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

A haplotype sharing method for determining the relative age of SNP alleles.

Human heredity - 1 Jan 2010

de Vries André R, te Meerman Gerard J

Abstract excerpt

There are two aspects regarding the age of alleles that are relevant as indicators of the timing of mutational events. The first is to know which alleles are species-specific; the second is about the time of origin of species-specific alleles. Both aspects can be analyzed using haplotype-sharing methods, by using the length of shared haplotypes as a measure of the speed of coalescence to common ancestors. The...

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 Computational Biology
Share to Computer Simulation

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Founder Effect

Share to Genetics, Population

Share to Linkage Disequilibrium

Share to Species Specificity

Share to Time Factors

Source

Identifiers

PMID: 19797909
DOI: 10.1159/000243154

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A haplotype sharing method for determining the relative age of SNP alleles.PMID 19797909Read ↗

Dating genomic variants and shared ancestry in population-scale sequencing dataSemantic proximity Read ↗

Dating genomic variants and shared ancestry in population-scale sequencing data.Semantic proximity Read ↗

Estimating the age of single nucleotide polymorphic sites in humans.Semantic proximity Read ↗

Dating rare mutations from small samples with dense marker data.Semantic proximity Read ↗

Reconstructing the history of founder events using genome-wide patterns of allele sharing across individuals.Semantic proximity Read ↗

Demography and the age of rare variants.Semantic proximity Read ↗

Estimating time to the common ancestor for a beneficial alleleSemantic proximity Read ↗

Estimating Time to the Common Ancestor for a Beneficial Allele.Semantic proximity Read ↗

Haplotype homozygosity and derived alleles in the human genome.Semantic proximity Read ↗

Reconstructing the history of founder events using genome-wide patterns of allele sharing across individualsSemantic proximity Read ↗

Using linked markers to infer the age of a mutation.Semantic proximity Read ↗

Calibrating the Human Mutation Rate via Ancestral Recombination Density in Diploid GenomesSemantic proximity Read ↗

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