Genomics

These links provide up-to-date and relevant information for genomic researchers.

Found 19 links

Displaying 15 links

DIANA-microTTool Content

http://www.microrna.gr/microT

The DIANA-microT web server predicts targets for miRNAs and provides functional information on the predicted miRNA:target gene interaction from various online biological resources. Updates enable the association of miRNAs to diseases through bibliographic analysis and connection to the UCSC genome browser.

GendooTool Content

http://gendoo.dbcls.jp

Gene Disease Features Ontology-based Overview System (Gendoo) is a web tool for visualizing disease feature profiles generated from the assignment of MeSH vocabulary for associated drugs, biological phenomena and anatomy to OMIM data. This approach assists in interpreting -omic data for its molecular and clinical aspects.

This content is being maintained by thecla.

GeneMANIATool Content

http://www.genemania.org

GeneMANIA is web interface for generating hypotheses about gene function, analyzing gene lists and prioritizing genes for functional assays. Users input a query list for extension and weighting with functionally similar genes. Six organisms are supported.

This content is being maintained by baderg.

Genome HubResource Content

http://www.genome.gov/10000375

Lists of genome-related sites maintained by the NHGRI on behalf of the International Human Genome Sequencing Consortium.

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GSA-SNPTool Content

http://gsa.muldas.org

GSA-SNP web server performs gene set analysis (GSA) on genome-wide association data, using 3 different GSA methods.

Human Genome Variation NomenclatureResource Content

http://www.hgvs.org/rec.html

The Human Genome Society has established a committee to suggest standards for the description of sequence variants in DNA, RNA, and protein sequences. The standards are linked here.

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i-GSEA4GWASTool Content

http://gsea4gwas.psych.ac.cn

i-GSEA4GWAS is a web server for identification of pathways and gene sets associated with traits. An improved gene set enrichment analysis (i-GSEA) is applied to genome wide association studies (GWAS).

ICSNPathwayTool Content

http://icsnpathway.psych.ac.cn/

ICSNPathway is a web tool for the identification of candidate causal SNPs and their corresponding candidate causal pathways from genome wide association studies. ISCNPathway integrates linkage disequilibrium analysis, functional SNP annotation and pathway based analysis to identify these SNPs and pathways.

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IGGTool Content

http://bioinfo.hku.hk:13080/iggweb/

Integration of Genotypes from Genechips (IGG) is a Java-based tool with graphic interface to integrate genotypes across high throughput genotyping platforms from Affymetrix and Illumina and the HapMap Project. It is equipped with a series of functions to control qualities of genotype integration and to flexibly export genotypes for genetic studies as well.

INTERFEROMEDatabase Content

http://www.interferome.org/

INTERFEROME is an open access database of types I, II and III Interferon regulated genes collected from analysing expression data sets of cells treated with IFNs. This database integrates expression information with annotation, ontology, orthologue sequences from 37 species, tissue expression patterns and gene regulatory information.

mirToolsTool Content

http://centre.bioinformatics.zj.cn/mirtools/

mirTools allows users to comprehensively characterize the small RNA transcriptome from high-throughput sequencing data. Users can filter quality reads, align short reads to the reference genome, classify small RNA candidates into known miRNAs, non-coding RNA, genomic repeats, etc. among other analysis tools.

MMIATool Content

http://cancer.informatics.indiana.edu/mmia

microRNA and mRNA Integrated Analysis (MMIA) is a web server that integrates miRNA and mRNA expression data with predicted miRNA target information. MMIA incorporates miRNA prediction algorithms (TargetScan, PITA, PicTar).

MutalyzerTool Content

http://www.mutalyzer.nl/

Mutalyzer was primarily developed to check the description of sequence variants identified in a gene during genetic testing according to the rules of the standard human sequence variant nomenclature of the Human Genome Variation Society. The Mutalyzer 2 parser is based on a formalized description of the nomenclature in Extended Backus-Naur Form. Mutalyzer applies the nomenclature rules and corrects variant descriptions accordingly.

This content is being maintained by P.Taschner.