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Article

GenomeVIP: a cloud platform for genomic variant discovery and interpretation.

Genome research - 1 Aug 2017

Mashl R Jay, Scott Adam D, Huang Kuan-Lin, Wyczalkowski Matthew A, Yoon Christopher J, Niu Beifang, DeNardo Erin, Yellapantula Venkata D, Handsaker Robert E, Chen Ken, Koboldt Daniel C, Ye Kai, Fenyö David, Raphael Benjamin J, Wendl Michael C, Ding Li

Abstract excerpt

Identifying genomic variants is a fundamental first step toward the understanding of the role of inherited and acquired variation in disease. The accelerating growth in the corpus of sequencing data that underpins such analysis is making the data-download bottleneck more evident, placing substantial burdens on the research community to keep pace. As a result, the search for alternative approaches to the...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 28522612
DOI: 10.1101/gr.211656.116
PMCID: PMC5538560

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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