Cite
HARVARD Citation
Suvakov, M. et al. (2021). CNVpytor: a tool for copy number variation detection and analysis from read depth and allele imbalance in whole-genome sequencing. GigaScience. 10 (11), p. . [Online].
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Suvakov, M. et al. (2021). CNVpytor: a tool for copy number variation detection and analysis from read depth and allele imbalance in whole-genome sequencing. GigaScience. 10 (11), p. . [Online].