Social Media Ideas for Illumina Sequencing

Illumina Announces MRD Kit Ahead of ASCO Meeting

Ahead of ASCO 2026, Illumina unveiled an early-access MRD research kit using whole-genome sequencing and DRAGEN analysis, enabling highly sensitive cancer monitoring workflows on N...

Roche launches Axelios 1, its eagerly awaited gene sequencing rival to Illumina

Roche may have failed to buy out Illumina back in 2012, but now it’s trying to take up some of the gene sequencing specialist’s market share with its own next-gen platform.

New England Biolabs® launches the NEBNext® Companion Module for Oxford Nanopore Technologies® Direct RNA Sequencing

New England Biolabs introduces a new RNA sequencing companion module that simplifies direct native RNA sequencing with Oxford Nanopore for transcriptomics and RNA...

Analyst Report: Illumina Inc

EclipseBio expands eCOMPASSâ„¢ platform with eSENSE Breakâ„¢ to map RNA fragmentation at nucleotide resolution

Eclipse Bioinnovations uses RNA sequencing in eSENSE Breakâ„¢ to map RNA fragmentation at single-nucleotide resolution, helping developers understand RNA stability and structural v...

Amaranth – enhanced single-cell transcript assembly via discriminative modelling of UMI reads and internal reads

Amaranth improves transcript reconstruction from RNA sequencing data by modeling different read types, enabling more accurate isoform analysis at single-cell resolution...

Roche announces the launch of AXELIOS 1, a transformative next-generation sequencing platform

RNA sequencing capabilities are expanding with Roche's AXELIOS 1 platform, offering faster, scalable sequencing to support genomics research, single-cell studies, and future clinic...

Making DNA on a semiconductor chip

Researchers set a new benchmark for enzymatic DNA synthesis by writing 64 distinct sequences in parallel on a semiconductor chip.

Alithea Genomics launches early access program for MERCURIUSâ„¢ 1536 DRUG-seq, bringing transcriptomics to compound scre...

MERCURIUSâ„¢ 1536 DRUG-seq brings RNA sequencing to large-scale compound screening, enabling efficient gene expression profiling... The post Alithea Genomics launches early access...

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...

BINSEQ: A family of high-performance binary formats for nucleotide sequences

by Noam Teyssier, Alexander Dobin Modern genomics produces billions of sequencing records per run, which are typically stored as gzip-compressed FASTQ files. While this format is...

Partnership with Oxford Nanopore Technologies will support development of RNA liquid biopsy for cancer early detection

RNA sequencing and nanopore sequencing enabled Eclipse-like full transcriptome analysis to identify novel non-coding RNA biomarkers in extracellular vesicles for early esophageal.....

NanoncRNA-seq – an rRNA-depleted full-length transcriptome strategy for identification of novel lncRNA isoforms

A new RNA sequencing workflow using nanopore technology improves full-length lncRNA isoform discovery, revealing many previously undetected transcripts missed by conventional short...

D&D‑seq Uses Base Editing to Map DNA–Protein Interactions in Single Cells

D&D‑seq uses a base editor–nanobody fusion to record DNA–protein contacts at single‑cell resolution. The method maps transcription factor and chromatin-remodeling proteins. The...

miND standardizes small RNA sequencing analysis for biomarker discovery

RNA sequencing with the miND pipeline supports standardized small RNA analysis for biomarker discovery across tissues, plasma, extracellular vesicles, and other sample types...

Chimeric RNAs expand the potential of RNA sequencing for disease detection

RNA sequencing combined with the ChiTaRS platform improves detection of disease associated chimeric RNAs, supporting biomarker discovery, liquid biopsy, and precision medicine...

STGBench – sequencing-level spatial DNA-RNA simulation for multimodal and virtual cell-oriented benchmarking of genomic...

STGBench generates realistic paired DNA and RNA sequencing datasets with known genetic alterations, enabling accurate benchmarking of spatial genomics and transcriptomics analysis....

TAP-seq – targeted single-cell RNA and perturbation sequencing

TAP-seq combines genome editing with targeted RNA sequencing to enable sensitive and cost-effective single-cell functional genomics screens...

Validating RNA sequencing for reliable detection of plant viruses and viroids

A validated RNA sequencing workflow demonstrates reliable detection of plant viruses and viroids, supporting accurate, comprehensive diagnostics for symptomatic crop samples... The...

Illumina names new commercial, legal chiefs as sequencing business shows signs of stability

Illumina has filled two key C-suite posts, naming Mike Sullivan as chief commercial officer and Julie Coletti as chief legal officer as the DNA sequencing giant works to keep its t...

New eBook | RNA-seq: A peek inside the transcriptome

This collection highlights how RNA sequencing is advancing transcriptomics research, from single-cell analysis and disease mechanisms to nanopore sequencing and AI-driven data inte...

Transcriptomics in space, an RNA sequencing pipeline for space biology research

RNA sequencing supports space biology research by enabling transcriptome-wide analysis of gene expression changes associated with spaceflight and adaptation to space environments.....

Semiconductor Chip Writes DNA Sequences in Parallel

What if a computer chip could manufacture DNA? Researchers have now used semiconductor technology to write dozens of genetic sequences simultaneously. Researchers at Harvard Univer...

Whole RNA sequencing improves gene fusion detection in acute leukemia

RNA sequencing enabled comprehensive detection of clinically relevant gene fusions in acute leukemia, including rare rearrangements that conventional diagnostic methods failed to i...