(Q29614933)
Statements
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data (English)
Glessner J
1 reference
Wang K
Li M
Hadley D
Liu R
Grant SF
Hakonarson H
Bucan M
November 2007
17
11
1665-74
1 reference