CNVcaller: highly efficient and widely applicable software for detecting copy number variations in large populations

BACKGROUND: The increasing amount of sequencing data available for a wide variety of species can be theoretically used for detecting copy number variations (CNVs) at the population level. However, the growing sample sizes and the divergent complexity of nonhuman genomes challenge the efficiency and...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Gigascience
Egile Nagusiak: Wang, Xihong, Zheng, Zhuqing, Cai, Yudong, Chen, Ting, Li, Chao, Fu, Weiwei, Jiang, Yu
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2017
Gaiak:
Technical Note
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5751039/
https://ncbi.nlm.nih.gov/pubmed/29220491
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/gigascience/gix115
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