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Paper Details

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.
Genome Res
1329
2007
CNV, CNVs, SNP marker, SNPs, copy number variations, human, lymphoblastoid cell lines
Author NameAffiliation
Kai WangUniversity of Pennsylvania
Kai WangUniversity of Pennsylvania
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Release 1.2