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

AncestrySNPminer: a bioinformatics tool to retrieve and develop ancestry informative SNP panels.

Genomics - 1 Jul 2012

Amirisetty Sushil, Hershey Gurjit K Khurana, Baye Tesfaye M

Abstract excerpt

A wealth of genomic information is available in public and private databases. However, this information is underutilized for uncovering population specific and functionally relevant markers underlying complex human traits. Given the huge amount of SNP data available from the annotation of human genetic variation, data mining is a faster and cost effective approach for investigating the number of SNPs that are...

Read the complete abstract on PubMed

Topics

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

Share to Genomics
Share to Algorithms
Share to Databases, Genetic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Markers

Share to Genome, Human

Share to Internet

Share to Population Groups

Share to Software

Source

Open in PubMed Open full text

Identifiers

PMID: 22584067
DOI: 10.1016/j.ygeno.2012.05.003
PMCID: PMC3433799

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

AncestrySNPminer: a bioinformatics tool to retrieve and develop ancestry informative SNP panels.PMID 22584067Read ↗

A standardized framework for representation of ancestry data in genomics studies, with application to the NHGRI-EBI GWAS CatalogSemantic proximity Read ↗

MI-MAAP: marker informativeness for multi-ancestry admixed populations.Semantic proximity Read ↗

Ancestry-informative marker (AIM) SNP panel for the Malay population.Semantic proximity Read ↗

Using the UK Biobank as a global reference of worldwide populations: application to measuring ancestry diversity from GWAS summary statistics.Semantic proximity Read ↗

Ancestry informative markers for fine-scale individual assignment to worldwide populations.Semantic proximity Read ↗

Progress toward an efficient panel of SNPs for ancestry inference.Semantic proximity Read ↗

Softwares and methods for estimating genetic ancestry in human populations.Semantic proximity Read ↗

The Clinical Genome and Ancestry Report: An interactive web application for prioritizing clinically implicated variants from genome sequencing data with ancestry composition.Semantic proximity Read ↗

Fully exploiting SNP arrays: a systematic review on the tools to extract underlying genomic structure.Semantic proximity Read ↗

AEon: A global genetic ancestry estimation toolSemantic proximity Read ↗

SNVstory: inferring genetic ancestry from genome sequencing data.Semantic proximity Read ↗

Efficient analysis of large datasets and sex bias with ADMIXTURESemantic proximity Read ↗

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