%D0%BF%D0%BE%D1%80%D1%82%D0%B8%D1%80?rev=1336043288&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-05-03T15:08:08+03:00</dc:date>
        <title>Angle measurement</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%82%D1%80%D0%B0%D0%BD%D1%81%D0%BF%D0%BE%D1%80%D1%82%D0%B8%D1%80?rev=1336043288&amp;do=diff</link>
        <description>Angle measurement

The tool for measuring angles between the segments in plane XY - the angle protractor - can be found on the toolbar:



It allows you to measure the angle between two vectors consequently defined on the image using the mouse. First, using the left mouse button, specify the origin of the first segment, and extend the segment up to the end point of the first vector, without releasing the mouse button. Similarly, specify the second vector. On the image, the origins of the vectors…</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%83%D0%B2%D0%B5%D0%BB%D0%B8%D1%87%D0%B8%D1%82%D1%8C_%D1%80%D0%B5%D0%B7%D0%BA%D0%BE%D1%81%D1%82%D1%8C?rev=1331723996&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Sharpening</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%83%D0%B2%D0%B5%D0%BB%D0%B8%D1%87%D0%B8%D1%82%D1%8C_%D1%80%D0%B5%D0%B7%D0%BA%D0%BE%D1%81%D1%82%D1%8C?rev=1331723996&amp;do=diff</link>
        <description>Sharpening

Sharpening is performed by using the Sharpening command from the  Mathematics Menu or by using the button



This operation emphasizes differences between adjacent pixels’ hues and distinguishes barely visible details. During processing of every pixel of the image, the sharpness core – a</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%83%D1%81%D1%80%D0%B5%D0%B4%D0%BD%D0%B5%D0%BD%D0%B8%D0%B5?rev=1331723996&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>Average</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%83%D1%81%D1%80%D0%B5%D0%B4%D0%BD%D0%B5%D0%BD%D0%B8%D0%B5?rev=1331723996&amp;do=diff</link>
        <description>Average

Standard image dithering by averaging is performed by using the Average command from the  Mathematics menu or by clicking on the button



The size of the averaging area is indicated in the opened dialog box. You can select the square matrix of averaging (3х3, 5х5, etc.). Selection of a large averaging area leads to a significant image dithering.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%83%D1%81%D1%80%D0%B5%D0%B4%D0%BD%D0%B5%D0%BD%D0%B8%D0%B5_%D0%BF%D0%BE_%D1%81%D1%82%D1%80%D0%BE%D0%BA%D0%B0%D0%BC?rev=1340261456&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-21T10:50:56+03:00</dc:date>
        <title>Adjusting scan by lines</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%83%D1%81%D1%80%D0%B5%D0%B4%D0%BD%D0%B5%D0%BD%D0%B8%D0%B5_%D0%BF%D0%BE_%D1%81%D1%82%D1%80%D0%BE%D0%BA%D0%B0%D0%BC?rev=1340261456&amp;do=diff</link>
        <description>Adjusting scan by lines

In Scanning Probe Microscopy images are formed line-by-line. There is a preferred direction (direction of line formation) in this case along which the image has characteristic features. The line scanning is fast but a transition from line to line takes some time. It is possible for a disturbance to occur during this transition resulting in shifting of the following lines up or down. The image appears to have a horizontal step absent on the real surface. In order to get r…</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%84%D0%B8%D0%BB%D1%8C%D1%82%D1%80_%D0%B2%D0%B8%D0%BD%D0%B5%D1%80%D0%B0?rev=1341229328&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-07-02T15:42:08+03:00</dc:date>
        <title>Wiener filter</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%84%D0%B8%D0%BB%D1%8C%D1%82%D1%80_%D0%B2%D0%B8%D0%BD%D0%B5%D1%80%D0%B0?rev=1341229328&amp;do=diff</link>
        <description>Wiener filter

This feature is designed to eliminate random noise presented in the image using Wiener filtration method. To call this function use menu command Mathematics -&gt; Wiener filter or click the toolbar button</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%84%D0%B8%D0%BB%D1%8C%D1%82%D1%80_%D0%B3%D0%B0%D1%83%D1%81%D1%81%D0%B0?rev=1340264058&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-21T11:34:18+03:00</dc:date>
        <title>Gauss filter</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%84%D0%B8%D0%BB%D1%8C%D1%82%D1%80_%D0%B3%D0%B0%D1%83%D1%81%D1%81%D0%B0?rev=1340264058&amp;do=diff</link>
        <description>Gauss filter

Gauss filter is a smoothing filter. The simplest of rectangular smoothing filters is  averaging filter.

