Difference between revisions of "GotCloud: Variant Calling Pipeline"

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(Created page with 'Back to the beginning [http://genome.sph.umich.edu/wiki/Pipelines] Running umake is straightforward: <code> '''cd ~/myseq''' '''/usr/local/biopipe/bin/umake --conf myconf ???…')
 
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Back to the beginning [http://genome.sph.umich.edu/wiki/Pipelines]
 
Back to the beginning [http://genome.sph.umich.edu/wiki/Pipelines]
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The Variant Calling Pipeline (UMAKE) takes recalibrated BAM files and detects SNPs and calls their genotypes, producing VCF files.
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== Input Data:==
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*Aligned/Processed/Recalibrated BAM files
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*Index file containing Sample IDs & BAM file names
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*Reference files
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*(Optional) Configuration file to override default options
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=== BAM files ===
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=== Index file ===
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=== Reference Files ===
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=== Configuration File ===
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== Running ==
  
 
Running umake is straightforward:
 
Running umake is straightforward:

Revision as of 17:49, 5 November 2012

Back to the beginning [1]

The Variant Calling Pipeline (UMAKE) takes recalibrated BAM files and detects SNPs and calls their genotypes, producing VCF files.

Input Data:

  • Aligned/Processed/Recalibrated BAM files
  • Index file containing Sample IDs & BAM file names
  • Reference files
  • (Optional) Configuration file to override default options

BAM files

Index file

Reference Files

Configuration File

Running

Running umake is straightforward:

cd ~/myseq
/usr/local/biopipe/bin/umake --conf myconf ???
make -f [out-prefix].Makefile -j [# parallel jobs]