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

Expression-based genetic/physical maps of single-nucleotide polymorphisms identified by the cancer genome anatomy project.

Genome research - 1 Aug 2000

Clifford R, Edmonson M, Hu Y, Nguyen C, Scherpbier T, Buetow K H

Abstract excerpt

SNPs (Single-Nucleotide Polymorphisms), the most common DNA variant in humans, represent a valuable resource for the genetic analysis of cancer and other illnesses. These markers may be used in a variety of ways to investigate the genetic underpinnings of disease. In gene-based studies, the correlations between allelic variants of genes of interest and particular disease states are assessed. An extensive...

Read the complete abstract on PubMed

Topics

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

Share to Databases, Factual
Share to Gene Library
Share to Human Genome Project

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Information Storage and Retrieval

Share to Internet

Share to Physical Chromosome Mapping

Share to Reproducibility of Results

Share to Software

Source

Open in PubMed Open full text

Identifiers

PMID: 10958644
DOI: 10.1101/gr.10.8.1259
PMCID: PMC310932

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

Expression-based genetic/physical maps of single-nucleotide polymorphisms identified by the cancer genome anatomy project.PMID 10958644Read ↗

SNPnotes: high-throughput tissue-specific functional annotation of single nucleotide variantsSemantic proximity Read ↗

Where in the genome are significant single nucleotide polymorphisms from genome-wide association studies located?Semantic proximity Read ↗

Single nucleotide polymorphisms in clinics: Fantasy or reality for cancer?Semantic proximity Read ↗

A practical guide for the functional annotation of genetic variations using SNPnexus.Semantic proximity Read ↗

Bioinformatics tools for single nucleotide polymorphism discovery and analysis.Semantic proximity Read ↗

Genome and genetic resources from the Cancer Genome Anatomy Project.Semantic proximity Read ↗

High-throughput SNP analysis for genetic association studies.Semantic proximity Read ↗

SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes.Semantic proximity Read ↗

SNPLogic: an interactive single nucleotide polymorphism selection, annotation, and prioritization system.Semantic proximity Read ↗

SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies.Semantic proximity Read ↗

A new cancer genome anatomy project web resource for the community.Semantic proximity Read ↗

Expression and Genetic Variation Databases for Cancer ResearchSemantic proximity Read ↗

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