The smoothing filters are used mostly for noise reduction. Since the noise changes independently from pixel to pixel noises from neighboring pixels compensate each other when summed. The bigger filtration window, the less average intensity of the noise. The side effect of these filters is blurring of image details. The significant flaw of the</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%84%D0%B8%D0%BB%D1%8C%D1%82%D1%80_%D0%BB%D0%B0%D0%BF%D0%BB%D0%B0%D1%81%D0%B0?rev=1340263884&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-21T11:31:24+03:00</dc:date>
        <title>Laplace filter</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%84%D0%B8%D0%BB%D1%8C%D1%82%D1%80_%D0%BB%D0%B0%D0%BF%D0%BB%D0%B0%D1%81%D0%B0?rev=1340263884&amp;do=diff</link>
        <description>Laplace filter

Discrete Laplace operator is an analog of the continuous Laplace operator. It is given by the divergence of the gradient of a function. As well as gradient filter, Laplace filter emphasizes the edges in image.

   

Laplace filter can be called up from menu Mathematics -&gt; Linear filters, The filter uses the following matrix:</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%84%D0%BE%D1%80%D0%BC%D0%B0%D1%82%D1%8B_%D0%B3%D1%80%D0%B0%D1%84%D0%B8%D1%87%D0%B5%D1%81%D0%BA%D0%B8%D1%85_%D0%B4%D0%B0%D0%BD%D0%BD%D1%8B%D1%85?rev=1336377299&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-05-07T11:54:59+03:00</dc:date>
        <title>en:processing:форматы_графических_данных</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%84%D0%BE%D1%80%D0%BC%D0%B0%D1%82%D1%8B_%D0%B3%D1%80%D0%B0%D1%84%D0%B8%D1%87%D0%B5%D1%81%D0%BA%D0%B8%D1%85_%D0%B4%D0%B0%D0%BD%D0%BD%D1%8B%D1%85?rev=1336377299&amp;do=diff</link>
        <description>The FemtoScan Software is able to work with many standard image file formats: Tiff (*.tif), Bitmap (*.bmp) and Jpeg (*.jpg, *.jpeg). The user can access and import the image files by clicking Open from the  File item of the main software menu. If the image file contains the palette information, the palette indices will be converted to the height of the surface. If not, the height of the result surface will correspond to the image intensity.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%84%D0%BE%D1%80%D0%BC%D0%B0%D1%82%D1%8B_%D0%B4%D0%B0%D0%BD%D0%BD%D1%8B%D1%85?rev=1336829602&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-05-12T17:33:22+03:00</dc:date>
        <title>en:processing:форматы_данных</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%84%D0%BE%D1%80%D0%BC%D0%B0%D1%82%D1%8B_%D0%B4%D0%B0%D0%BD%D0%BD%D1%8B%D1%85?rev=1336829602&amp;do=diff</link>
        <description>File Format  File Name Format  Data Type  Surface  Curve  FemtoScan Online  *.spm  +  +  NT-MDT  *.mdt *.sm2  +  +  Nanoeducator  *.spm  +    Aist-NT  *.aist  +  +  Nanoscope II  *. 0??  +    Nanoscope III, IV, V  *. 0??  +  +  Dimension  *. 0??  +  +  Asylum Research (Igor Pro)</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%84%D1%83%D1%80%D1%8C%D0%B5?rev=1340270357&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-21T13:19:17+03:00</dc:date>
        <title>Fourier filtration</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/%D1%84%D1%83%D1%80%D1%8C%D0%B5?rev=1340270357&amp;do=diff</link>
        <description>Fourier filtration

Fourier transform is a powerful tool for processing and analysis of images. The Fourier transform of two-dimensional image can be obtained by command Operations -&gt; Fourier or by clicking the button on the tool bar:

.

