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 simple and cost-effective method for rapid genotyping of insertion/deletion polymorphisms.

Genomics - 1 Nov 2003

Robledo Renato, Beggs William, Bender Patrick

Abstract excerpt

We developed a simple method, based on the TaqMan technology, for fast genotyping of insertion/deletion polymorphisms of known location. The genotypes of 22 CEPH individuals, previously ascertained by conventional methods, were confirmed in the new assay without manual, time-consuming, post-PCR analysis. We propose to expand the application of TaqMan probes for population screening of insertion/deletion...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Base Sequence
Share to Costs and Cost Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Probes

Share to Genotype

Share to Mutagenesis, Insertional

Share to Polymorphism, Genetic

Share to Sequence Deletion

Source

Identifiers

PMID: 14559216
DOI: 10.1016/s0888-7543(03)00172-1

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

A simple and cost-effective method for rapid genotyping of insertion/deletion polymorphisms.PMID 14559216Read ↗

TaqMan genotyping of insertion/deletion polymorphisms.Semantic proximity Read ↗

A PCR-based method for detecting rare genotypes in large samples of individuals.Semantic proximity Read ↗

Rapid genotyping of 32 insertion/deletion panel for human identification using fluorogenic probes-based multiplex real-time PCR.Semantic proximity Read ↗

Reliable detection of paternal SNPs within deletion breakpoints for non-invasive prenatal exclusion of homozygous α-thalassemia in maternal plasma.Semantic proximity Read ↗

A Novel Panel of 36 Insertion/Deletion (InDel) Markers for Human IdentificationSemantic proximity Read ↗

High-throughput genotyping of intermediate-size structural variation.Semantic proximity Read ↗

Development of TaqMan allelic discrimination based genotyping of large DNA deletions.Semantic proximity Read ↗

High-Throughput Genotyping with TaqMan Allelic Discrimination and Allele-Specific Genotyping Assays.Semantic proximity Read ↗

Rapid mapping of deletion and duplication mutations by the polymerase chain reaction.Semantic proximity Read ↗

Genotyping using the TaqMan assay.Semantic proximity Read ↗

A simple method to confirm and size deletion, duplication, and insertion mutations detected by sequence analysis.Semantic proximity Read ↗

New tetranucleotide STRP markers for detecting the 22q11.2 deletion.Semantic proximity Read ↗

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