Changes between Version 32 and Version 33 of SnpCallingPipeline
- Timestamp:
- Oct 16, 2010 6:33:27 PM (14 years ago)
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SnpCallingPipeline
v32 v33 15 15 16 16 digraph g { 17 size="10,10" 17 size="10,10" 18 node [shape=box,style=filled,color=white] 19 "dbsnp" 20 "reference.fasta" 21 "realign.intervals" 22 "indelcalls.vcf" 23 "chr[1-24].fasta" 24 "flowcell_lane.1fq.gz" 25 "flowcell_lane.2fq.gz" 26 27 node [shape=ellipse,color=yellow] 18 28 19 29 subgraph cluster_0 { 20 30 style=filled; 21 31 color=lightgrey; 22 node [style=filled,color=white];23 32 "reference.fasta" -> RealignerTargetCreator -> "realign.intervals" 24 33 "indelcalls.vcf"-> RealignerTargetCreator … … 45 54 color=lightgrey; 46 55 node [style=filled,color=white]; 47 "flowcell_lane.aligned.bam" -> Merge -> " IndelRealigner"-> FixMateInformation48 "flowcell_lane2.aligned.bam" -> Merge -> "sample.aligned.bam"56 "flowcell_lane.aligned.bam" -> Merge -> "sample.aligned.bam" -> "IndelRealigner"-> FixMateInformation 57 "flowcell_lane2.aligned.bam" -> Merge 49 58 "flowcell_lane3.aligned.bam" -> Merge 50 59 FixMateInformation -> IndelGenotyperV2 -> FilterSingleCalls -> UnifiedGenotyper -> Filtration -> VariantEval -> "QC reports" … … 52 61 label = "Per Sample*Chromosome (750*24=18k)"; 53 62 } 54 55 56 57 58 63 } 59 64