Results for "webinar"
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Webinar: Wednesday 21 August 2013 at Noon EDT
This webinar will describe the use of combinatorial pooling to reconstruct gene sequences within BACs. Recent work in barley has shown that this level of sequence knowledge is sufficient to support critical end-point objectives such as map-based cloning and marker-assisted breeding. http://www.e...Tags: Webinar, Selective Sequencing, Gene, BAC
3904 days ago
- This webinar will describe an R based approach to considerably speed GWAS computation time on a notebook book computer. More http://www.extension.org/pages/68354/upcoming-webinar:-fast-semi-parallel-linear-and-logistic-regression-for-genome-wide-association-studi#.UjCL9azyPqV Register @ https:/...
Tags: R, Webinar, GWAS
3874 days ago
- In less than two weeks, NCBI will offer a webinar entitled "Introducing 3 NCBI Resources to Navigate Testing for Disease Linked Variants: MedGen, GTR and ClinVar". This webinar will delve into the lifecycle of genetic testing and teach attendees how to navigate the NIH Genetic Testing Registry, C...
Tags: Bioinformatics, Computational Biology, Webinar, Protein, GTR, Disease
3604 days ago
Live Webinar on RNA-Seq Data Analysis on 9 Nov 2016
Live Webinar on RNA-Seq Data Analysis Abstract: Strand NGS supports an extensive workflow for the analysis and visualization of RNA-Seq data. The workflow includes Transcriptome / Genome alignment, Differential expression analysis with Statistical approach and Splicing events detection. Strand N...Tags: Strand NGS, Webinar, RNA-Seq, NGS, Sequencing
2740 days ago
- Free Live Webinar on Leukocyte immunobiology helps us predict post-operative risk using pre-operative markers on 9 Aug, 8 am PST Speaker: Mario Deng MD FACC FESCProfessor of MedicineAdvanced Heart Failure/MechanicalSupport/Heart TransplantDavid Geffen School of Medicine at UCLARonald ...
Tags: Webinar, Transcriptome analysis, flow cytometry, Strand NGS, Prof Mario Deng, UCLA, Strand Life Sciences
2468 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 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
2556 days ago
- Live webinar on Unravelling complex mutational events in clinical cases using the power of Next generation sequencing data analysis by Dr Satish Sankaran on 31 Jan 2018 at 9am CET and 8am PST Speaker: Dr. Satish Sankaran, Vice President and Lab Director - Clinical Operations & Clin...
Tags: strand ngs, webinar, clinical cases
2294 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
2249 days ago
- A disease is considered to be ‘rare’ when it affects one in about 2000 individuals in the population. This, individually are although rare, collectively, the incidence could be very high causing a significant socio-economic burden. Arriving at a confirmatory diagnosis is a major chall...
Tags: strand ngs, webinar, rare disease, clinical diagnosis, dna-seq
2224 days ago
