Roche has acquired Bina Technologies !!!
...mpany based in California. The biotech’s first product was the Bina Box, a platform for secondary genomic analysis, sequence alignment, and variant calling, but since 2012, it h...3376 days ago
Webinar on 'An integrated RNA and DNA approach to unravel genetic regulation in cancer'
...Mutations in the genome result in diverse transcriptional aberrations that can be missed in a stand-alone WES/WGS analysis. An integration of DNA variant analysis and RNA-Seq analysis...3333 days ago
Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017
Continuing our DNA-Seq webinar series, we'll present Strand NGS v3.0 best-practices: a workflow that identifies highly accurate variants from raw reads. Our best practices workfl...2533 days ago
Strand Life Sciences announces the release of Strand NGS v3.1 at ASHG 2017
...NA-Seq. UMI support in Strand NGS is end-to-end, spanning alignment to variant calling in DNA-Seq, and align...FFPE samples, UMI support in DNA-Seq enables the detection of somatic variants at low concentrations. In RN...2349 days ago
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598 Indian Genomes from 55 ethnic groups Sequenced
...disease management. This study has identified many genetic variants that are specific to Indian...lation groups that were previously not known. Some of these are common variants in the Indian groups, but wh...1567 days ago
The new corona variant has 23 mutations in all, which is unusually huge !
...ium) that analysed the genome data of the virus and identified the variant, the new variant has been spreading "rapidly"...nome sequences of SARS-CoV-2, of which 942 (32%) belong to the new variant. The Consortium intends...1192 days ago