fathmm - Home

Predict the Functional Consequences of Coding and Non-Coding Variants

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This site fathmm.biocompute.org.uk currently has an average traffic classification of zero (the smaller the better). We have probed zero pages within the domain fathmm.biocompute.org.uk and found thirty-four websites associating themselves with fathmm.biocompute.org.uk.
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Chloé-Agathe Azencott

Machine learning for therapeutic research. We at the Paris Women in Machine Learning and Data Science Meet-Up. Are very happy to open our slack channel.

Just an ordinary blog by an ordinary bloke by A. Mesut Erzurumluoğlu

Just an ordinary blog by an ordinary bloke.

Mooney Lab - MutDB Home

MutDB - A database for assessing the impact of genetic variants. Browse by First Letter of Gene Symbols. An identifier can be gene symbol, protein or transcript RefSeq, dbSNP, SwissVar, or COSMOC identifiers.

COSMIC Catalogue of Somatic Mutations in Cancer - Home Page

High quality curation by expert postdoctoral scientists. Additional tools to explore COSMIC. How do we annotate genomes? Genomic Landscape of Cancer. Displays all mutation information across all cancers and has been enhanced in v73 to include ENCODE regulatory features and all available SNPs. For more details, please see the datasheet.

COSMIC Catalogue of Somatic Mutations in Cancer - Home Page

High quality curation by expert postdoctoral scientists. Additional tools to explore COSMIC. How do we annotate genomes? Genomic Landscape of Cancer. Displays all mutation information across all cancers and has been enhanced in v73 to include ENCODE regulatory features and all available SNPs. For more details, please see the datasheet.

RVS the Reference Variant Store

Entry points are searches by specific coordinate, dbSNP, or gene; or a comparison of cohorts based on populations in RVS. The first four queries are also wrapped in our REST API. Enter one or more genes and, optionally, genetic variants to search RVS. Enter a phenotype or disease name, and optionally a gene to search. Some pages require an HTML5-capable w.

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FATHMM.BIOCOMPUTE.ORG.UK HOST

We observed that a single root page on fathmm.biocompute.org.uk took six thousand eight hundred and sixty milliseconds to download. Our crawlers could not find a SSL certificate, so our web crawlers consider this site not secure.
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137.222.108.103

SERVER OPERATING SYSTEM

I detected that this website is utilizing the Apache operating system.

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fathmm - Home

DESCRIPTION

Predict the Functional Consequences of Coding and Non-Coding Variants

CONTENT

This site fathmm.biocompute.org.uk states the following, "Functional Analysis through Hidden Markov Models v2." Our analyzers noticed that the webpage also stated " A high-throughput web-server capable of predicting the functional consequences of both coding variants, i." The Website also stated " non-synonymous single nucleotide variants nsSNVs, and non-coding variants. Use this option to return predictions capable of discriminating between disease-causing mutations and neutral polymorphisms. Use this option to return predictions capable of distinguishing between cancer-promotingdriver mutations and other germline polymorphisms." The website's header had Missense Mutation as the most important keyword. It was followed by Functional Effects, Inherited Disease Mutation, and Cancer Associated Mutation which isn't as ranked as highly as Missense Mutation. The next words the site used was Amino Acid Substitutions. Hidden Markov Models was also included but might not be seen by search parsers.

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The past cannot be changed, the future is still in your power. Friday, January 21, 2011. Friday, January 14, 2011. So i have a very kind teacher who knew me well, she helped me alot! Would like to Thank all Teachers, Family and friends for all the s.

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