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

SUSPECTS: enabling fast and effective prioritization of positional candidates.

Bioinformatics (Oxford, England) - 15 Mar 2006

Adie E A, Adams R R, Evans K L, Porteous D J, Pickard B S

Abstract excerpt

UNLABELLED: SUSPECTS is a web-based server which combines annotation and sequence-based approaches to prioritize disease candidate genes in large regions of interest. It uses multiple lines of evidence to rank genes quickly and effectively while limiting the effect of annotation bias to significantly improve performance. AVAILABILITY: SUSPECTS is freely available at http://www.genetics.med.ed.ac.uk/suspects/...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Mapping
Share to Genetic Markers
Share to Genetic Predisposition to Disease

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

Share to Genetic Testing

Share to Internet

Share to Sequence Analysis, DNA

Share to Software

Share to User-Computer Interface

Source

Identifiers

PMID: 16423925
DOI: 10.1093/bioinformatics/btk031

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

SUSPECTS: enabling fast and effective prioritization of positional candidates.PMID 16423925Read ↗

Prioritization of positional candidate genes using multiple web-based software tools.Semantic proximity Read ↗

POCUS: mining genomic sequence annotation to predict disease genes.Semantic proximity Read ↗

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

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

Candidate gene discovery and prioritization in rare diseases.Semantic proximity Read ↗

Candidate gene prioritization.Semantic proximity Read ↗

Computational tools for prioritizing candidate genes: boosting disease gene discovery.Semantic proximity Read ↗

Candidate gene prioritization with Endeavour.Semantic proximity Read ↗

Computational approaches for human disease gene prediction and ranking.Semantic proximity Read ↗

Gene Prospector: an evidence gateway for evaluating potential susceptibility genes and interacting risk factors for human diseases.Semantic proximity Read ↗

Recent approaches to the prioritization of candidate disease genes.Semantic proximity Read ↗

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

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