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

Methods in molecular biology (Clifton, N.J.) - 1 Jan 2007

Niu Tianhua

Abstract excerpt

Sites in the DNA sequences where two homologous chromosomes differ at a single DNA base are called single nucleotide polymorphisms (SNPs). The human genome contains at least 10 million SNPs, making them the most abundant genetic "lampposts" for pinpointing causal variants underlying human diseases. SNP-related toolboxes and databases have become increasingly important for researchers to choose the most...

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PMID: 18025704
DOI: 10.1007/978-1-59745-515-2_23

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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.

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SNPHunter: a versatile web-based tool for acquiring and managing single nucleotide polymorphisms.PMID 18025704Read ↗

SNPHunter: a bioinformatic software for single nucleotide polymorphism data acquisition and management.Semantic proximity Read ↗

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A web-based tool to retrieve human genome polymorphisms from public databases.Semantic proximity Read ↗

SNPper: retrieval and analysis of human SNPs.Semantic proximity Read ↗

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

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

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms.Semantic proximity Read ↗

LS-SNP: large-scale annotation of coding non-synonymous SNPs based on multiple information sources.Semantic proximity Read ↗

SNPServer: a real-time SNP discovery tool.Semantic proximity Read ↗

METU-SNP: an integrated software system for SNP-complex disease association analysis.Semantic proximity Read ↗

PhD-SNPg: a webserver and lightweight tool for scoring single nucleotide variants.Semantic proximity Read ↗

NGS_SNPAnalyzer: a desktop software supporting genome projects by identifying and visualizing sequence variations from next-generation sequencing data.Semantic proximity Read ↗

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