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

Evaluation of the Precision ID Ancestry Panel for crime case work: A SNP typing assay developed for typing of 165 ancestral informative markers.

Forensic science international. Genetics - 1 May 2017

Pereira Vania, Mogensen Helle S, Børsting Claus, Morling Niels

Abstract excerpt

The application of massive parallel sequencing (MPS) methodologies in forensic genetics is promising and it is gradually being implemented in forensic genetic case work. One of the major advantages of these technologies is that several traditional electrophoresis assays can be combined into one single MPS assay. This reduces both the amount of sample used and the time of the investigations. This study assessed...

Read the complete abstract on PubMed

Topics

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

Share to Denmark
Share to Forensic Genetics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Markers

Share to Genetics, Population

Share to Genotyping Techniques

Share to Heterozygote

Share to High-Throughput Nucleotide Sequencing

Share to Racial Groups

Source

Identifiers

PMID: 28273506
DOI: 10.1016/j.fsigen.2017.02.013

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

Evaluation of the Precision ID Ancestry Panel for crime case work: A SNP typing assay developed for typing of 165 ancestral informative markers.PMID 28273506Read ↗

Assessment of the Precision ID Ancestry panel.Semantic proximity Read ↗

An alternate workflow for preparing Precision ID Ancestry and Identity Panel libraries for Illumina sequencing.Semantic proximity Read ↗

Frequencies of the precision ID ancestry panel markers in Basques using the Ion Torrent PGMTM platform.Semantic proximity Read ↗

Evaluation of the Ion AmpliSeq™ PhenoTrivium Panel: MPS-Based Assay for Ancestry and Phenotype Predictions Challenged by Casework Samples.Semantic proximity Read ↗

Inference of Ancestry in Forensic Analysis II: Analysis of Genetic Data.Semantic proximity Read ↗

Applications and Performance of Precision ID GlobalFiler NGS STR, Identity, and Ancestry Panels in Forensic Genetics.Semantic proximity Read ↗

Forensically relevant SNP classes.Semantic proximity Read ↗

Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™.Semantic proximity Read ↗

Comparative evaluation of the MAPlex, Precision ID Ancestry Panel, and VISAGE Basic Tool for biogeographical ancestry inference.Semantic proximity Read ↗

Evaluation of a custom QIAseq targeted DNA panel with 164 ancestry informative markers sequenced with the Illumina MiSeq.Semantic proximity Read ↗

Massively parallel sequencing of 124 SNPs included in the precision ID identity panel in three East Asian minority ethnicities.Semantic proximity Read ↗

A 34-plex autosomal SNP single base extension assay for ancestry investigations.Semantic proximity Read ↗

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