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

DistiLD Database: diseases and traits in linkage disequilibrium blocks.

Nucleic acids research - 1 Jan 2012

Pallejà Albert, Horn Heiko, Eliasson Sabrina, Jensen Lars Juhl

Abstract excerpt

Genome-wide association studies (GWAS) have identified thousands of single nucleotide polymorphisms (SNPs) associated with the risk of hundreds of diseases. However, there is currently no database that enables non-specialists to answer the following simple questions: which SNPs associated with diseases are in linkage disequilibrium (LD) with a gene of interest? Which chromosomal regions have been associated with...

Read the complete abstract on PubMed

Topics

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

Share to Databases, Nucleic Acid
Share to Disease
Share to Genome-Wide Association Study

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

Share to Linkage Disequilibrium

Share to Molecular Sequence Annotation

Share to Polymorphism, Single Nucleotide

Share to User-Computer Interface

Source

Open in PubMed Open full text

Identifiers

PMID: 22058129
DOI: 10.1093/nar/gkr899
PMCID: PMC3245128

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

DistiLD Database: diseases and traits in linkage disequilibrium blocks.PMID 22058129Read ↗

LDGIdb: a database of gene interactions inferred from long-range strong linkage disequilibrium between pairs of SNPs.Semantic proximity Read ↗

Ancestry-specific maps of GRCh38 linkage disequilibrium blocks for human genome researchSemantic proximity Read ↗

LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants.Semantic proximity Read ↗

LDMAP: the construction of high-resolution linkage disequilibrium maps of the human genome.Semantic proximity Read ↗

Assessing the patterns of linkage disequilibrium in genic regions of the human genome.Semantic proximity Read ↗

GWASdb: a database for human genetic variants identified by genome-wide association studies.Semantic proximity Read ↗

snpXplorer: an interactive platform for haplotype-aware exploration and integrated annotation of GWAS dataSemantic proximity Read ↗

Structural Variants in Linkage Disequilibrium with GWAS-Significant SNPsSemantic proximity Read ↗

LDtrait: An Online Tool for Identifying Published Phenotype Associations in Linkage Disequilibrium.Semantic proximity Read ↗

CAUSALdb2: an updated database for causal variants of complex traits.Semantic proximity Read ↗

DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation.Semantic proximity Read ↗

SNPAnalyzer 2.0: a web-based integrated workbench for linkage disequilibrium analysis and association analysis.Semantic proximity Read ↗

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