Pairing the multi-discipline Clinisys Laboratory Solution with SciNote’s intuitive SaaS ELN platform, provides capabilities for users to streamline workflows, accelerate research, and unlock data’s true potential in an innovative, connected solution. Clinisys, a global provider of intelligent laboratory information management solutions, announces a strategic partnership with SciNote, a global market leader that provides an Electronic [...]

SAN DIEGO -- Armonica Technologies, Inc., a pioneer in sample-prep free direct optical DNA sequencing, today announced the appointment of life science leader Todd Dickinson to the Board of Directors. Armonica Technologies is a MedTech company focused on developing its advanced long-read sequencing platform for precision medicine applications. The company utilizes nanochannels to transport individual nucleic acid molecules through [...]

Curio Bioscience licenses a novel method from the Broad Institute of MIT and Harvard to fuel the next generation of discovery research PALO ALTO, Calif. – Curio Bioscience today announced the commercialization of the world’s first technology that spatially contextualizes single-cell sequencing data, leveraging a breakthrough invention called Slide-tags developed by the Broad Institute of MIT [...]

Global leader in Biopharma R&D chooses the Genedata Biopharma Platform to accelerate discovery timelines for protein-based modalities Basel, Switzerland — Genedata, the leading provider of enterprise software solutions for biopharmaceutical R&D, announced today that Daiichi Sankyo, a global pharmaceutical company with corporate origins in Japan, has adopted Genedata Biologics® to automate its discovery workflows. The [...]

HiFi Long-Read Sequencing Panel Supports Comprehensive Analysis of 20 Genes Associated With Neurological Disease MENLO PARK, Calif. -- PacBio (NASDAQ: PACB), a leading developer of high-quality, highly accurate sequencing solutions, today announced the PureTarget repeat expansion panel, a new solution designed to enable the comprehensive analysis of 20 genes associated with serious neurological disorders, including challenging-to-sequence genes [...]

Fostering Relationships with the NATO Support and Procurement Agency and the DrugDetect EU project, 908 Devices’ MX908 Deployed Across Europe for Trace Chemical Detection and Identification BOSTON -- 908 Devices Inc. (Nasdaq: MASS), a pioneer of purpose-built handheld and desktop devices for chemical and biochemical analysis, announces the latest in international adoption of the MX908 for [...]

TOKYO -- Rigaku, a global solution partner in X-ray-analysis proudly announces the opening of its new Rigaku Taiwan Branch ("RCTW"). This expansion marks a significant milestone in Rigaku's longstanding commitment to advancing the semiconductor electronics, life and material science ecosystem, particularly in Taiwan, a critical region for technological advancement. Technical supports offered by RCTW underscores [...]

Antibody-drug conjugates are gaining traction as an alternative or complementary therapy for different types of cancers Contest opened March 11, 2024; five winners will spend three weeks in Uppsala, Sweden testing their innovations Biotech firms and academic researchers interested in accessing a live bioprocess run for their technical and digital innovation projects are encouraged to [...]

Opentrons for Education transforms the classroom experience by introducing lab automation into educational settings By empowering educators with user-friendly automation tools, this program ensures students gain invaluable skills that are crucial for their future careers BROOKLYN, N.Y. -- Opentrons Labworks, Inc., a leader in lab automation and makers of accessible lab robotics, today announced the [...]

– An Invitae-developed innovative approach to help reduce variants of uncertain significance – SAN FRANCISCO -- Invitae (OTC: NVTA), a leading medical genetics company, today announced the launch of an update to Invitae Generation™ with Clinical Variant Modeling, a novel machine learning approach designed to aid clinical interpretation of genetic testing results and increase the rate of definitive [...]