SeqArray: Big Data Management of Whole-genome Sequence Variant Calls
Version 1.20.2

Big data management of whole-genome sequencing variant calls with thousands of individuals: genotypic data (e.g., SNVs, indels and structural variation calls) and annotations in SeqArray files are stored in an array-oriented and compressed manner, with efficient data access using the R programming language.

Package details

AuthorXiuwen Zheng [aut, cre], Stephanie Gogarten [aut], David Levine [ctb], Cathy Laurie [ctb]
Bioconductor views DataRepresentation Genetics Infrastructure Sequencing
Date of publication2018-09-10
MaintainerXiuwen Zheng <[email protected]>
Package repositoryView on Bioconductor
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SeqArray documentation built on Sept. 11, 2018, 6 p.m.