Dahlquist:GenePix Pro Software Protocol: Difference between revisions
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== Using GenePix Pro == | == Using GenePix Pro == | ||
[http://www.openwetware.org/images/8/88/GenePix.pdf GenePix Pro 6.0 Software Manual] | |||
* | === Scanner Settings === | ||
* | |||
** | [[Image:Dahlquist_GenePixPro_versioninfo_20150506.jpg]] | ||
* | * Version information for the GenePix Pro software used to scan chips in the Dahlquist Lab. | ||
[[Image:Dahlquist_GenePixPro_HardwareSettings_20150506.jpg]] | |||
* Hardware settings: | |||
** We use a pixel size of 10 microns. | |||
** We use two lines to average. | |||
** We use a focus position of 0. | |||
** We use Auto PMT settings at 100% power (see below). | |||
[[Image:Dahlquist_GenePixPro_AutoPMTSettings_20150506.jpg]] | |||
* Auto PMT settings: | |||
** Saturation tolerance is set to the default value of 0.05%. | |||
[[Image:Dahlquist_GenePixPro_ScanSettings_20150506.jpg]] | |||
* Alignment Options: | |||
** Find irregular features | |||
** Resize features during alignment to minimum diameter 33% and maximum diameter 200% | |||
** Flag features that fail background threshold criteria as Not Found | |||
** Estimate warping and rotation when finding blocks | |||
** Automatic Image Registration: Max translation 10 pixels. | |||
* Saving scanned images: | |||
** Create a folder on the C: drive called "MicroarrayData_yyyymmdd" where yyyymmdd is the current date. | |||
* Save images to this folder as "Single-image TIFF Files (*.tif)". Do '''not''' use TIFF LZW compression (lossless). | |||
** Name files with a Date prefix and Barcode prefix. | |||
=== Gridding and Generating Intensity Data === | === Gridding and Generating Intensity Data === | ||
* Launch GenPix Pro (select Analysis Only) | * Launch GenPix Pro 6.1 (select Analysis Only) | ||
* On the right hand side of the screen, select the File icon | * On the right hand side of the screen, select the File icon | ||
** Select File > Open Images | ** Select File > Open Images | ||
** Navigate to the folder containing your .tif images | ** Navigate to the folder containing your .tif images | ||
** Hold down the Control key while clicking to select both the 532 and 635 wavelength files | ** Hold down the Control key while clicking to select both the 532 and 635 wavelength files | ||
** Click on the Open button | ** Click on the Open button | ||
Line 21: | Line 44: | ||
* On the right hand side of the screen, select the File icon | * On the right hand side of the screen, select the File icon | ||
** Select Load Array List | ** Select Load Array List | ||
** Select the file | ** Select the file [[Media:Ontario_Y6.4Kv7.GAL | Ontario_Y6.4Kv7.GAL]] | ||
*** To download this file, right-click on the link and select "Save link as..." from the context menu that appears. | |||
** Click the Open button | ** Click the Open button | ||
* Using the icon that has an arrow and a square, drag the grids so that they are approximately aligned with the top block of spots | * Using the icon that has an arrow and a square, drag the grids so that they are approximately aligned with the top block of spots | ||
** Click on the icon that looks like a compass, or a circle with cross-hairs, and select Find Array | ** Click on the icon that looks like a compass, or a circle with cross-hairs, and select Find Array, Find All blocks, Align Features | ||
** Click on the icon again, and select Find All Blocks | *** Alternately, you can do this in three steps by: | ||
** Click on the icon again, and select Align Features in All Blocks | **** Click on the icon that looks like a compass, or a circle with cross-hairs, and select Find Array | ||
**** Click on the icon again, and select Find All Blocks | |||
**** Click on the icon again, and select Align Features in All Blocks | |||
* On the right hand side of the screen, select the icon that looks like a table of data (it says B, C, R at the top of it) | * On the right hand side of the screen, select the icon that looks like a table of data (it says B, C, R at the top of it) | ||
* Click on the File icon on the right hand side and select, Save Results As, and save your results as type "GenePix Pro Files (*.gpr)". Save a JPEG image containing all analyzed features. | |||
* Click on the File icon on the right hand side and select, Save Results As, and save your results. | |||
=== Generating an Array Quality Report === | === Generating an Array Quality Report === | ||
* Launch GenePix Pro (select Analysis Only) | * Launch GenePix Pro 6.1 (select Analysis Only) | ||
* On the right hand side of the screen, select the File icon | * On the right hand side of the screen, select the File icon | ||
* File > Open Results | * File > Open Results | ||
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* Select Print | * Select Print | ||
* Save on the Desktop | * Save on the Desktop | ||
* Name the file: | * Name the file: ChipBarcode#_yyyymmdd | ||
* The PDF file will either open on its own or you need to open it from the file you saved it to | * The PDF file will either open on its own or you need to open it from the file you saved it to | ||
<!-- | |||
== Looking at the raw data == | == Looking at the raw data == | ||
Line 71: | Line 95: | ||
* Repeat with ''SWI4'' ([http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=SWI4 ''SWI4'' page at the ''Saccharomyces'' Gene Database]) | * Repeat with ''SWI4'' ([http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=SWI4 ''SWI4'' page at the ''Saccharomyces'' Gene Database]) | ||
* We are expecting that ''NSR1'' should be expressed and that ''SWI4'' should not because it has been deleted from the yeast genome. Is this the case? | * We are expecting that ''NSR1'' should be expressed and that ''SWI4'' should not because it has been deleted from the yeast genome. Is this the case? | ||
--> | |||
== Next Steps == | == Next Steps == | ||
* Go to the [[BIOL478/S13:Microarray Data Analysis | Microarray Data Analysis]] page for the next steps. | * Go to the [[BIOL478/S13:Microarray Data Analysis | Microarray Data Analysis]] page for the next steps. |
Revision as of 11:51, 14 May 2015
Using GenePix Pro
GenePix Pro 6.0 Software Manual
Scanner Settings
- Version information for the GenePix Pro software used to scan chips in the Dahlquist Lab.
