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rna-seqblog.com /1 month ago

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...

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genengnews.com /1 month ago

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...

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genengnews.com /1 month ago

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...

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rna-seqblog.com /1 month ago

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...

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genengnews.com /1 month ago

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...

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rna-seqblog.com /1 month ago

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FDA draft guidance highlights next-generation sequencing approaches for evaluating off-target effects and genomic integrity in genome editing therapies, supporting safer gene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

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rna-seqblog.com /1 month ago

Alida Biosciences launches EpiPlexÂ® Tri-Modâ„¢ service for simultaneous profiling of three key mRNA modifications

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

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rna-seqblog.com /1 week ago

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...

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rna-seqblog.com /2 weeks ago

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...

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bioengineer.org /1 month ago

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...

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rna-seqblog.com /1 month ago

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...

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genengnews.com /1 month ago

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...

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food-safety.com /1 month ago

USDA-FSIS Updates WGS Laboratory Method

The updated Microbiology Laboratory Guidebook chapter on whole genome sequencing (WGS) of bacterial isolates now includes protocols for using both the Illumina MiSeq and MiSeq i100...

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bioengineer.org /3 weeks ago

Cell-free DNA reveals tumor-linked nucleosomal patterns

In a revolutionary breakthrough poised to redefine cancer diagnostics, researchers have unveiled a cutting-edge technique that meticulously dissects the size of cell-free DNA fragm...

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genengnews.com /1 month ago

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...

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rna-seqblog.com /1 month ago

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...

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nanowerk.com /1 month ago

New gene editing method inserts large DNA segments to rewrite genome chapters

A new prime assembly technique inserts DNA segments up to 11,000 base pairs into the genome, enabling correction of thousands of mutations at once.

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rna-seqblog.com /1 month ago

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...

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bioengineer.org /1 month ago

Breakthrough in Metagenomic Software Accelerates Microbial Diversity Research

In the evolving realm of metagenomics, the ability to reconstruct individual microbial genomes from complex environmental and clinical samples stands as a transformative scientific...

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healio.com /1 month ago

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...

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bioengineer.org /3 weeks ago

New TGen Clinical Test Streamlines Multiple Myeloma Analysis, Delivering Comprehensive Results in Just 3 Days

The Translational Genomics Research Institute (TGen), a proud division of City of Hope, has unveiled a groundbreaking advancement in the field of precision oncology with the launch...

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genengnews.com /2 weeks ago

Genewiz Launches Gene Synthesis 2.0

Gene Synthesis 2.0 introduces upgraded codon optimization capability combining heuristic approaches with machine learning models trained on a high expression dataset that can impro...

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rna-seqblog.com /3 weeks ago

AI-powered, next-generation sequencing blood-based assay evaluated for detection of post-HCT relapse in AML and MDS

RNA sequencing and AI-powered blood monitoring may detect relapse earlier after hematopoietic cell transplantation, improving risk prediction in AML and myelodysplastic syndrome pa...

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nanowerk.com /2 weeks ago

DNA barcoding platform finds gold nanoparticles for precision cancer therapy

A new high-throughput platform screens dozens of nanoparticle designs in living systems to identify those that reach tumor mitochondria, enabling more precise and effective cancer...

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