Integrating > 120 key data sources, the GeneCards® Suite Knowledgebase empowers your Next Generation Sequencing analysis by highlighting associations between genes and phenotypes, providing supporting evidence for immediate evaluation and automatically generating case reports.
TGex can be deployed on the cloud or on premises, providing you with the freedom to choose how and where you work.
When installed within your firewall, integrate it with your commercial databases and internal and external data sources. Create your own in-house proprietary database based on your own sequencing data.
TGex makes it easy for you to scale up your NGS core capabilities.Read more
Having analyzed hundreds of cancer cases using NGS, I've found TGex to be a great tool for evaluating variants and analyzing multiple samples like tumor-germline pairs or familial cases. TGex clearly significantly boosts the access of relevant information for the translation of the genomic information into clinical decision making. Furthermore, the user interface is comfortable, highly flexible and interactive, and reduces the time invested in each analysis. Altogether, I highly recommend TGex as a platform for analysis of cancer cases, and as a tool to preparing a report of genomic information to be provided to clinical care professionals.
I have had the pleasure of working with VarElect and TGex... which have an uncanny ability in discovering the right “culpable” variant in complex cases studied with whole exome sequence (WES)... both these programs have been extremely useful in our WES analyses. They are simple to use and yet most efficient. Thus, I recommend them very strongly.
TGex is an easy-to-use system for managing our genetic tests. It makes it easy to identify variants of relevance through its integration with various sources of evidence, and its ability to customize reports allows us to present our results to clients in the most useful manner. We strongly recommend it for labs that provide genetic information to clinical care professionals.
Dvir Dahary, Yaron Golan, Yaron Mazor, Ofer Zelig, Ruth Barshir, Michal Twik, Tsippi Iny Stein, Guy Rosner, Revital Kariv, Fei Chen, Qiang Zhang, Yiping Shen, Marilyn Safran, Doron Lancet & Simon Fishilevich
Genome analysis and knowledge-driven variant interpretation with TGex,
BMC Med Genomics 12, 200 (2019) [PDF]