Article

Extracting allelic read counts from 250,000 human sequencing runs in Sequence Read Archive

2018-08-07

Abstract excerpt

The Sequence Read Archive (SRA) contains over one million publicly available sequencing runs from various studies using a variety of sequencing library strategies. These data inherently contain information about underlying genomic sequence variants which we exploit to extract allelic read counts on an unprecedented scale. We reprocessed over 250,000 human sequencing runs (>1000 TB data worth of raw sequence data)...

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Literature Corpus work: 07bcf4c5-8ab7-5912-afbb-9b838a25a8d1
DOI: 10.1101/386441

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