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SNPs@BioFolD

In this page are reported information about the projects related to the annotation of the impact of Single Nucleotide Variants (SNVs) on human health. Currently we have four available web tools located in our server:. Support Vector Machine based method to discriminate between neutral or disease-related single point protein mutations. Meta-predictor of disease causing variants that uses the output of PANTHER, PhD-SNP, SIFT and SNAP.

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SNPs@BioFolD | snps.biofold.org Reviews
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In this page are reported information about the projects related to the annotation of the impact of Single Nucleotide Variants (SNVs) on human health. Currently we have four available web tools located in our server:. Support Vector Machine based method to discriminate between neutral or disease-related single point protein mutations. Meta-predictor of disease causing variants that uses the output of PANTHER, PhD-SNP, SIFT and SNAP.
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2 folding
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7 I-Mutant
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10 SNPs&GO
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SNPs@BioFolD | snps.biofold.org Reviews

https://snps.biofold.org

In this page are reported information about the projects related to the annotation of the impact of Single Nucleotide Variants (SNVs) on human health. Currently we have four available web tools located in our server:. Support Vector Machine based method to discriminate between neutral or disease-related single point protein mutations. Meta-predictor of disease causing variants that uses the output of PANTHER, PhD-SNP, SIFT and SNAP.

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snps.biofold.org snps.biofold.org
1

Mut2Dis Project @ Structural Bioinformatics Unit

http://snps.biofold.org/mut2dis/index.html

Marie-Curie International Outgoing Fellowship. New methods to evaluate the impact of single point protein mutation on human health. Outgoing Phase at the Stanford University (24 months) - Periodic Report 1. Returning Phase at the University of Balearic Islands (12 months) - Periodic Report 2. European Union. Marie Curie Action. 2009-2012 [IOF-237225] New methods to evaluate the impact of single point protein mutation on human health.

2

Emidio Capriotti - BioFolD - Publications

http://snps.biofold.org/pages/papers.html

Capriotti E, Martelli PL, Fariselli P, Casadio R. 2017) Blind prediction of deleterious amino acid variations with SNPs&GO. Human Mutation. Khass M, Blackburn T, Burrows PD, Walter MR, Capriotti E, Schroeder HW Jr. 2016) VpreB serves as an invariant surrogate antigen for selecting immunoglobulin antigen-binding sites. Science Immunology. Tian R, Basu MK, Capriotti E. 2015) Computational methods and resources for the interpretation of genomic variants in cancer. BMC Genomics. 16 (Suppl. 8): S7. 2013) WebR...

3

Emidio Capriotti - BioFolD - Resources

http://snps.biofold.org/pages/resources.html

The researchers of the BioFolD Unit have developed several web server applications that are currently hosted on servers of the Institute for Mathematical Modeling of Biological Systems, University of Düsseldorf. Italy) and manatined by other collaborators. In the next months a mirror of these applications will be made available on this server. Currently you can reach these web servers using the following links. Support Vector Machine based method to predict cancer-causing mutations (Beta version).

4

SNPs@BioFolD

http://snps.biofold.org/index.html

In this page are reported information about the projects related to the annotation of the impact of Single Nucleotide Variants (SNVs) on human health. Currently we have four available web tools located in our server:. Support Vector Machine based method to discriminate between neutral or disease-related single point protein mutations. Meta-predictor of disease causing variants that uses the output of PANTHER, PhD-SNP, SIFT and SNAP.

5

Meta-SNP - Meta-predictor of disease causing variants

http://snps.biofold.org/meta-snp

Meta-predictor of disease causing variants. One letter residue code. FA5 HUMAN nMFPGCPRLWVLVVLGTSWVGWGSQGTEAAQLRQFYVAAQGISWSYRPEPTNSSLNLSVTSFKKIVYREYEPYFKKEKPQSTISGLLGPTLYAEVGDIIKVHFKNKADKPLSIHPQGIRYSKLSEGASYLDHTFPAEKMDDAVAPGREYTYEWSISEDSGPTHDDPPCLTHIYYSHENLIEDFNSGLIGPLLICKKGTLTEGGTQKTFDKQIVLLFAVFDESKSWSQSSSLMYTVNGYVNGTMPDITVCAHDHISWHLLGMSSGPELFSIHFNGQVLEQNHHKVSAITLVSATSTTANMTVGPEGKWIISSLTPKHLQAGMQAYIDIKNCPKKTRNLKKITREQRRHMKRWEYFIAAEEVIWDYAPVIPANMDKKYRSQHLDNFSNQIGKHYKKVMYTQYEDESFTKHTVNPNMKEDGILGPIIRAQVRD...

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snps.biofold.org snps.biofold.org

SNPs@BioFolD

In this page are reported information about the projects related to the annotation of the impact of Single Nucleotide Variants (SNVs) on human health. Currently we have four available web tools located in our server:. Support Vector Machine based method to discriminate between neutral or disease-related single point protein mutations. Meta-predictor of disease causing variants that uses the output of PANTHER, PhD-SNP, SIFT and SNAP.

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