Σάββατο 2 Νοεμβρίου 2019

Icon to click to save item to your GenomeWeb reading list. Breast Cancer Recurrence Risk Predicted by Immune-Related Germline Variants
Published on Nov 01, 2019
Icon to click to save item to your GenomeWeb reading list. Sysmex, Optim to Establish Digital Medicine Joint Venture
Published on Nov 01, 2019
Icon to click to save item to your GenomeWeb reading list. Castle Biosciences Stock Climbs in October, Clawing Back September Losses
Published on Nov 01, 2019
Icon to click to save item to your GenomeWeb reading list. In Brief This Week: Thermo Fisher Scientific, Curetis, OpGen, and More
Published on Nov 01, 2019
Icon to click to save item to your GenomeWeb reading list. Local Coverage Determinations Roundup: Transplant Genomics
Published on Nov 01, 2019
Icon to click to save item to your GenomeWeb reading list. People in the News: Matthew Sause, Scott Gottlieb, Don Kania, More
Published on Nov 01, 2019
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How to Avoid Contamination in Pipetting
This white paper from Sartorius addresses the three contamination types that originate from pipetting and discusses strategies for avoiding each.
Download it from GenomeWeb’s White Paper Channel.
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Live Webinar: Simultaneous Single-Cell DNA and Protein Sequencing in AML Samples
Linde Miles of Memorial Sloan Kettering Cancer Center will share data from the study demonstrating that simultaneous single-cell sequencing of DNA and protein can identify populations of stem/progenitor cells with distinct clonal/mutational and protein expression profiles.
Register Here
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Icon to click to save item to your GenomeWeb reading list. Inventor of Quanterix Tech Exploring Point-of-Care Simoa Device for Tuberculosis Detection
Published on Oct 24, 2019
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Icon to click to save item to your GenomeWeb reading list. MGI Tech Introduces Portable Sequencer, Single-Cell Prep Device; Launches New Sequencing Chemistry
Published on Oct 28, 2019
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Accelerated and AI-Based Genomic Workflows On-Premises and in the Cloud
Watch this on-demand webinar for an in-depth understanding of how GPUs can be used to accelerate industry-standard bioinformatics algorithms and deep learning technologies used in variant calling.
Download it from GenomeWeb’s Webinar library

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