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

Validation of a 21-locus autosomal SNP multiplex for forensic identification purposes.

Forensic science international - 10 Nov 2005

Dixon L A, Murray C M, Archer E J, Dobbins A E, Koumi P, Gill P

Abstract excerpt

A single nucleotide polymorphism (SNP) multiplex has been developed to analyse highly degraded and low copy number (LCN) DNA template, i.e. <100 pg, for scenarios including mass disaster identification. The multiplex consists of 20 autosomal non-coding loci plus Amelogenin for sex determination, amplified in a single tube PCR reaction and visualised on the Applied Biosystems 3100 capillary electrophoresis (CE)...

Read the complete abstract on PubMed

Topics

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

Share to Amelogenin
Share to Blood Chemical Analysis
Share to Dental Enamel Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electrophoresis, Capillary

Share to Racial Groups

Share to Saliva

Share to Sex Determination Analysis

Source

Identifiers

PMID: 16182950
DOI: 10.1016/j.forsciint.2004.12.011

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

Validation of a 21-locus autosomal SNP multiplex for forensic identification purposes.PMID 16182950Read ↗

Autosomal SNP typing of forensic samples with the GenPlex™ HID System: results of a collaborative study.Semantic proximity Read ↗

Developing multiplexed SNP assays with special reference to degraded DNA templates.Semantic proximity Read ↗

Development and validation of a STR and SNP multiplex detection system (88 STRs and 348 SNPs) using massively parallel sequencing.Semantic proximity Read ↗

Development and validation of a novel multiplexed DNA analysis system, InnoTyper® 21.Semantic proximity Read ↗

Forensic validation of the SNPforID 52-plex assay.Semantic proximity Read ↗

Typing of 49 autosomal SNPs by single base extension and capillary electrophoresis for forensic genetic testing.Semantic proximity Read ↗

Systematic evaluation of the Precision ID GlobalFiler™ NGS STR panel v2 using single-source samples of various quantity and quality and mixed DNA samples.Semantic proximity Read ↗

Forensic performance of two insertion-deletion marker assays.Semantic proximity Read ↗

Internal validation of the Mini25A system: The six-dyes labelled kit for forensic degraded samples.Semantic proximity Read ↗

STRs, mini STRs and SNPs--a comparative study for typing degraded DNA.Semantic proximity Read ↗

Analyzing degraded DNA and challenging samples using the ForenSeq™ DNA Signature Prep kit.Semantic proximity Read ↗

Qualitative and quantitative assessment of Illumina's forensic STR and SNP kits on MiSeq FGx™.Semantic proximity Read ↗

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