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

VarRanker: rapid prioritization of sequence variations associated with human disease.

BMC bioinformatics - 1 Jan 2013

O'Fallon Brendan D, Wooderchak-Donahue Whitney, Bayrak-Toydemir Pinar, Crockett David

Abstract excerpt

BACKGROUND: Identification of the genetic alterations responsible for human disease is a central challenge facing medical genetics. While many algorithms have been developed to predict the degree of damage caused by a given sequence alteration, few tools are able to incorporate information about a given phenotype of interest. METHODS: Here, we describe an algorithm and web-based application which take into...

Read the complete abstract on PubMed

Topics

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

Share to Algorithms
Share to Anemia, Diamond-Blackfan
Share to Genomic Structural Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Information Storage and Retrieval

Share to Linear Models

Share to Sequence Analysis, Protein

Share to Telangiectasia, Hereditary Hemorrhagic

Share to Vocabulary, Controlled

Source

Open in PubMed Open full text

Identifiers

PMID: 24268183
DOI: 10.1186/1471-2105-14-S13-S1
PMCID: PMC3849749

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 · 11 closest

VarRanker: rapid prioritization of sequence variations associated with human disease.PMID 24268183Read ↗

MetaRanker 2.0: a web server for prioritization of genetic variation data.Semantic proximity Read ↗

Variant Ranker: a web-tool to rank genomic data according to functional significance.Semantic proximity Read ↗

Prioritizing regions of candidate genes for efficient mutation screening.Semantic proximity Read ↗

Speeding disease gene discovery by sequence based candidate prioritization.Semantic proximity Read ↗

Web tools for the prioritization of candidate disease genes.Semantic proximity Read ↗

HitWalker: variant prioritization for personalized functional cancer genomics.Semantic proximity Read ↗

Candidate gene prioritization.Semantic proximity Read ↗

SNPranker 2.0: a gene-centric data mining tool for diseases associated SNP prioritization in GWAS.Semantic proximity Read ↗

SNPRanker: a tool for identification and scoring of SNPs associated to target genes.Semantic proximity Read ↗

Comparison of vocabularies, representations and ranking algorithms for gene prioritization by text mining.Semantic proximity Read ↗

In silico molecular cytogenetics: a bioinformatic approach to prioritization of candidate genes and copy number variations for basic and clinical genome researchSemantic proximity Read ↗

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