RNA-Seq Blog

ModiDeC enables accurate detection of RNA modifications from nanopore data, helping scientists uncover how RNA shapes gene activity and disease. - @UnimedizinMainz rna-seqblog.com/modidec-a-mult…

RNA sequencing uncovered key molecular changes in 87% of cancer patients, helping guide targeted treatments that DNA tests often miss. - @SickKidsNews rna-seqblog.com/clinical-utili…

Twist Bioscience is hiring a Director of R&D to lead RNA sequencing and NGS innovation from their South San Francisco HQ. RNA-seq is key to shaping tomorrow’s genomics tools. rna-seqblog.com/director-rd-ng…

FedscGen corrects batch effects in single-cell RNA-seq data using privacy-preserving federated learning, enabling more accurate comparisons across studies. - @unihh rna-seqblog.com/fedscgen-priva…

Longcell, developed at @PennMedicine, enhances RNA sequencing accuracy for studying alternative splicing in single cells, revealing gene regulation with greater clarity than ever before. rna-seqblog.com/longcell-singl…

A new method lets scientists analyze RNA splicing and chromatin accessibility in single brain cells, even from frozen tissue, shedding light on Alzheimer’s. - @WeillCornell rna-seqblog.com/scisor-atac-co…

New RNA-seq protocol helps scientists track how Mycobacterium tuberculosis responds to antibiotics—advancing efforts to understand drug resistance and improve TB treatment. rna-seqblog.com/rna-extraction…

RNA sequencing with CompasSeq reveals how rare RNA caps change with age, shedding light on overlooked layers of gene regulation. rna-seqblog.com/compasseq-epit…

RNA sequencing reveals what makes cells unique. LMD helps scientists find key cell markers without clustering, offering clearer insights into health and disease. - @Yale rna-seqblog.com/lmd-cluster-in…

RNA sequencing helps track cell changes over time, and Sceptic boosts accuracy across diverse single-cell data, from gene expression to cell images. - @UW rna-seqblog.com/sceptic-pseudo…

CELLO-seq uses RNA sequencing to track mobile DNA in single cells, revealing how transposable elements impact development and disease. - @UniofOxford rna-seqblog.com/cello-seq-long…

RNA sequencing reveals hidden cell differences, and scGPT makes analyzing complex data easier and more accurate, even for non-coders. - @bcmhouston rna-seqblog.com/scgpt-end-to-e…

Single-cell RNA sequencing reveals how stem cells develop into specialized cells, advancing our understanding of cell fate for better regenerative medicine. - @UQ_News rna-seqblog.com/a-pluripotent-…

ENEO, a new tool from Italy’s CNR, uses tumor RNA sequencing to quickly find neoantigens for personalized cancer immunotherapy—no matched DNA data required. @CNRsocial_ rna-seqblog.com/eneo-efficient…

RNA sequencing helps decode tumor diversity at the single-cell level. New benchmarking reveals top tools for detecting copy number variations, key to understanding cancer progression and therapy response. - @LLUHealth - @NLM_NIH rna-seqblog.com/which-tool-tel…

With ExpressRM, RNA sequencing can now predict RNA modifications—no epitranscriptome data needed. This zero-shot learning model makes RNA regulation studies more accessible across tissues and diseases. rna-seqblog.com/expressrm-mult…

RNA sequencing with Oxford Nanopore reveals hidden tRNA modifications, offering new insights into diseases tied to RNA dysfunction. - @WUT_edu rna-seqblog.com/direct-rna-oxf…

RNA sequencing with IT-scC&T-seq reveals how gene regulation varies between single cells, offering new insights into chromatin structure and cell fate decisions. - @HKUniversity rna-seqblog.com/it-scct-seq-st…

Nano3P-seq improves RNA sequencing by revealing poly(A) tail dynamics across all RNA types, offering deeper insight into gene regulation. @_BIST rna-seqblog.com/nano3p-seq-cha…

A new RNA sequencing test from @UChicago detects early-stage colorectal cancer with 95% accuracy by analyzing RNA modifications in blood, offering a more sensitive tool than DNA-based tests. rna-seqblog.com/innovative-liq…