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Thread | Thread Starter | Forum | Replies | Last Post |
How to create a SAM/BAM file from scratch | DNAjunk | Bioinformatics | 9 | 03-23-2012 08:23 AM |
454 .ace to .bam conversion issue | pmiguel | Bioinformatics | 14 | 06-24-2011 12:30 AM |
Failed to View .BAM file in Artemis | rururara | Bioinformatics | 3 | 04-12-2011 09:38 PM |
gsMapper to SAM/BAM | wjeck | 454 Pyrosequencing | 7 | 10-14-2010 06:16 AM |
ACE to SAM/BAM pile-up | JueFish | Bioinformatics | 3 | 06-16-2010 09:39 AM |
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#1 |
Junior Member
Location: USA Join Date: Aug 2012
Posts: 8
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Hi,
I encountered a problem with gsMapper (v2.6) when I tried to align 10M Illumina paired end reads on to 100 large contigs. Even though I set the parameters to output file in ACE and BAM format, neither was generated. Can anybody give me a clue? Also, is there any way to use the gsMapper output files to generate scaffolds based on paired end information? Thanks! |
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#2 |
Senior Member
Location: Adelaide, Australia Join Date: Sep 2010
Posts: 119
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Why are you using gsMapper with Illumina data? Its a GSFLX tool, so I would have thought it would be much easier to use programs designed to work with smaller reads and Illumina tech
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Tags |
ace, bam, gsmapper, scaffold |
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