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

Comprehensive human genetic maps: individual and sex-specific variation in recombination.

American journal of human genetics - 1 Sept 1998

Broman K W, Murray J C, Sheffield V C, White R L, Weber J L

Abstract excerpt

Comprehensive human genetic maps were constructed on the basis of nearly 1 million genotypes from eight CEPH families; they incorporated >8,000 short tandem-repeat polymorphisms (STRPs), primarily from Généthon, the Cooperative Human Linkage Center, the Utah Marker Development Group, and the Marshfield Medical Research Foundation. As part of the map building process, 0.08% of the genotypes that resulted in tight...

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 Genetic Markers
Share to Genetic Variation

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

Share to Genome, Human

Share to Genotype

Share to Polymorphism, Genetic

Share to Recombination, Genetic

Share to Repetitive Sequences, Nucleic Acid

Source

Open in PubMed Open full text

Identifiers

PMID: 9718341
DOI: 10.1086/302011
PMCID: PMC1377399

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

Comprehensive human genetic maps: individual and sex-specific variation in recombination.PMID 9718341Read ↗

A high-resolution recombination map of the human genome.Semantic proximity Read ↗

Polymorphic variation in human meiotic recombination.Semantic proximity Read ↗

The CEPH consortium linkage map of human chromosome 1.Semantic proximity Read ↗

Complete human recombination maps.Semantic proximity Read ↗

A familial, telomere-to-telomere reference for human <i>de novo</i> mutation and recombination from a four-generation pedigreeSemantic proximity Read ↗

Sex differences in the genetic basis of human recombination within 190,000 parent-child pairsSemantic proximity Read ↗

The fine-scale structure of recombination rate variation in the human genome.Semantic proximity Read ↗

The 1993-94 Généthon human genetic linkage map.Semantic proximity Read ↗

Systematic Analyses of Autosomal Recombination Rates from the 1000 Genomes Project Uncovers the Global Recombination Landscape in HumansSemantic proximity Read ↗

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC).Semantic proximity Read ↗

Evidence for substantial fine-scale variation in recombination rates across the human genome.Semantic proximity Read ↗

A second-generation combined linkage physical map of the human genome.Semantic proximity Read ↗

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