Leverages Advanced Magnetic Bead-Based Technology to Support Next Gen Sequencing, Genotyping, PCR and MLPA in Human Samples   WHAT:              PerkinElmer, Inc., a global leader committed to innovating for a healthier world, today announced the launch of its chemagic™ Prime™ instrument, a new streamlined, walk-away sample processing solution which offers automated nucleic acid isolation and assay setup by combining […]

– Customer data and updated pricing will be presented at the 67th Annual Meeting of the American Society of Human Genetics (ASHG) held in Orlando, FL – PLEASANTON, CA.—10x Genomics, a company focused on enabling the mastery of biology by accelerating genomic discovery, today announced more affordable pricing for their Chromium™ Genome, Exome and de novo Assembly […]

Ability to apply the highly sensitive and affordable technology for non-invasive tumor-specific DNA detection brings the holy grail of early cancer detection one step closer. SAN DIEGO Nanomedical Diagnostics, a life science company pioneering the use of label-free graphene biosensors in the healthcare industry, announces the grant of U.S. Patent No. 9,765,395 by the United […]

Oxford Nanopore is developing target enrichment processes for the nanopore sequencing platform, based on the CRISPR/Cas9 system. When coupled with real-time nanopore DNA analysis, these techniques are designed to help users target and resolve specific biological questions more quickly and efficiently than possible with whole genome sequencing. The first participants are preparing to use the […]

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 […]