Window with Fourier transform will be displayed:</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/3d_%D0%BD%D0%B0%D1%81%D1%82%D1%80%D0%BE%D0%B9%D0%BA%D0%B8?rev=1340268823&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-21T12:53:43+03:00</dc:date>
        <title>3D image preferences window</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/3d_%D0%BD%D0%B0%D1%81%D1%82%D1%80%D0%BE%D0%B9%D0%BA%D0%B8?rev=1340268823&amp;do=diff</link>
        <description>3D image preferences window

There are several tabs in 3D image preferences window:

	*  General
	*  Scale
	*  Decorations
	*  Viewport
	*  Axes
	*  Font
	*  Background
	*  Legend
	*  Text color
	*  Material color
	*  Material Emission
	*  Material Specular
	*  Scene Ambient
	*  Light Ambient
	*  Light Diffuse
	*  Light Specular</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/3d_%D1%83%D1%80%D0%B0%D0%B2%D0%BD%D0%B5%D0%BD%D0%B8%D0%B5_%D0%BE%D1%81%D0%B2%D0%B5%D1%89%D0%B5%D0%BD%D0%BD%D0%BE%D1%81%D1%82%D0%B8?rev=1340268321&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-21T12:45:21+03:00</dc:date>
        <title>en:processing:3d_уравнение_освещенности</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/3d_%D1%83%D1%80%D0%B0%D0%B2%D0%BD%D0%B5%D0%BD%D0%B8%D0%B5_%D0%BE%D1%81%D0%B2%D0%B5%D1%89%D0%B5%D0%BD%D0%BD%D0%BE%D1%81%D1%82%D0%B8?rev=1340268321&amp;do=diff</link>
        <description>Functions from OpenGL library are used to plot 3D view. According to this the parameters used in the 3D regime are similar to the standard OpenGL parameters of lighting equation. The equation is as follows:

, where

	*   - Material Emission,
	*   - Ambient color of the material (Material Color),</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/3d_video?rev=1340269290&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-21T13:01:30+03:00</dc:date>
        <title>Fly-view video recording</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/3d_video?rev=1340269290&amp;do=diff</link>
        <description>Fly-view video recording

Femtoscan allows you to save different scenes of surface view and to record camera shifts between the scenes. It gives a colorful video as a result clearly demonstrating the shape of the surface. Dialog called up by menu command</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/format?rev=1319780845&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2011-10-28T09:47:25+03:00</dc:date>
        <title>File formats</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/format?rev=1319780845&amp;do=diff</link>
        <description>File formats

At the moment the program supports the file formats listed below. 
If you work with the device, which data format is currently not supported, then you can contact the technical support &lt;spm@nanoscopy.net&gt;, send us the sample file and most likely we will add it.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/image_toolbar?rev=1331724801&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:33:21+03:00</dc:date>
        <title>Image toolbar</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/image_toolbar?rev=1331724801&amp;do=diff</link>
        <description>Image toolbar

There is an image toolbar on the left side of every opened image window. It consists of eight buttons to the basic tools for image processing.



This tools are desined to:

1.    Select areas on the image

2.    Build sections

3.     Measure lengths

4.    Measure angles

5.    Select extended objects

6.    Place marks on the image

7.    Create the effect of illumination on the image

8.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/linear?rev=1331724880&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:34:40+03:00</dc:date>
        <title>Measuring the length</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/linear?rev=1331724880&amp;do=diff</link>
        <description>Measuring the length

Instrument for measuring dimensions of objects and distances in the XY plane - Linear - is in the Image toolbar:



Specify the start point with the left mouse click and hold it. Release the button at the place where the measured segment is ended.
The length of the segment will be displayed near the starting point. If you want to save this value to the clipboard, use functions</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/main_window?rev=1344337093&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-08-07T14:58:13+03:00</dc:date>
        <title>Program main window</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/main_window?rev=1344337093&amp;do=diff</link>
        <description>Program main window

For the user's convenience the FemtoScan Software is equipped with built-in graphical user interface (GUI); the figure below illustrates the basic elements and controls of the GUI.

There is a main menu at the top of the main software window. If there are no open images in the program, the menu consists of 6 parts: File, SPM, View, Windows, Online and Help. When the image is opened, the appropriate menu items become available for the user. The toolbars for working with files…</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/menu?rev=1331724943&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:35:43+03:00</dc:date>
        <title>The main menu</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/menu?rev=1331724943&amp;do=diff</link>
        <description>Appears when the line section window is active</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/menu_math?rev=1338282811&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-05-29T13:13:31+03:00</dc:date>
        <title>Mathematics menu</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/menu_math?rev=1338282811&amp;do=diff</link>
        <description>Mathematics menu

	*  Macros...
	*  Crop
	*  Invert
	*  Average
	*  Sharpen
	*  Wiener filter
	*  Median filter
	*  Median filter Х
	*  Median filter cross
	*  Adjust scale
	*  Transpose image
	*  Rotate image
	*  Fitting
	*  Spline fitting
	*  Smooth area
	*  Arifmetics
		*  Add
		*  substract
		*  advanced_operation

