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Article

Leveraging multiple genomic data to prioritize disease-causing indels from exome sequencing data.

Scientific reports - 11 May 2017

Wu Mengmeng, Chen Ting, Jiang Rui

Abstract excerpt

The emergence of exome sequencing in recent years has enabled rapid and cost-effective detection of genetic variants in coding regions and offers a great opportunity to combine sequencing experiments with subsequent computational analysis for dissecting genetic basis of human inherited diseases. However, this strategy, though successful in practice, still faces such challenges as limited sample size and...

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Identifiers

PMID: 28496131
DOI: 10.1038/s41598-017-01834-w
PMCID: PMC5431795

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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