GeneTalk GmbH

medical devices

About

Analyze human genetic sequence variants GeneTalk is what physicians and scientists working on human next-generation sequencing (NGS) data sets have dreamed of: You want to analyze a human genetic variants in an NGS data set in the standard variant call format (VCF) for disease causing variants? GeneTalk enables you to manage your NGS variant data effectively: Filter GeneTalk assists you in filtering your data for rare genetic variants by providing a powerful filter that is adaptable for different inheritance models and frequency cutoffs Annotate GeneTalk annotates your coding as well as your non-coding variants. Investigate GeneTalk guides you to the latest scientific publications related to your variants of interest. Communicate And best of all: GeneTalk is interactive! As soon as you filtered your data set down to a few hot candidates it refers you to an expert scientist who is interested in exactly your mutation and who might give you valuable advice on prioritizing your disease candidates. Impressum (Angaben gemäß § 5 TMG) GeneTalk GmbH Retzbacher Weg 83 13189 Berlin Vertreten durch: Dr. Peter Krawitz Dr. Tom Kamphans Kontakt: Telefon: 017649942424 E-Mail: [email protected] Registergericht: Amtsgericht Berlin Charlottenburg HRB 153711 B Umsatzsteuer-Identifikationsnummer gemäß §27 a Umsatzsteuergesetz: DE291652996

Technologies

Ruby On Rails Nginx YouTube Google Font API Mobile Friendly Phusion Passenger Bootstrap Framework Remote

Keywords

medical equipment manufacturing biotechnology monogenic disorders expert curated gene panels polygenic risk modeling medical image analysis genetic data integration ngs data filtering services rare genetic disorder diagnosis variant prioritization genetics genetic analysis platform ngs data analysis next-generation phenotyping human sequence variants research and development in the physical engineering and life sciences genome-wide risk modeling genome-wide prs personalized medicine tools genetic mutation discussion variant discussion platform clinical variant interpretation face2gene integration pedia phenotypic similarity scoring genetic research tools clinical genetics risk stratification

Location

83 Retzbacher Weg, Berlin, Berlin, Germany, 13189

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