![](/img/cover-not-exists.png)
PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
Wang, K., Li, M., Hadley, D., Liu, R., Glessner, J., Grant, S. F.A., Hakonarson, H., Bucan, M.Volume:
17
Language:
english
Journal:
Genome Research
DOI:
10.1101/gr.6861907
Date:
November, 2007
File:
PDF, 1.06 MB
english, 2007