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

PopHuman: the human population genomics browser.

Nucleic acids research - 4 Jan 2018

Casillas Sònia, Mulet Roger, Villegas-Mirón Pablo, Hervas Sergi, Sanz Esteve, Velasco Daniel, Bertranpetit Jaume, Laayouni Hafid, Barbadilla Antonio

Abstract excerpt

The 1000 Genomes Project (1000GP) represents the most comprehensive world-wide nucleotide variation data set so far in humans, providing the sequencing and analysis of 2504 genomes from 26 populations and reporting >84 million variants. The availability of this sequence data provides the human lineage with an invaluable resource for population genomics studies, allowing the testing of molecular population...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human
Share to Databases, Genetic

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

Share to Genetic Variation

Share to Genetics, Population

Share to Genome, Human

Share to Genomics

Source

Open in PubMed Open full text

Identifiers

PMID: 29059408
DOI: 10.1093/nar/gkx943
PMCID: PMC5753332

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

PopHuman: the human population genomics browser.PMID 29059408Read ↗

PGG.Population: a database for understanding the genomic diversity and genetic ancestry of human populations.Semantic proximity Read ↗

PopFly: the Drosophila population genomics browser.Semantic proximity Read ↗

Insights into human genetic variation and population history from 929 diverse genomesSemantic proximity Read ↗

Insights into human genetic variation and population history from 929 diverse genomes.Semantic proximity Read ↗

PopDrowser: the Population Drosophila Browser.Semantic proximity Read ↗

Population genomics: a bridge from evolutionary history to genetic medicine.Semantic proximity Read ↗

PopHumanVar: an interactive application for the functional characterization and prioritization of adaptive genomic variants in humans.Semantic proximity Read ↗

PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.Semantic proximity Read ↗

Bayesian inference of ancient human demography from individual genome sequences.Semantic proximity Read ↗

Population genetic inference from personal genome data: impact of ancestry and admixture on human genomic variation.Semantic proximity Read ↗

PopGenome: an efficient Swiss army knife for population genomic analyses in R.Semantic proximity Read ↗

Demographic history and rare allele sharing among human populations.Semantic proximity Read ↗

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