- Hardware settings:
- We use a pixel size of 10 microns.
- We use two lines to average.
- We use a focus position of 0.
- We use Auto PMT settings at 100% power (see below).
- Auto PMT settings:
- Saturation tolerance is set to the default value of 0.05%.
- Alignment Options:
- Find irregular features
- Resize features during alignment to minimum diameter 33% and maximum diameter 200%
- Flag features that fail background threshold criteria as Not Found
- Estimate warping and rotation when finding blocks
- Automatic Image Registration: Max translation 10 pixels.
- Saving scanned images:
- Create a folder on the C: drive called "MicroarrayData_yyyymmdd" where yyyymmdd is the current date.
- Save images to this folder as "Single-image TIFF Files (*.tif)". Do not use TIFF LZW compression (lossless).
- Name files with a Date prefix and Barcode prefix.
Gridding and Generating Intensity Data
- Launch GenPix Pro 6.1 (select Analysis Only)
- On the right hand side of the screen, select the File icon
- Select File > Open Images
- Navigate to the folder containing your .tif images
- Hold down the Control key while clicking to select both the 532 and 635 wavelength files
- Click on the Open button
- Use the brightness and contrast sliders on the upper left hand side to adjust your image to see all of the spots
- You can use the magnifying glass icon to zoom in on an area of the image, and the magnifying glass return icon to go back to the whole chip image
- Zoom in so that you can see the entire top block of grids on your screen
- On the right hand side of the screen, select the File icon
- Select Load Array List
- Select the file Ontario_Y6.4Kv7.GAL
- To download this file, right-click on the link and select "Save link as..." from the context menu that appears.
- Click the Open button
- Using the icon that has an arrow and a square, drag the grids so that they are approximately aligned with the top block of spots
- Click on the icon that looks like a compass, or a circle with cross-hairs, and select Find Array, Find All blocks, Align Features
- Alternately, you can do this in three steps by:
- Click on the icon that looks like a compass, or a circle with cross-hairs, and select Find Array
- Click on the icon again, and select Find All Blocks
- Click on the icon again, and select Align Features in All Blocks
- Alternately, you can do this in three steps by:
- Click on the icon that looks like a compass, or a circle with cross-hairs, and select Find Array, Find All blocks, Align Features
- On the right hand side of the screen, select the icon that looks like a table of data (it says B, C, R at the top of it)
- Click on the File icon on the right hand side and select, Save Results As, and save your results as type "GenePix Pro Files (*.gpr)". Save a JPEG image containing all analyzed features.
Generating an Array Quality Report
- Launch GenePix Pro 6.1 (select Analysis Only)
- On the right hand side of the screen, select the File icon
- File > Open Results
- Select the desired file
- Select Report tab at the top of the screen
- On the left side of the screen, under Navigate, select the back arrow or home icon
- Select Array Quality Control
- Adjust Vital Statistic Thresholds values to:
Quality Control Limits Median signal to background > 2.5 Mean of Median background < 500 Median Signal to Noise > 4 Median % >B + 1 StdDev > 90 Feature variation < 0.5 Background Variation < 1.2 Features with Saturated pixels < 3.3% Not Found < 18% Bad Features < 7%
- Select Start
- Select Show Printable Version
- File > Print
- Under Select Printer > Select Adobe PDF
- Select Print
- Save on the Desktop
- Name the file: ChipBarcode#_yyyymmdd
- The PDF file will either open on its own or you need to open it from the file you saved it to
Next Steps
- Go to the Microarray Data Analysis page for the next steps.