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Article

Designing deep sequencing experiments: detecting structural variation and estimating transcript abundance.

BMC genomics - 18 Jun 2010

Bashir Ali, Bansal Vikas, Bafna Vineet

Abstract excerpt

BACKGROUND: Massively parallel DNA sequencing technologies have enabled the sequencing of several individual human genomes. These technologies are also being used in novel ways for mRNA expression profiling, genome-wide discovery of transcription-factor binding sites, small RNA discovery, etc. Th...

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PMID: 20565853
DOI: 10.1186/1471-2164-11-385
PMCID: PMC3091630

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20565853-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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