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Thread | Thread Starter | Forum | Replies | Last Post |
some help ! BAM to Fastq | elitatoun | Bioinformatics | 12 | 10-26-2015 04:36 AM |
fastq to bam | hugh_hang | Bioinformatics | 10 | 05-22-2015 01:51 AM |
Conver\ | variadevang | Bioinformatics | 1 | 03-21-2014 03:58 AM |
Convert merged BAM back to per lane BAM or FASTQ file | danielsbrewer | Bioinformatics | 6 | 10-03-2013 08:29 AM |
Reverse engineering BAM files: BAM -> FASTQ | gene coder | Bioinformatics | 3 | 01-03-2012 03:42 PM |
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#1 |
Junior Member
Location: sweden Join Date: Apr 2013
Posts: 2
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hi, I try to convert the bam produced by pacbio sequel platform to fastq file. The output file showed the detailed sequence, but the quality values were all "!". both "bamToFastq" and "samtools bam2fq" were used.
@m54061_161228_010008/4194368/0_66 AGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG + !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! |
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#2 |
Senior Member
Location: Germany Join Date: Apr 2012
Posts: 215
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bam to fastq conversion is actually not something particularly difficult...
Could you paste the corresponding sam record to your example What about the original data (before alignment); how does this look? |
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#3 |
Senior Member
Location: San Francisco Join Date: Aug 2012
Posts: 322
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Sequel data does not have a per base QV value for raw reads. If you calculate CCS first then the quality values will be meaningfully populated.
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#4 |
Senior Member
Location: Oxford, Ohio Join Date: Mar 2012
Posts: 253
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May this will help? https://github.com/PacificBiosciences/bam2fastx
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