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fitSNPs Server - Functionally interpolating Single Nucleotide Polymorphism

Differentially expressed genes were more likely to have disease-associated variantsBased on this property, we derived a list of functionally interpolating SNPs (fitSNPs) to prioritize genes for disease association.Human genes have disease-associated variants along with experimently confirmed disease association.GAD.OMIM.Differential expression ratios (DER).UCSC genome graph.GWAS data.

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fitSNPs Server - Functionally interpolating Single Nucleotide Polymorphism | fitsnps.stanford.edu Reviews
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Differentially expressed genes were more likely to have disease-associated variantsBased on this property, we derived a list of functionally interpolating SNPs (fitSNPs) to prioritize genes for disease association.Human genes have disease-associated variants along with experimently confirmed disease association.GAD.OMIM.Differential expression ratios (DER).UCSC genome graph.GWAS data.
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2 Gene prioritization
3 single nucleotide polymorphism
4 disease
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fitSNPs Server - Functionally interpolating Single Nucleotide Polymorphism | fitsnps.stanford.edu Reviews

https://fitsnps.stanford.edu

Differentially expressed genes were more likely to have disease-associated variantsBased on this property, we derived a list of functionally interpolating SNPs (fitSNPs) to prioritize genes for disease association.Human genes have disease-associated variants along with experimently confirmed disease association.GAD.OMIM.Differential expression ratios (DER).UCSC genome graph.GWAS data.

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fitSNPs Server - Functionally interpolating Single Nucleotide Polymorphism

Page describes a simple step-by-step tutorial to load fitSNPs into UCSC genome graph and visualize it along with your genomic data, such as GWAS data. Some highly differentially expressed genes have not yet been associated with any disease, and are interesting investigative leads. We used fitSNPs to prioritize genes for diseases with previously identified loci and unknown molecular basis from OMIM, and suggested 2586 genes to be sequenced for 597 syndromes in the prediction. Last updated on May 14 , 2009.

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