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487 bytes added ,  12:26, 30 October 2014
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The <code>bam2FastQ</code> option on the [[bamUtil]] converts a BAM file into FastQ files. This is necessary when only BAM files are delivered but a new alignment is desired. By converting BAM to FastQ files new alignments can be done using FastQ files
 
The <code>bam2FastQ</code> option on the [[bamUtil]] converts a BAM file into FastQ files. This is necessary when only BAM files are delivered but a new alignment is desired. By converting BAM to FastQ files new alignments can be done using FastQ files
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NOTE: This tool does not work on templates that have more than 2 segments.  It does not properly match reads when more than 2 reads have the same read name.
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'''NOTE: This tool does not work on templates that have more than 2 segments.  It does not properly match reads when more than 2 reads have the same read name.'''
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'''NOTE: This tool does not split reads into read group specific FASTQs.  If you want Read Group specific FASTQ files, first run [[BamUtil: splitBam]] to first split the BAM into 1 BAM per Read Group.  Then run bam2FastQ on each bam.'''
    
== How to use it ==
 
== How to use it ==
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Any errors and a summary of how many pairs and unpaired reads were processed are written to stderr.
 
Any errors and a summary of how many pairs and unpaired reads were processed are written to stderr.
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NOTE: This tool does not work on templates that have more than 2 segments.  It does not properly match reads when more than 2 reads have the same read name.
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'''NOTE: This tool does not work on templates that have more than 2 segments.  It does not properly match reads when more than 2 reads have the same read name.'''
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'''NOTE: This tool does not split reads into read group specific FASTQs.  If you want Read Group specific FASTQ files, first run [[BamUtil: splitBam]] to first split the BAM into 1 BAM per Read Group.  Then run bam2FastQ on each bam.'''
    
=== Output Files ===
 
=== Output Files ===

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