Data-Processing Tool Could Support Early-Stage Cancer Detection
Researchers developed a platform for integrating DNA and RNA data from single-cell sequencing with improved speed and precision.
Researchers developed a platform for integrating DNA and RNA data from single-cell sequencing with improved speed and precision.
The Jackson Lab for Genomic Medicine is offering a clinical whole genome sequencing test to improve the diagnostic power of sequencing.
The study's multi-cancer early detection data show Exai's RNA- and AI-based platform can detect multiple cancer types at the earliest stages using a single, standard blood sample.
Tecan and Element Biosciences are collaborating to offer an improved benchtop NGS workflow with MagicPrep NGS and the AVITI System.
Read MoreTecan has partnered with Singular Genomics to use its turnkey MagicPrep NGS system to help create sequencing-ready libraries.
Read MoreBio-Rad Labs is showcasing compatibility of its SEQuoia RNA library preparation kits with new innovative sequencers.
Read MoreThermo Fisher Scientific launched its Applied Biosystems TaqPath Seq HIV-1 Genotyping Kit, an assay that examines positive samples of HIV.
Read MoreThe liquid biopsy ctDx FIRST test is FDA approved as a companion diagnostic for advanced non-small cell lung cancer (NSCLC) patients.
Read MoreQIAGEN Digital Insights unveiled their enhanced genomics workbench that removes the data-analysis bottleneck of next-generation sequencing.
Read MoreResearchers developed a new tool that can more accurately discover and quantify RNA molecules from error-prone long-read RNA sequencing data.
Read MoreResearchers have made an advancement in genetic testing that allows for more accurate prediction of individual’s increased cancer risk.
Read MoreThe SeCore CDx HLA Sequencing System was granted De Novo Classification as a companion diagnostic with Immunocore’s T cell receptor therapy.
Read MoreBroad-based genetic testing gives clinicians better insights into chronic kidney disease, improving the odds of a good transplant outcome.
Read MoreThermo Fisher Scientific has updated its Applied Biosystems 3500 and 3500xL DX genetic analyzers to comply with IVDR regulations.
Read MoreResearchers have uncovered new genes associated with autism spectrum disorder (ASD) in the largest autism whole genome sequencing to date.
Read MoreTailoring the analysis of whole genome sequencing to individual patients could double the diagnostic rates of rare diseases.
Read MorePrecision for Medicine detailed its NGS initiative which aims to improve the accuracy and speed of identifying cancer mutations in tumors.
Read MoreThe PancreaSeq molecular test accurately classifies pancreatic cysts as potentially cancerous or benign, a large, multi-center study found.
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