mcshane/hapdip
The CHM1-NA12878 benchmark for single-sample SNP/INDEL calling from WGS Illumina data
64,976 whole genome haplotypes from the Haplotype Reference Consortium and efficient algorithms to use them
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The CHM1-NA12878 benchmark for single-sample SNP/INDEL calling from WGS Illumina data
Public repository.
tools for working with variant graphs
Detect truncation of BGZF files by checking the EOF marker exists