Merge pull request #1075 from broadinstitute/ldg_bamoutDocs
Add info about multiple input samples (as relevant for M2)
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@ -89,11 +89,12 @@ public class AssemblyBasedCallerArgumentCollection extends StandardCallerArgumen
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}
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}
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/**
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/**
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* The assembled haplotypes will be written as BAM to this file if requested. Really for debugging purposes only.
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* The assembled haplotypes and locally realigned reads will be written as BAM to this file if requested. Really
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* Note that the output here does not include uninformative reads so that not every input read is emitted to the bam.
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* for debugging purposes only. Note that the output here does not include uninformative reads so that not every
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* input read is emitted to the bam.
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*
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*
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* Turning on this mode may result in serious performance cost for the HC. It's really only appropriate to
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* Turning on this mode may result in serious performance cost for the caller. It's really only appropriate to
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* use in specific areas where you want to better understand why the HC is making specific calls.
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* use in specific areas where you want to better understand why the caller is making specific calls.
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*
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*
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* The reads are written out containing an "HC" tag (integer) that encodes which haplotype each read best matches
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* The reads are written out containing an "HC" tag (integer) that encodes which haplotype each read best matches
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* according to the haplotype caller's likelihood calculation. The use of this tag is primarily intended
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* according to the haplotype caller's likelihood calculation. The use of this tag is primarily intended
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@ -101,14 +102,18 @@ public class AssemblyBasedCallerArgumentCollection extends StandardCallerArgumen
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* easily see which reads go with these haplotype.
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* easily see which reads go with these haplotype.
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*
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*
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* Note that the haplotypes (called or all, depending on mode) are emitted as single reads covering the entire
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* Note that the haplotypes (called or all, depending on mode) are emitted as single reads covering the entire
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* active region, coming from read HC and a special read group.
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* active region, coming from sample "HC" and a special read group called "ArtificialHaplotype". This will increase the
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* pileup depth compared to what would be expected from the reads only, especially in complex regions.
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*
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*
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* Note also that only reads that are actually informative about the haplotypes are emitted. By informative we mean
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* Note also that only reads that are actually informative about the haplotypes are emitted. By informative we mean
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* that there's a meaningful difference in the likelihood of the read coming from one haplotype compared to
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* that there's a meaningful difference in the likelihood of the read coming from one haplotype compared to
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* its next best haplotype.
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* its next best haplotype.
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*
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*
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* If multiple BAMs are passed as input to the tool (as is common for M2), then they will be combined in the bamout
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* output and tagged with the appropriate sample names.
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*
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* The best way to visualize the output of this mode is with IGV. Tell IGV to color the alignments by tag,
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* The best way to visualize the output of this mode is with IGV. Tell IGV to color the alignments by tag,
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* and give it the HC tag, so you can see which reads support each haplotype. Finally, you can tell IGV
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* and give it the "HC" tag, so you can see which reads support each haplotype. Finally, you can tell IGV
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* to group by sample, which will separate the potential haplotypes from the reads. All of this can be seen in
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* to group by sample, which will separate the potential haplotypes from the reads. All of this can be seen in
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* <a href="https://www.dropbox.com/s/xvy7sbxpf13x5bp/haplotypecaller%20bamout%20for%20docs.png">this screenshot</a>
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* <a href="https://www.dropbox.com/s/xvy7sbxpf13x5bp/haplotypecaller%20bamout%20for%20docs.png">this screenshot</a>
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*
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*
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