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 cost-benefit analysis for use of large SNP panels and high throughput typing for forensic investigative genetic genealogy.

International journal of legal medicine - 1 Sept 2023

Budowle Bruce, Arnette Andrew, Sajantila Antti

Abstract excerpt

Next-generation sequencing (NGS), also known as massively sequencing, enables large dense SNP panel analyses which generate the genetic component of forensic investigative genetic genealogy (FIGG). While the costs of implementing large SNP panel analyses into the laboratory system may seem high and daunting, the benefits of the technology may more than justify the investment. To determine if an infrastructural...

Read the complete abstract on PubMed

Topics

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

Share to Cost-Benefit Analysis
Share to Crime
Share to DNA

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

Share to DNA Fingerprinting

Share to High-Throughput Nucleotide Sequencing

Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 37341834
DOI: 10.1007/s00414-023-03029-7
PMCID: PMC10421786

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 cost-benefit analysis for use of large SNP panels and high throughput typing for forensic investigative genetic genealogy.PMID 37341834Read ↗

SNP assays for DVI: cost, time, and performance information for decision-makersSemantic proximity Read ↗

Review of SNP assays for disaster victim identification: Cost, time, and performance information for decision-makers.Semantic proximity Read ↗

Forensic investigative genetic genealogy based on low-quality DNA whole genome sequencing data.Semantic proximity Read ↗

Law enforcement use of genetic genealogy databases in criminal investigations: Nomenclature, definition and scopeSemantic proximity Read ↗

Policy and regulatory implications of the new frontier of forensic genomics: direct-to-consumer genetic data and genealogy recordsSemantic proximity Read ↗

An empirical investigation into the effectiveness of genetic genealogy to identify individuals in the UK.Semantic proximity Read ↗

Forensic investigative genetic genealogy: expanding pedigree tracing and genetic inquiry in the genomic era.Semantic proximity Read ↗

Investigative genetic genealogy - new approach to detect relatedness of individuals.Semantic proximity Read ↗

Impact of SNP microarray analysis of compromised DNA on kinship classification success in the context of investigative genetic genealogy.Semantic proximity Read ↗

FIGG at 5: An update on U.S. public perspectives on forensic investigative genetic genealogy five years after its introduction to criminal investigationsSemantic proximity Read ↗

Prioritizing privacy and presentation of supportable hypothesis testing in forensic genetic genealogy investigations.Semantic proximity Read ↗

How many single nucleotide polymorphisms (SNPs) are needed to replace short tandem repeats (STRs) in forensic applications?Semantic proximity Read ↗

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