	*  Dilate
	*  Erode
	*  Tip modeling
	*  Roughness analysis
	*  Threshold
	*  Height from interferience figure
	*  Find center of mass
	*  Grain analysis
	*  Adjust scan by lines…</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/menu_operations?rev=1331724801&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:33:21+03:00</dc:date>
        <title>Operations menu</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/menu_operations?rev=1331724801&amp;do=diff</link>
        <description>Operations menu

	*  Duplicate
	*  Build 3D view
	*  Fourier
	*  Histogram
	*  Enum features
	*  Find steps
	*  Convert curve to section 
	*  Create calibration curve  
	*  Resample image
	*  Surface area</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/protractor?rev=1331724880&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:34:40+03:00</dc:date>
        <title>Measuring Angles</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/protractor?rev=1331724880&amp;do=diff</link>
        <description>Measuring Angles

Instrument for measuring angles between segments in XY plane - protractor - is in the Image toolbar:



It allows you to measure the angle between two vectors, which were consistently set with the mouse on the image.
Press the left mouse button to specify the beginning of the first segment, holding the mouse button draw a line segment to the end point of the first vector. Similarly, specify the second vector. Beginnings of the vectors will be shown in red, and the ends in green…</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/pulldown_menu?rev=1331724880&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:34:40+03:00</dc:date>
        <title>Dropdown menu</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/pulldown_menu?rev=1331724880&amp;do=diff</link>
        <description>Dropdown menu

Some instruments on the Image toolbar are grouped into the small drop-down panels. These are the tools to select areas on the image surface Selection, to plot the cross sections Sections and to select extended objects Curve selection.



A dropdown tools are marked with the arrows in the right bottom corner of their icon. In order to see the dropdown menu press and hold the left mouse button for a short time. Duration is determined by adjusting the parameter in</description>
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    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/sections?rev=1331724880&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:34:40+03:00</dc:date>
        <title>Build Sections</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/sections?rev=1331724880&amp;do=diff</link>
        <description>Build Sections

There are three different instruments for sections in the program: Build row cross-section, Column cross-section and arbitrary cross-section. They are grouped into the dropdown panel in the image toolbar:



In order to build row or column cross-section select the point through wich you wish to plot the cross-section. A new window with a line profile will appear and the current position of the line will be shown on the original image. The color and thickness of the line marking t…</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/selection?rev=1319783315&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2011-10-28T10:28:35+03:00</dc:date>
        <title>Select area</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/selection?rev=1319783315&amp;do=diff</link>
        <description>Select area

Cursor mode Selection is switched on by default. The surface regions may be selected in this mode for further processing.

There are three instruments for selecting an area of interest in the program. They are combined in the top tool of the toolbar at the left of the image. These are</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/set_z_zerro?rev=1344337068&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-08-07T14:57:48+03:00</dc:date>
        <title>Select zero level on Z</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/set_z_zerro?rev=1344337068&amp;do=diff</link>
        <description>Select zero level on Z

This function can be found in Mathematics menu, it is desined to shift the Z zero level. If you use Selected area analisys function, you can use this operation to calculate objects height and volume more accurately, because objects height in Selected area analisys is calculated from the zero</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/start?rev=1331724180&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:23:00+03:00</dc:date>
        <title>Image processing</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/start?rev=1331724180&amp;do=diff</link>
        <description>Image processing

FemtoScan Online program provides a wide range of image processing and analysis functions. The program is primarily focused on working with the SPM data - three-dimensional surface profile, force curves, arrays of force curves. The better you know the methods described here - the faster and easier you will obtain success in your work with SPM.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/view?rev=1331723996&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-03-14T15:19:56+03:00</dc:date>
        <title>View menu</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/view?rev=1331723996&amp;do=diff</link>
        <description>View menu

Note that this menu looks different when different types of windows are active!

	*  Toolbars
	*  Actual size
	*  Clear
	*  Comment...
	*  Normalize (Standart image size)
	*  Parameters...
	*  Refresh
	*  Region of interest
	*  Resolution...
	*  Show all images
	*  Decorations
	*  Show zoom window
	*  Full screen
	*  Autorefresh
	*  Marks style
	*  Remember palette
	*  Preferences...
	*  Display parameters</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/view_%D0%BE%D1%87%D0%B8%D1%81%D1%82%D0%B8%D1%82%D1%8C?rev=1340699152&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-26T12:25:52+03:00</dc:date>
        <title>Clear curve, marks, decorations</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/view_%D0%BE%D1%87%D0%B8%D1%81%D1%82%D0%B8%D1%82%D1%8C?rev=1340699152&amp;do=diff</link>
        <description>Clear curve, marks, decorations

