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Webinar on Streamlining large scale analysis using the Strand NGS Pipeline Manager on 24 Feb 2016
...lly, we will show a brief glimpse of an elaborate pipeline that aligns reads, filters poor-quality matches, computes coverage metrics, identifies variants, checks for sample cross-cont...3001 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 workflo...2560 days ago
Strand Life Sciences announces the release of Strand NGS v3.1 at ASHG 2017
...fication of custom UMI protocols. “For liquid biopsies and low-grade FFPE samples, UMI support in DNA-Seq enables the detection of somatic variants at low concentrations. In RNA...2376 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 p...lation groups that were previously not known. Some of these are common variants in the Indian groups, but whe...1594 days ago