Found 88 presentations matching your search
Snippy - rapid haploid variant calling and core SNP alignments.
Using Snippy to call variants in bacterial short read datasets via alignment to reference, and then ...
In this article, I’ll explore the probabilities of two different labs achieving a 100% match in va...
Overview of why pangenome references can make a difference to patients and drug developers, framed a...
Recent webcasts have been focused on our latest features in Pharmacogenomics and the IVDR announceme...
CALGARY, Alberta, Aug. 20, 2024 (GLOBE NEWSWIRE) -- BioAro, a leading precision health and genomics ...
Earlier this year, we released VarSeq 2.3.0 which brought massive updates to our VSClinical AMP inte...
Since our release of the PGx capabilities in VarSeq, we’ve had a few months to gather some insight...
Learn how VSWarehouse transforms per-sample analyses into scalable institutional knowledge—streaml...
Multiple gene mutation can be done
The value of complex variant analysis has become increasingly apparent as long-read sequencing techn...
Clinical Genetic testing requires a complex analysis using the totality of our knowledge about the c...
A fantastic document with over all information about BFiS.
The advent of long read sequencing has opened the door to a more complete NGS pipeline. The current ...
• “Re- Launching of failed product” and the product name was “Nokia N Gage”.
A transition period regarding in vitro medical device (IVD) regulation in the European Union (EU) is...
this document provide explanation of the introduction of human and microorganism genome analysis
A complete overview on Royal Enfield Motorcycle corporation.
GenomeBrowse, a free visualization tool for all types of sequence data, was introduced in 2012 to br...
Introduction to mobile computing
Discover the Sitecore Personalize SDK, a new SDK to create assets in Sitecore Personalize programmat...
Clinical laboratories and genomic research centers are increasingly seeking flexible deployment opti...
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