Genome-wide allele screen and chromosome knockout project

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Revision as of 22:37, 5 May 2015 by >YanWu
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Library Design Protocol:

Dry Lab
  1. Input data is either phased haplotypes (in HapCut output format: File:Haplotype.chr21.combine.txt) or SNP Calls in tab delimited format (File:Pgp1 snp calls.tsv, File:HapmapSnpsCEU.txt).
  2. Filter SNP calls or Haploytping data for quality