Making Sense of the Genetic Variations ...
Genetic Variations databases:Entrez SNP: : Genomes: of genomic variants (DGV): : GWAS Catalog: GWAS Catalog: : : mutation databases: PheGenI: Genomic Database (NHGRI): : : : Portal: causing SNPs/Genes:Disease/phenotype centric databases:OMIM: Navigator: Public: : : hsls.Genetic variations in the context of a genomic region:NCBI Map Viewer: Genome Browser: Table Browser: analysis of mutations:Variant Effect Predictor: Genome Trax: Protein: Amino Acid Explorer: Mutation Analyzer:? TMHMM Server: acid properties:? F-SNP: : PolyPhen: SNPs3D: ESE Finder: SPOT: DB: Sciences Library System:InfoBooster: Bioinformatics Resources Collection: —query: “genetic variations” Databases/ToolsArticles on Databases/ToolVideo Tutorials:Identify genetic variations associated with a human disease genetic variations present is a human gene sequence (Part 1) genetic variations present is a human gene sequence (Part 2) all clinically linked Flagged?SNPs?associated with a list of genes (Part1) all clinically linked Flagged?SNPs associated with a list of genes (Part2) Readings:PLOS Computational Biology: Translational Bioinformatics Topics in Genome Analysis: ................
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