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: tom@gene-talk.de

Registergericht: Amtsgericht Berlin Charlottenburg
HRB 153711 B

Umsatzsteuer-Identifikationsnummer gemäß §27 a Umsatzsteuergesetz:
DE291652996

GeneTalk GmbH

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GeneTalk GmbH

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