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

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

BMC bioinformatics - 23 Jun 2008

Yoo Jinho, Lee Youngbok, Kim Yujung, Rha Sun Young, Kim Yangseok

Abstract excerpt

BACKGROUND: Since the completion of the HapMap project, huge numbers of individual genotypes have been generated from many kinds of laboratories. The efforts of finding or interpreting genetic association between disease and SNPs/haplotypes have been on-going widely. So, the necessity of the capability to analyze huge data and diverse interpretation of the results are growing rapidly. RESULTS: We have developed...

Read the complete abstract on PubMed

Topics

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

Share to Algorithms
Share to Data Interpretation, Statistical

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

Share to Genetic Associations and Epidemiology

Share to Haplotypes

Share to Hemoglobinopathies and Related Disorders

Share to Linkage Disequilibrium

Share to Polymorphism, Single Nucleotide

Share to Software

Source

Open in PubMed Open full text

Identifiers

PMID: 18570686
DOI: 10.1186/1471-2105-9-290
PMCID: PMC2453143

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

SNPAnalyzer 2.0: a web-based integrated workbench for linkage disequilibrium analysis and association analysis.PMID 18570686Read ↗

SNPAnalyzer: a web-based integrated workbench for single-nucleotide polymorphism analysis.Semantic proximity Read ↗

A tool for selecting SNPs for association studies based on observed linkage disequilibrium patterns.Semantic proximity Read ↗

Haplo2Ped: a tool using haplotypes as markers for linkage analysis.Semantic proximity Read ↗

LDA--a java-based linkage disequilibrium analyzer.Semantic proximity Read ↗

Selecting single-nucleotide polymorphisms for association studies with SNPbrowser software.Semantic proximity Read ↗

SNPStats: a web tool for the analysis of association studies.Semantic proximity Read ↗

LDkit: a parallel computing toolkit for linkage disequilibrium analysis.Semantic proximity Read ↗

SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci.Semantic proximity Read ↗

LD2SNPing: linkage disequilibrium plotter and RFLP enzyme mining for tag SNPs.Semantic proximity Read ↗

DistiLD Database: diseases and traits in linkage disequilibrium blocks.Semantic proximity Read ↗

SNPHunter: a versatile web-based tool for acquiring and managing single nucleotide polymorphisms.Semantic proximity Read ↗

SNP-PHAGE: high-throughput SNP discovery pipeline.Semantic proximity Read ↗

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