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Article

Personalized genomic disease risk of volunteers.

Proceedings of the National Academy of Sciences of the United States of America - 15 Oct 2013

Gonzalez-Garay Manuel L, McGuire Amy L, Pereira Stacey, Caskey C Thomas

Abstract excerpt

Next-generation sequencing (NGS) is commonly used for researching the causes of genetic disorders. However, its usefulness in clinical practice for medical diagnosis is in early development. In this report, we demonstrate the value of NGS for genetic risk assessment and evaluate the limitations a...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 24082139
DOI: 10.1073/pnas.1315934110
PMCID: PMC3801013

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24082139-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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