ATAV: a comprehensive platform for population-scale genomic analyses

BACKGROUND: A common approach for sequencing studies is to do joint-calling and store variants of all samples in a single file. If new samples are continually added or controls are re-used for several studies, the cost and time required to perform joint-calling for each analysis can become prohibiti...

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Detalles Bibliográficos
Autores principales: Ren, Zhong, Povysil, Gundula, Hostyk, Joseph A., Cui, Hongzhu, Bhardwaj, Nitin, Goldstein, David B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988908/
https://www.ncbi.nlm.nih.gov/pubmed/33757430
http://dx.doi.org/10.1186/s12859-021-04071-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988908/
https://www.ncbi.nlm.nih.gov/pubmed/33757430
http://dx.doi.org/10.1186/s12859-021-04071-1

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