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

Lost in the space of bioinformatic tools: a constantly updated survival guide for genetic epidemiology. The GenEpi Toolbox.

Atherosclerosis - 1 Apr 2010

Coassin Stefan, Brandstätter Anita, Kronenberg Florian

Abstract excerpt

Genome-wide association studies (GWASs) led to impressive advances in the elucidation of genetic factors underlying complex phenotypes and diseases. However, the ability of GWAS to identify new susceptibility loci in a hypothesis-free approach requires tools to quickly retrieve comprehensive information about a genomic region and analyze the potential effects of coding and non-coding SNPs in a candidate gene...

Read the complete abstract on PubMed

Topics

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

Share to Computational Biology
Share to Data Mining
Share to Databases, Genetic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Decision Trees

Share to Genome, Human

Share to MicroRNAs

Share to Molecular Epidemiology

Share to Software

Source

Identifiers

PMID: 19963217
DOI: 10.1016/j.atherosclerosis.2009.10.026

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

Lost in the space of bioinformatic tools: a constantly updated survival guide for genetic epidemiology. The GenEpi Toolbox.PMID 19963217Read ↗

Genetic variation analysis for biomedical researchers: a primer.Semantic proximity Read ↗

pfSNP: An integrated potentially functional SNP resource that facilitates hypotheses generation through knowledge syntheses.Semantic proximity Read ↗

Demystifying non-coding GWAS variants: an overview of computational tools and methods.Semantic proximity Read ↗

In silico gene discovery.Semantic proximity Read ↗

Role of in silico tools in gene discovery.Semantic proximity Read ↗

From Identification to Function: Current Strategies to Prioritise and Follow-Up GWAS Results.Semantic proximity Read ↗

A systematic approach to understand the functional consequences of non-protein coding risk regions.Semantic proximity Read ↗

Genetic study of complex diseases in the post-GWAS era.Semantic proximity Read ↗

Challenges and progress in interpretation of non-coding genetic variants associated with human disease.Semantic proximity Read ↗

Genetics for clinicians: from candidate genes to whole genome scans (technological advances).Semantic proximity Read ↗

Bioinformatic tools for identifying disease gene and SNP candidates.Semantic proximity Read ↗

Role of genetic variability in Mendelian and multifactorial diseases.Semantic proximity Read ↗

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