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Type: Improvement
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Status: Closed
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Priority: Minor
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Resolution: Won't Fix
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Affects Version/s: 1.29
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Fix Version/s: None
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Component/s: Basic-MSA, Basic-Nucl
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Labels:
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Story Points:5
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Epic Link:
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Affect Type:Userdefined
Modify the "Contig Assembly with CAP3" dialog as follows:
- Rename the dialog to "De Novo Assemble Sanger Reads with CAP3".
- Rename the first tab inside dialog from "Base" to "General".
- Remove all current widgets from the "General tab and replace them with the following widgets (see also the "Map Sanger Reads to Reference" dialog):
- There should be three groups inside the tab: "Input data", "Main settings", "Result alignment".
- The "Input data" group contains a widget for reads with "Add" and "Remove" buttons. Decrease the vertical size of the reads widget a little bit.
- The "Main settings" group contains three parameters that should be moved there from the "Advanced" tab of the dialog. That is:
- "Base quality cutoff for clipping" (the parameter has the same name on the "Advanced" tab).
- "Min overlap length" (corresponds to "Overlap length cutoff").
- "Min overlap identity" (corresponds to "Overlap percent identity cutoff"). Also, add "%" into the spin box.
- The "Result alignment" group should be as in the "Map Sanger Reads to Reference" dialog: an edit box with the browse button, the "Add to project" checkbox. The default name should be "sanger_reads_alignment.ugenedb" (or "sanger_reads_alignment_1.ugenedb", if the previous file exists, etc.). Note: In some scenarios several output files may be produced by CAP3, in this case the same number auto-incremental rules should be applied to the base file name, specified in this field.
- On the "Advanced" tab:
- Rename the "Clipping for poor regions" to "Clipping of poor regions".
- Remove "Base quality cutoff for clipping (-c)" parameter from the group.
- Add a new parameter "Min number pf good reads at clip position (-z)" to the group (under the "Clipping range (-y)" parameter). The value is an integer number. Min possible value is "1". The default value is "2". Pass "-z VALUE" to the command line launch of the CAP3 external tool.
- Remove the "Length and percent identity of an overlap" group with both parameters.
- Rename "Assembly reverse reads" to "Assemble reverse reads".
- Rename the "Run" button in the dialog to "Assemble".
- blocks
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UGENE-6002 Error on specifying only one input file for CAP3
- Closed
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UGENE-5992 Remember modified values in the CAP3 dialog
- Closed
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UGENE-5995 Edit, map, and assemble items in the Chromatogram View context menu
- Closed
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UGENE-5996 "Sanger data analysis" item in the Project View context menu
- Closed
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UGENE-5997 Drag'n'drop of Sanger reads in the Project View
- Closed
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UGENE-5999 Mode of a Sanger read opening
- Closed
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UGENE-6000 "Read name in result alignment" for Sanger de novo assembly
- Closed
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UGENE-6006 CAP3 output in simple alignment formats
- Closed
- is blocked by
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UGENE-5994 CAP3 output in the UGENE Database format
- Closed
- relates to
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UGENE-5990 Change possible values of CAP3 parameters
- Closed
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UGENE-2330 Selection of CAP3 output file
- Closed