During the execution of some functions, Object analysis for example , additional decorations may be plotted on the image. In other functions (Enum Features) a large number of marks appears. Finally, you can plot many curves and marks yourself.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/view_%D0%BF%D0%B0%D0%BD%D0%B5%D0%BB%D0%B8?rev=1340621601&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-25T14:53:21+03:00</dc:date>
        <title>Toolbars</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/view_%D0%BF%D0%B0%D0%BD%D0%B5%D0%BB%D0%B8?rev=1340621601&amp;do=diff</link>
        <description>Toolbars

The menu item View -&gt; Toolbars allows you to customize the interface of the main window of the program, the content of the toolbars and Hot key combinations.



Four upper menu items are responsible for displaying of the corresponding elements of the main window:

1. Standart -- Standart toolbar (Open, Save as, Unod, Redo and other functions);</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/view_%D0%BF%D0%B0%D1%80%D0%B0%D0%BC%D0%B5%D1%82%D1%80%D1%8B?rev=1340700235&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-26T12:43:55+03:00</dc:date>
        <title>Parameters</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/view_%D0%BF%D0%B0%D1%80%D0%B0%D0%BC%D0%B5%D1%82%D1%80%D1%8B?rev=1340700235&amp;do=diff</link>
        <description>Parameters

The menu item View -&gt; Parameters is intended to show scanning parameters from the file. The list of parameters may be different depending on the data format.</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/view_%D1%80%D0%B0%D0%B7%D1%80%D0%B5%D1%88%D0%B5%D0%BD%D0%B8%D0%B5?rev=1340708375&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-26T14:59:35+03:00</dc:date>
        <title>Resolution</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/view_%D1%80%D0%B0%D0%B7%D1%80%D0%B5%D1%88%D0%B5%D0%BD%D0%B8%D0%B5?rev=1340708375&amp;do=diff</link>
        <description>Resolution

If by some reason horizontal or vertical scale of the image is misrepresented, you are able to correct it. Use menu command View -&gt; Resolution to do it. It is availiable if a surface image, curve, section, or histogram is active.

If you use</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/view_%D1%80%D0%B5%D0%B0%D0%BB%D1%8C%D0%BD%D1%8B%D0%B9_%D1%80%D0%B0%D0%B7%D0%BC%D0%B5%D1%80?rev=1340696877&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-26T11:47:57+03:00</dc:date>
        <title>Actual pixels</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/view_%D1%80%D0%B5%D0%B0%D0%BB%D1%8C%D0%BD%D1%8B%D0%B9_%D1%80%D0%B0%D0%B7%D0%BC%D0%B5%D1%80?rev=1340696877&amp;do=diff</link>
        <description>Actual pixels

When you run the menu command View -&gt; Actual pixels or press the tool bar button , an activ image will be replotted in its real size, as 512*512 pixels, for example.

If an image is zoomed in or zoomed out, it will be written in the header in percents:</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/view_%D1%81%D1%82%D0%B0%D0%BD%D0%B4%D0%B0%D1%80%D1%82%D0%BD%D1%8B%D0%B9_%D1%80%D0%B0%D0%B7%D0%BC%D0%B5%D1%80?rev=1340700071&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2012-06-26T12:41:11+03:00</dc:date>
        <title>Normalize</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/view_%D1%81%D1%82%D0%B0%D0%BD%D0%B4%D0%B0%D1%80%D1%82%D0%BD%D1%8B%D0%B9_%D1%80%D0%B0%D0%B7%D0%BC%D0%B5%D1%80?rev=1340700071&amp;do=diff</link>
        <description>Normalize

The standart image size in SPM is 512*512 pixels. Undoubtedly some images are bigger while others are smaller. But if you work with a standart screen resolution, it is convinient to work with images of 512*512 pixels. The menu item View -&gt; Normalize</description>
    </item>
    <item rdf:about="http://femtoscanonline.nanoscopy.ru/wiki/en/processing/z_scale?rev=1299065988&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2011-03-02T14:39:48+03:00</dc:date>
        <title>Z scale</title>
        <link>http://femtoscanonline.nanoscopy.ru/wiki/en/processing/z_scale?rev=1299065988&amp;do=diff</link>
        <description>Z scale

There is a color scale and a numerical scale of the data. The numerical values are mapped to the color values. You can choose between several predefined color palettes by right-clicking on the color palette toolbar.

Also there are several mapping modes. The simplest is</description>
    </item>
</rdf:RDF>
