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 workflow is twice as fast as its GATK counterpart, and results in precision/recall rates of up to 99%/98% on whole exome...Tags: webinar, strand ngs, variant calling, dna-seq, bwa-gatk
2555 days ago
Tags: strand ngs, webinar, clinical cases
2293 days ago
Webinar on RNA-Seq Data Analysis on 28 Feb 2018
Strand NGS is a biologist friendly NGS analysis tool that allows biologists to analyze their data using a very intuitive workflow for the analysis and visualization of RNA-Seq data. This webinar will give an overview of the workflow which includes Transcriptome/ Genome alignment, Differential exp...Tags: rna-seq, webinar, strand ngs, ngs data analysis
2248 days ago
Tags: strand ngs, webinar, rare disease, clinical diagnosis, dna-seq
2223 days ago
Tags: strand NGS, hereditary cancer, ovarian breast cancer, retinoblastoma
2788 days ago