Roche Launches NGS AVENIO Tumor Tissue Analysis Kits for Oncology Research
Ready-to-use kits determine genomic characteristics of solid tumours
Ready-to-use kits determine genomic characteristics of solid tumours
Exclusively licensed, rhabdovirus-free platform enables more productive bioprocessing
Scientists at The University of Manchester have discovered a genetic mutation in humans linked to a 17-fold increase in the amount of dangerous fungal spores in the lungs
ARESupa test aims at broad detection of microbial infections employing next-generation sequencing and artificial intelligence
Scientists at the National Center for Research on Human Genomics are at the forefront of groundbreaking research to develop new drugs for major diseases
SelectScience will be attending the AACC Annual Meeting in Chicago, USA, to interview leading scientists and report on the latest technologies
Learn about solutions for automated low-volume liquid handling for cost-effective NGS library preparation and single cell genomics
Read the latest on how 39 trillion bacteria in the gut regulate our health
The Oncomine TCR Beta-SR Assay for next-generation sequencing enables site-specific interrogation for T-cell receptor applications
New library preparation solution for targeted next-generation sequencing combines gene panel design customization with ultra-high sensitivity
Missed our fascinating NGS webinar? Catch up on demand and read the Q&A highlights below
From plastic-eating enzymes to nuclear disaster prevention, discover the top environmental stories of April 2018
Earlham Institute boosts national capability in genomics and single cell analysis with ultra-high throughput sequencing platform from Illumina
Five Prime Therapeutics and Personal Genome Diagnostics collaborate to develop new diagnostic assay for gastric and gastrointestinal cancers
Presentations on novel developments in CRISPR screening technologies and applications for the DriverMap™ targeted RNA expression profiling assay
New 2D tube with external thread from Micronic provides a simpler way to build your genomic libraries
Learn how to improve your NGS data reliability
Take an interactive tour of the Hyperion Imaging System and meet experts in imaging mass cytometry at the Fluidigm booth 3420
Non-invasive, cell-free pre-natal DNA testing to be performed on QIAGEN’s GeneReader NGS System