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Breaking News

Celsius Therapeutics, Janssen Biotech Form Biomarker Discovery Alliance Published on Jul 09, 2019

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Japan, China Launch Basket, Umbrella Trials to Expand Precision Oncology Treatment Access Published on Jul 03, 2019

Vanderbilt Sample Prep Method May Enable Whole-Blood Malaria Drug Resistance Test at Point of Care Published on Jul 02, 2019

Human Glycome Project Forges Ahead With Support From New England Biolabs, Genos, Waters Published on Jul 02, 2019

MMRF to Bolster Recently Launched Clinical, Genomic Patient Data Registry With Immune Profiles Published on Jul 01, 2019

Proteomics for Precision Medicine: New Workflows to Support Translational Research  This webinar will address new translational workflows to support proteomic profiling for biomarker discovery through precision medicine. Register Here

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Invitae Launches Free Genetic Testing Programs With Spark Therapeutics, X4 Pharmaceuticals Published on Jun 12, 2019  Element Biosciences Raises $15M in Series A Financing Published on Jun 18, 2019

Cut Time from CRISPR Workflows  In this whitepaper from NanoCellect, learn how the WOLF Cell Sorter saves time and resources in CRISPR studies by selecting highly sensitive and fragile cells that would be difficult or impossible to select with traditional technologies. Download it from GenomeWeb’s White Paper Channel.

Job listings

Molecular Diagnostics - Development and NGS Data Scientist Company: SUNY Upstate Medical University Location: Syracuse NY Apply now

Postdoctoral Associate Company: New York University Location: New York NY Apply now

Principal Scientist, Cambridge, MA Company: Sanofi Location: Cambridge MA Apply now

Sr. Associate Scientist, Immunophenotyping and NGS - Cambridge, MA Company: Sanofi Location: Cambridge MA Apply now

New Technology to Generate Comprehensive ctDNA Reference Materials for Next Generation Sequencing  This poster video from SeraCare shows how the company developed a custom VariantFlex library, making highly customizable materials for any ctDNA profiling workflow possible. Download it from GenomeWeb’s Webinar library