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...

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Detalles Bibliográficos
Autores principales: Wang, Xihong, Zheng, Zhuqing, Cai, Yudong, Chen, Ting, Li, Chao, Fu, Weiwei, Jiang, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Technical Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5751039/
https://www.ncbi.nlm.nih.gov/pubmed/29220491
http://dx.doi.org/10.1093/gigascience/gix115

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5751039/
https://www.ncbi.nlm.nih.gov/pubmed/29220491
http://dx.doi.org/10.1093/gigascience/gix115

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