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

Multiplexed shotgun genotyping for rapid and efficient genetic mapping.

Genome research - 1 Apr 2011

Andolfatto Peter, Davison Dan, Erezyilmaz Deniz, Hu Tina T, Mast Joshua, Sunayama-Morita Tomoko, Stern David L

Abstract excerpt

We present a new approach to genotyping based on multiplexed shotgun sequencing that can identify recombination breakpoints in a large number of individuals simultaneously at a resolution sufficient for most mapping purposes, such as quantitative trait locus (QTL) mapping and mapping of induced mutations. We first describe a simple library construction protocol that uses just 10 ng of genomic DNA per individual...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Breakpoints
Share to Computational Biology

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

Share to Drosophila

Share to Genes, Dominant

Share to Molecular Typing

Share to Quantitative Trait Loci

Share to Recombination, Genetic

Share to Research Design

Source

Open in PubMed Open full text

Identifiers

PMID: 21233398
DOI: 10.1101/gr.115402.110
PMCID: PMC3065708

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Multiplexed shotgun genotyping for rapid and efficient genetic mapping.PMID 21233398Read ↗

Population genomics: whole-genome analysis of polymorphism and divergence in Drosophila simulans.Semantic proximity Read ↗

High-throughput 454 resequencing for allele discovery and recombination mapping in Plasmodium falciparum.Semantic proximity Read ↗

Rapid and cost-effective polymorphism identification and genotyping using restriction site associated DNA (RAD) markers.Semantic proximity Read ↗

Mutation mapping and identification by whole-genome sequencing.Semantic proximity Read ↗

Population genomic analysis of model and nonmodel organisms using sequenced RAD tags.Semantic proximity Read ↗

simMSG: an experimental design tool for high-throughput genotyping of hybrids.Semantic proximity Read ↗

SNP discovery and genotyping for evolutionary genetics using RAD sequencing.Semantic proximity Read ↗

Anchor polymerase chain reaction display: a high-throughput method to resolve, score, and isolate dimorphic genetic markers based on interspersed repetitive DNA elements.Semantic proximity Read ↗

Rapid recombination mapping for high-throughput genetic screens in Drosophila.Semantic proximity Read ↗

High-resolution, high-throughput SNP mapping in Drosophila melanogaster.Semantic proximity Read ↗

Rapid SNP discovery and genetic mapping using sequenced RAD markers.Semantic proximity Read ↗

Parent-independent genotyping for constructing an ultrahigh-density linkage map based on population sequencing.Semantic proximity Read ↗

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