allelefrequencycommunity.org

Allele Frequency Community

Imagine Human genome interpretation minus the false positives. The Allele Frequency Community is a freely accessible opt-in community resource designed to facilitate sharing of anonymized, pooled allele frequency statistics among laboratories for the benefit of patients and biomedical research. Joining the community is free. Once you join, your NGS samples can be richly annotated with allele frequency information from the entire Community. Non-personally identifiable statistics from community...

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Allele Frequency Community | allelefrequencycommunity.org Reviews

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Imagine Human genome interpretation minus the false positives. The Allele Frequency Community is a freely accessible opt-in community resource designed to facilitate sharing of anonymized, pooled allele frequency statistics among laboratories for the benefit of patients and biomedical research. Joining the community is free. Once you join, your NGS samples can be richly annotated with allele frequency information from the entire Community. Non-personally identifiable statistics from community...

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Allele Frequency Community | allelefrequencycommunity.org Reviews

https://allelefrequencycommunity.org

Imagine Human genome interpretation minus the false positives. The Allele Frequency Community is a freely accessible opt-in community resource designed to facilitate sharing of anonymized, pooled allele frequency statistics among laboratories for the benefit of patients and biomedical research. Joining the community is free. Once you join, your NGS samples can be richly annotated with allele frequency information from the entire Community. Non-personally identifiable statistics from community...

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allelefrequencycommunity.org

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FAQs

http://www.allelefrequencycommunity.org/faqs

Q: Does the AFC dataset contain healthy (normal) samples only? A: No, it does contain individuals affected with phenotypes as well as individuals who are free of known genetic disease. In cases where family structures were provided, parental/founder genomes were used, but not the children to reduce family bias. Q: What are we filtering against? Ie: what are the specs to which a sample must meet to be entered into the AFC? How do we capture this? A: Self-identified ethnic background was provided by a subs...

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Insights through Diversity

http://www.allelefrequencycommunity.org/insights-through-diversity

A key challenge in genome interpretation and precision medicine is the lack of an extensive, high quality, ethnically-diverse collection of human genomes as a reference set. A prospective disease-causing variant that appears to be rare based on publicly available sequence may in fact be a polymorphism in an ethnic population under-represented in public databases. Resources such as the Exome Variant Server. Project, and the Exome Aggregation Consortium. And QIAGEN Clinical Insight.

3

Co-founders

http://www.allelefrequencycommunity.org/co-founders

Stan Letovsky & Thomas Kaminski. Associate VP for clinical bioinformatics & General manager, Enlighten Health Genomics (division of LabCorp). Founding Member Snapshot: LabCorp. Thomas Kaminski, general manager of Enlighten Health Genomics, and Stan Letovsky, associate vice president for clinical bioinformatics at LabCorp. Kaminski notes the importance in making sequencing data more meaningful for translational work. “At the end of the day, hopefully this will continue to increase the diagnostic...Letovsk...

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Our website uses cookies. By using our website and agreeing to this policy, you consent to our use of cookies. Learn more. Center for Genomic Medicine. Institute for Clinical Genetics. Module and plugin overview. CLC Genome Finishing Module. CLC Microbial Genomics Module. Interpretation and Content Databases. QCI Interpret – somatic. QCI Interpret – hereditary. Biomedical Genomics Server Solution. CLC Server Command Line Tools. Module and plugin downloads. It’s in our DNA. CLC bio is the leading bioinfor...

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Our website uses cookies. By using our website and agreeing to this policy, you consent to our use of cookies. Learn more. Center for Genomic Medicine. Module and plugin overview. CLC Genome Finishing Module. CLC Microbial Genomics Module. Interpretation and Content Databases. QCI Interpret – somatic. QCI Interpret – hereditary. Biomedical Genomics Server Solution. CLC Server Command Line Tools. Module and plugin downloads. Solve the complexity of cancer research. See the whole picture. Get results faste...

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Our website uses cookies. By using our website and agreeing to this policy, you consent to our use of cookies. Learn more. Center for Genomic Medicine. Module and plugin overview. CLC Genome Finishing Module. CLC Microbial Genomics Module. Interpretation and Content Databases. QCI Interpret – somatic. QCI Interpret – hereditary. Biomedical Genomics Server Solution. CLC Server Command Line Tools. Module and plugin downloads. Monday, August 10, 2015. Webinar: Learn about the key capabilities of QCI.

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Our website uses cookies. By using our website and agreeing to this policy, you consent to our use of cookies. Learn more. High volume sequencing solution. Center for Genomic Medicine. CLC Genome Finishing Module. CLC Microbial Genomics Module. Interpretation and Content Databases. QCI Interpret – somatic. QCI Interpret – hereditary. Biomedical Genomics Server Solution. Are you ready to uncover the signals that lead to breakthrough discoveries in your human disease research? Specialized functionalities s...

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http://www.clc-bio.dk/products/clc-genomics-workbench

Our website uses cookies. By using our website and agreeing to this policy, you consent to our use of cookies. Learn more. High volume sequencing solution. Center for Genomic Medicine. CLC Genome Finishing Module. CLC Microbial Genomics Module. Interpretation and Content Databases. QCI Interpret – somatic. QCI Interpret – hereditary. Biomedical Genomics Server Solution. Check out the features. CLC Genomics Workbench is developed to support a wide range of NGS bioinformatics applications. The workbenc...

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allelefrequencycommunity.org

Allele Frequency Community

Imagine Human genome interpretation minus the false positives. The Allele Frequency Community is a freely accessible opt-in community resource designed to facilitate sharing of anonymized, pooled allele frequency statistics among laboratories for the benefit of patients and biomedical research. Joining the community is free. Once you join, your NGS samples can be richly annotated with allele frequency information from the entire Community. Non-personally identifiable statistics from community...

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