Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Application of genome-wide SNP data for uncovering pairwise relationships and quantitative trait loci.

Genetica - 1 Jun 2009

Sham P C, Cherny S S, Purcell S

Abstract excerpt

The genetic analysis of quantitative traits in humans is changing as a result of the availability of whole-genome SNP data. Heritability analysis can make use of actual genetic sharing between pairs of individuals estimated from the genotype data, rather than the expected genetic sharing implied by their family relationship. This could provide more accurate heritability estimates and help to overcome the equal...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosome Mapping
Share to Genome, Human
Share to Inheritance Patterns

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pedigree

Share to Polymorphism, Single Nucleotide

Share to Quantitative Trait Loci

Source

Identifiers

PMID: 19127410
DOI: 10.1007/s10709-008-9349-4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Application of genome-wide SNP data for uncovering pairwise relationships and quantitative trait loci.PMID 19127410Read ↗

Relatedness in the post-genomic era: is it still useful?Semantic proximity Read ↗

Statistical methods for genome-wide and sequencing association studies of complex traits in related samples.Semantic proximity Read ↗

Genome-wide complex trait analysis (GCTA): methods, data analyses, and interpretations.Semantic proximity Read ↗

A Weighted SNP Correlation Network Method for Estimating Polygenic Risk Scores.Semantic proximity Read ↗

Genetic mapping of quantitative trait loci for disease-related phenotypes.Semantic proximity Read ↗

SNP discovery in associating genetic variation with human disease phenotypes.Semantic proximity Read ↗

Identity-By-Descent Mapping Using Multi-Individual IBD With Genome-Wide Multiple Testing Adjustment.Semantic proximity Read ↗

Association methods in human genetics.Semantic proximity Read ↗

QTLRel: an R package for genome-wide association studies in which relatedness is a concern.Semantic proximity Read ↗

Localising loci underlying complex trait variation using Regional Genomic Relationship Mapping.Semantic proximity Read ↗

Re-evaluation of SNP heritability in complex human traitsSemantic proximity Read ↗

Analysis of Heritability Using Genome-Wide Data.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.