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Article

Incorporating linkage information into a common disease/rare variant framework.

Genetic epidemiology - 1 Jan 2011

Hinrichs Anthony L, Suarez Brian K

Abstract excerpt

Recent developments in sequencing technology have allowed the investigation of the common disease/rare variant hypothesis. In the Genetic Analysis Workshop 17 data set, we have sequence data on both unrelated individuals and eight large extended pedigrees with simulated quantitative and qualitative phenotypes. Group 11, whose focus was incorporating linkage information, considered several different ways to use...

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Identifiers

PMID: 22128063
DOI: 10.1002/gepi.20654
PMCID: PMC4558895

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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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