Search results for Next-Generation Sequencing

Next-generation sequencing has had a huge impact on molecular pathology lab

RNA sequencing and next generation sequencing expand cancer diagnostics by enabling multi gene analysis, improving mutation detection, and supporting targeted therapy decisions in...

Gel-free library preparation for next-generation RNA sequencing and small RNA quantification

RNA sequencing sensitivity improves with gel-free library preparation, reducing primer dimer artifacts and enhancing small RNA quantification from lower sample inputs...

CHOP researchers develop versatile and low-cost technology for targeted long-read RNA sequencing

Long-read RNA sequencing improves rare disease diagnosis by resolving transcript isoforms and variant effects, enabling more accurate interpretation of pathogenic splicing...

Integrated Sample Preparation System Standardizes and Streamlines Pre-Analytical Workflows

The Invivoscribe PrepQuant system is assay agnostic, generating highly concentrated genomic DNA and cell free DNA (cfDNA) yields for next-generation sequencing (NGS), qPCR, and dig...

Whole Genome & Transcriptome Sequencing: Costing Guide

In a groundbreaking development poised to revolutionize cancer diagnostics and treatment, a newly published study from Altbürger, Menzel, Beck, and colleagues explores the intricat...

Medgenome unveils india’s first study demonstrating the clinical impact of RNA-based NGS in sarcoma diagnosis

RNA sequencing improves sarcoma diagnosis by detecting gene fusions and refining classifications, enabling more accurate treatment decisions and better patient...

New FDA recommendations support next-generation sequencing-based safety evaluation of off-target editing for personalise...

FDA draft guidance highlights next-generation sequencing approaches for evaluating off-target effects and genomic integrity in genome editing therapies, supporting safer gene thera...

Building the Genome Grid

MGI Tech’s decade-long push helped turn sequencing into scalable, affordable global infrastructure. The post Building the Genome Grid appeared first on GEN - Genetic Engineering an...

Oxford Nanopore and Lonza Launch Direct RNA Sequencing Solution for GMP mRNA Quality Control

RNA sequencing combined with nanopore technology and machine learning may streamline GMP quality control testing for mRNA therapeutics within a single workflow...

Alida Biosciences launches EpiPlex® Tri-Mod™ service for simultaneous profiling of three key mRNA modifications

RNA sequencing now enables simultaneous detection of multiple RNA modifications alongside gene expression, providing deeper...

Advancing Fully Walkaway Automation in Genomics Workflows

EMBL GeneCore plans to expand facility capacity to develop new protocols and further validate and optimize existing workflows for applications such as low-input and metagenomics sa...

Caris Life Sciences announces launch of Caris ChromoSeq, the world’s first whole genome and whole transcriptome tumor pr...

Integrating RNA sequencing with whole genome analysis, Caris ChromoSeq delivers...

Programmable RNA detection enables multiplex virus identification

RNA sequencing advances support CRISPR-based detection methods that use kinetic signatures to identify multiple viruses and variants from RNA in a single, rapid diagnostic assay...

AGBT 2026 Recap: NGS Big Bets and Spatial’s Rising Momentum

For the genomics community February means the season of big announcements as the AGBT meeting—which has earned a reputation for breaking field-shaping news—takes place. The meeting...

FIRST-seq – a nanopore-based cDNA sequencing platform for RNA modification and structure profiling

RNA sequencing using nanopore technology enables detection of RNA modifications and structure at single-nucleotide resolution through reverse transcription error signatures...

Parse biosciences launches FFPE-compatible barcoding technology for whole transcriptome single cell analysis

Parse Biosciences enables RNA sequencing of FFPE samples at single cell resolution, unlocking archived tissues for whole transcriptome analysis and deeper insights into gene...

Children’s Hospital of Philadelphia researchers develop new RNA sequencing platform for diagnosing rare diseases

RNA sequencing using targeted long-read approaches enables detection of disease-causing variants by revealing how genetic changes disrupt full-length RNA molecules...

OHSU scientist uses advanced sequencing to develop treatments for oral infections

RNA sequencing with nanopore technology helps reveal how oral bacteria regulate genes, form biofilms, and may be targeted with more precise antimicrobial strategies...

Who Is Missing Out on Next-Generation Sequencing in Cancer?

RNA sequencing and genomic profiling adoption is rising across cancers, yet disparities in access and delayed testing continue to limit timely precision oncology treatment decision...

FUSILLI -long-read fusion detection

RNA sequencing with FUSILLI improves detection of leukemia fusion oncogenes, supporting more accurate molecular diagnosis and subtyping in pediatric B-cell acute lymphoblastic leuk...

The State of Multiomics & NGS

In our April 29 virtual summit GEN invites you to watch a superb line-up of presenters covering key topics in the world of multiomics, spatial biology, and NGS. The post The State...

Non-destructive transcriptomics via vesicular export

RNA sequencing with NTVE enables repeated monitoring of gene expression in living cells, supporting time-course analysis of differentiation, perturbation responses, and cellular dy...

Molecular Eyes on the Bile Duct: Next-Generation Sequencing Earns Its Place in Biliary Stricture Evaluation

Genomic testing for advanced cancer improving but still lags

Nearly half of people diagnosed with advanced cancer over a recent 5-year period did not undergo next-generation sequencing, according to results of a retrospective cohort study.Ra...