DESKGEN Series Libraries are designed and manufactured using the latest CRISPR gene editing techniques and artificial intelligence to deliver a tailored end-to-end solution London, UK – Desktop Genetics Ltd (“the Company”), a company revolutionizing the way biologists use CRISPR genome editing technology, has today announced the launch of its DESKGEN Series CRISPR Libraries to support gene […]

New CRISPR-based Transcriptional Activation and Interference (a/i) Libraries SANTA CLARA, Calif.   Agilent Technologies Inc. (NYSE: A) today announced the first expansion of the SureGuide pooled CRISPR libraries for functional genomics, offering pooled libraries for CRISPR activation and interference (CRISPR a/i). The announcement was made at the at the American Society for Human Genetics Conference (ASHG), […]

DESKGEN Series Libraries are designed and manufactured using the latest CRISPR gene editing techniques and artificial intelligence to deliver a tailored end-to-end solution London, UK – Desktop Genetics Ltd (“the Company”), a company revolutionizing the way biologists use CRISPR genome editing technology, has today announced the launch of its DESKGEN Series CRISPR Libraries to support gene […]

CLIA Sanger Sequencing also launched along with the announcement of a new PacBio® SMRT®Grant Program   South Plainfield, N.J. and Orlando, Fla. (ASHG17, Booth #323) — Leading global genomics service provider, GENEWIZ, launches CLIA Sanger sequencing and new NGS amplicon sequencing, at booth #323 during The American Society of Human Genomics (ASHG) Annual Meeting. ASHG is […]

Ness Ziona, Israel – NRGene, the worldwide leader in genomic assembly and analysis, has demonstrated its ability to discover, analyze, and track abnormalities within the human genome, across multiple subjects. As part of a proof of concept, NRGene’s GenoMAGICTM provided a complete analysis of a family’s genomic profile based on low (8X) coverage whole genome sequencing information. […]

ORLANDO, USA Strand NGS now supports large scale RNA- and small-RNA-Seq and Unique Molecular Identifiers (UMIs) for DNA-, RNA-, and small-RNA-Seq. Strand Life Sciences announced the latest version release of its bioinformatics flagship product, Strand NGS, at the Annual Meeting of the American Society of Human Genetics today. Two major themes in Strand NGS v3.1 […]

 SHANGHAI, CAMBRIDGE, Mass. and REYKJAVIK, Iceland — WuXi NextCODE, the contract genomics organization providing the global standard platform for genomic data, today announced the first open-access installation of Oxford Nanopore instruments in a CAP/CLIA lab in China – at WuXi NextCODE’s sequencing laboratory in Shanghai. “We are honored to introduce Oxford Nanopore’s pathbreaking capabilities to the breadth of the scientific and medical […]

– Linked-Reads will be used to advance precision health and personalized medicine – PLEASANTON, CA and SAINT GEORGE, UT –Intermountain Precision Genomics and 10x Genomics announced today, the addition of Chromium™ Genome Solution to the Translational Science Center (TSC). The center currently houses several of the latest high-throughput next-generation sequencing instruments for large-scale whole genome […]

SAN DIEGO– Illumina, Inc. (NASDAQ:ILMN) today announced the availability of the NovaSeq S4 flow cell, reagent kit and NovaSeq Xp workflow for its NovaSeq™ 6000 System. Flow cell innovation is key to unlocking the power and flexibility of the NovaSeq platform and the release of this new flow cell and workflow extends the capabilities of the platform […]

Coverage of the comprehensive, multi-biomarker test is now available to Regence BlueCross/BlueShield plan members in Oregon, Idaho, Utah and Washington CARLSBAD, Calif. — Thermo Fisher Scientific today announced its Oncomine Dx Target Test has received a positive coverage decision by Regence BlueCross/BlueShield. The declaration makes the next-generation sequencing (NGS)-based companion diagnostic for non-small cell lung cancer (NSCLC) available to […]