Changes between Version 50 and Version 51 of SnpCallingPipeline
- Timestamp:
- Nov 8, 2010 9:05:17 AM (14 years ago)
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SnpCallingPipeline
v50 v51 35 35 style=filled; 36 36 color=lightgrey; 37 37 38 "reference.fasta" -> RealignerTargetCreator -> "realign.intervals" 38 39 "indelcalls.vcf"-> RealignerTargetCreator … … 51 52 "flowcell_lane.2.fq.gz" -> align2 -> alignPE -> MarkDuplicates -> "IndelRealigner & \n FixMateInformation (knownsOnly)" ->"Quality Recalibration"->"flowcell_lane.aligned.bam" 52 53 "realign.intervals" -> "IndelRealigner & \n FixMateInformation (knownsOnly)" 53 label = "Per Lane *Chromosome (750*3*24=54k) ";54 label = "Per Lane (750*3=2250) "; 54 55 } 55 56 … … 69 70 }}} 70 71 72 Discussion 73 74 * How long takes alignment per genome? 75 * If this takes very long we can split read files 76 * How long takes realign knownsonly (per genome)? 77 * If very long, we need to rewrite workflow 2 to split before realign 78 * For realign: if we split per chromosome, can we also split bam file? 79 * How to easily lift over from b36 to b37 80 * Contact BGI if they can use b37?? 81 82 Todo: 83 84 * Recode workflow 2 to work per genome instead of per chromosome 85 71 86 == List of steps == 72 87