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 454 multiplex sequencing method for rapid and reliable genotyping of highly polymorphic genes in large-scale studies.

BMC genomics - 11 May 2010

Galan Maxime, Guivier Emmanuel, Caraux Gilles, Charbonnel Nathalie, Cosson Jean-François

Abstract excerpt

BACKGROUND: High-throughput sequencing technologies offer new perspectives for biomedical, agronomical and evolutionary research. Promising progresses now concern the application of these technologies to large-scale studies of genetic variation. Such studies require the genotyping of high numbers of samples. This is theoretically possible using 454 pyrosequencing, which generates billions of base pairs of...

Read the complete abstract on PubMed

Topics

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

Share to Genotype
Share to Lung
Share to Reproducibility of Results

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

Share to Rodentia

Share to Sequence Analysis, DNA

Source

Open in PubMed Open full text

Identifiers

PMID: 20459828
DOI: 10.1186/1471-2164-11-296
PMCID: PMC2876125

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 454 multiplex sequencing method for rapid and reliable genotyping of highly polymorphic genes in large-scale studies.PMID 20459828Read ↗

Pyrosequencing: an accurate detection platform for single nucleotide polymorphisms.Semantic proximity Read ↗

Efficient high-throughput resequencing of genomic DNA.Semantic proximity Read ↗

MIG-seq: an effective PCR-based method for genome-wide single-nucleotide polymorphism genotyping using the next-generation sequencing platform.Semantic proximity Read ↗

Double digest RADseq: an inexpensive method for de novo SNP discovery and genotyping in model and non-model species.Semantic proximity Read ↗

Molecular haplotype determination using allele-specific PCR and pyrosequencing technology.Semantic proximity Read ↗

Ultra-high resolution HLA genotyping and allele discovery by highly multiplexed cDNA amplicon pyrosequencing.Semantic proximity Read ↗

Pyrosequencing AB.Semantic proximity Read ↗

Evaluation of human gene variant detection in amplicon pools by the GS-FLX parallel Pyrosequencer.Semantic proximity Read ↗

Genetic variation analyses by Pyrosequencing.Semantic proximity Read ↗

Pyrosequencing for SNP genotyping.Semantic proximity Read ↗

SNP discovery and allele frequency estimation by deep sequencing of reduced representation libraries.Semantic proximity Read ↗

A Kmer-based paired-end read (KPR) <i>de novo</i> assembler and genotyper to genotype major histocompatibility complex class I (MHC-I) alleles for the dogSemantic proximity Read ↗

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