GeneTalk

30/05/2016

A lesson on how to filter NGS data from targeted RNA sequencing.

http://blog.gene-talk.de/?p=647

Variants in noncoding regions are always difficult to interpret on genomic level . In a recently published article in Human Mutation entitled

05/11/2014

blog.gene-talk.de/?p=545

Power does not consist in striking with force but in striking with frequency! We adapted slightly Balzac’s catechism so that it can now be applied to sequence variants. We updated GeneTalk’s frequency filter with the genotype data of more than 65,000 exomes from the Exome Aggregation Consortium. Tha…

18/06/2014

New case solved with GeneTalk: http://www.ncbi.nlm.nih.gov/pubmed/24916641
Congratulations Mateusz!

PubMed comprises more than 23 million citations for biomedical literature from MEDLINE, life science journals, and online books. Citations may include links to full-text content from PubMed Central and publisher web sites.

27/05/2014

GeneTalk company portrait made by Uni Potsdam: http://vimeo.com/95735504

GeneTalk ist eine webbasierte Software und ein Expertennetzwerk zur Auswertung und Interpretation genetischer Daten in der Diagnostik von Erbkrankheiten. GeneTalk…

19/12/2013

An interesting Article about GeneTalk and how researchers found new disease causing genes via collaborations promoted by GeneTalk in GEN: http://www.genengnews.com/insight-and-intelligence/gene-research-follows-the-crowd/77899987/

GeneTalk links rare-disease geneticists, stokes collaborations.

29/10/2013

GeneTalk supports the Personal Exome Project for identifying rare genomic disorders. Please help with the fundraising on https://www.microryza.com/projects/personal-exome-project
And please share this link.

Personal Exome Project

21/08/2013

Verena Heinrich, Tom Kamphans, Jens Stange, Dmitri Parkhomchuk, Thorsten Dickhaus, Jochen Hecht, Peter N Robinson and Peter M Krawitz

21/08/2013

New publication out by V. Heinrich:
Estimating Exome Genotyping Accuracy by Comparing to Data from Large Scale Sequencing Projects

read more in GeneTalk Blog:

http://blog.gene-talk.de/?p=434

A new paper was published in Genome Medicine about how genotyping accuracy is estimated by comparing variant data with data from large scale sequencing projects such as the 1000 Genomes Project.

08/08/2013

GeneTalk will be present at the in Boston. Meet us at booth no. 1054

07/08/2013

New publication out: Filtering for Compound Heterozygous Sequence Variants in Non-Consanguineous Pedigrees

http://blog.gene-talk.de/?p=426

Kamphans et al. published an artile about on which basis the filter for compound heterozygous sequece variants works in GeneTalk.

28/06/2013

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