Mercurial > repos > jjohnson > pileup_to_vcf
annotate README @ 9:c0a6e8f595ec default tip
Add option to set VCF ID field value, this can be used to ID germline variants for SnpSift
author | Jim Johnson <jj@umn.edu> |
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date | Thu, 11 Apr 2013 10:28:10 -0500 |
parents | 07cd87e94fbe |
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rev | line source |
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8 | 1 Cconverts the tabular pileup output from samtools mpileup to a VCF file. |
2 Filters on read coverage, base quality and the frequency of a variant. | |
3 The VCF info is populated with a SAF tag that give the specific frequency (0 - 1) of a variant being observed. | |
4 This is used for filtering in the mmuff ( Missense Mutation and Frameshift Finder) workflow. | |
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c0a6e8f595ec
Add option to set VCF ID field value, this can be used to ID germline variants for SnpSift
Jim Johnson <jj@umn.edu>
parents:
8
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changeset
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5 The VCF ID field can be optionally set, which can be used with SnpSift annotate or SnpSift filter. |