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

Capillary electrophoresis of an 11-plex mtDNA coding region SNP single base extension assay for discrimination of the most common Caucasian HV1/HV2 mitotype.

Methods in molecular biology (Clifton, N.J.) - 1 Jan 2012

Vallone Peter M

Abstract excerpt

The typing of single nucleotide polymorphisms (SNPs) located throughout the human mitochondrial genome assists in resolving individuals with an identical HV1/HV2 haplotype. A set of 11 sites which were selected for distinguishing individuals of a common Western European Caucasian HV1/HV2 mitotype was incorporated into a single base extension (SBE) assay. The assay was optimized for multiplex detection of sequence...

Read the complete abstract on PubMed

Topics

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

Share to Base Pairing
Share to DNA, Mitochondrial

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electrophoresis, Capillary

Share to Mitochondria

Share to Open Reading Frames

Share to Reproducibility of Results

Share to Statistics as Topic

Share to White People

Source

Identifiers

PMID: 22139659
DOI: 10.1007/978-1-61779-461-2_11

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

Capillary electrophoresis of an 11-plex mtDNA coding region SNP single base extension assay for discrimination of the most common Caucasian HV1/HV2 mitotype.PMID 22139659Read ↗

A multiplex allele-specific primer extension assay for forensically informative SNPs distributed throughout the mitochondrial genome.Semantic proximity Read ↗

A rapid mtDNA assay of 22 SNPs in one multiplex reaction increases the power of forensic testing in European Caucasians.Semantic proximity Read ↗

Forensically relevant SNaPshot® assays for human DNA SNP analysis: a review.Semantic proximity Read ↗

Typing of mitochondrial DNA coding region SNPs of forensic and anthropological interest using SNaPshot minisequencing.Semantic proximity Read ↗

Rapid screening of mtDNA coding region SNPs for the identification of west European Caucasian haplogroups.Semantic proximity Read ↗

SNaPshot typing of mitochondrial DNA coding region variants.Semantic proximity Read ↗

SNP genotyping using multiplex single base primer extension assays.Semantic proximity Read ↗

Profiling 627 mitochondrial nucleotides via the analysis of a 23-plex polymerase chain reaction by liquid chromatography-electrospray ionization time-of-flight mass spectrometry.Semantic proximity Read ↗

Multiplex analysis of mitochondrial DNA pathogenic and polymorphic sequence variants.Semantic proximity Read ↗

Detection of 13 Hypervariable Region 1 (Hv1) SNPs using single-base extension (Sbe) primers in parallel with Sanger sequencing.Semantic proximity Read ↗

Development of a new screening method to determine the main 52 mitochondrial haplogroups through a single minisequencing reaction.Semantic proximity Read ↗

HRM and SNaPshot as alternative forensic SNP genotyping methods.Semantic proximity Read ↗

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