Watch Novogene's free, on-demand webinar: Exploring the Untranslated: RNA Sequencing Basics & the Power of lncRNA. Learn library prep, sequencing strategies & downstream lncRNA analyses. #Transcriptomics #lncRNA #RNAseq https://tinyurl.com/5bh8jexe

🔗 Artificial Intelligence in Bulk RNA-Seq: Challenges and Potential Solutions. Computational and Structural Biotechnology Journal (CSBJ). DOI: https://doi.org/10.34133/csbj.0039 📚 CSBJ - A Science Partner Journal: https://spj.science.org/journal/csbj

🔗 Artificial Intelligence in Bulk RNA-Seq: Challenges and Potential Solutions. doi.org/10.34133/csb...

📚CSBJ - A Science Partner Journal: spj.science.org/journal/csbj

#ArtificialIntelligence #MachineLearning #Bioinformatics #Genomics #RNAseq #ComputationalBiology #SystemsBiology #PrecisionMedicine

Explore community-wide gene expression with Novogene Metatranscriptome Sequencing. We profile active transcripts from mixed microbial communities to reveal function, response & dynamics. #Metatranscriptomics #Microbiome #RNAseq https://tinyurl.com/6n9syaww

a close up of a man 's face with the words oops written on it Alt: Genuinely the gif I posted to slack along with the message about accidentally rewriting featureCounts in Rust.

dupRadar keeps breaking @nf-co.re #rnaseq runs. So as a bit of a joke, I prompted #Claude Code + @seqera.io AI to rewrite it in Rust. My Slack message:

"I did a rust rewrite over lunch. I realize that I might have accidentally also made a super fast Rust implementation of featureCounts."

Wish you knew more about RNA Sequencing? This blog will tell you everything you need to know! https://www.fiosgenomics.com/benefits-rna-sequencing/
#rnaseq #bioinformatics #transcriptomics #datanalysis

Decode bacterial & archaeal transcriptomes with Novogene Prokaryotic RNA-seq. We enrich mRNA, deplete rRNA, and deliver strand-specific expression profiling, operon detection & regulatory insights. #ProkaryoticRNA #MicrobialTranscriptomics #RNAseq https://tinyurl.com/4njv8pjm

The #omics report in the March issue of #G3journal from @annamoyer.bsky.social and @sthyme.bsky.social presents results from a bulk #RNAseq experiment revealing changes in #zebrafish embryonic transcripts upon Gli3R-mediated inhibition of #hedgehog signaling.

🔗 buff.ly/3yT9DxU

The 🆕 #omics report in the March issue of #G3journal presents #RNAseq and phenotypic analysis from multiple #Celegans mutant strains, which facilitates the dissection of genetic epistasis mechanisms in larval starvation resistance.🪱

🔗 Read the paper: buff.ly/uhXrEmX

ATCC Genome Portal's 2026 Q1 Release is live!
New #genomics #RNAseq #methylation #AMR data!
+80 human cell lines, +7 organoids, +206 bacteria, +26 viruses, +20 fungi, including 3 new MDR strains of Candida auris (Candidozyma auris). AGP now has >3600 DNA methylation profiles too! genomes.atcc.org

We are heading to #ABRF2026 in Pittsburgh, PA (March 28-31)!

Visit us at Booth #716 to explore solutions designed to support core facilities and streamline workflows for university research labs.

Let’s connect and discuss how we can help enhance your lab’s efficiency.

#NGS #DNA #RNA #RNAseq

Capture Everything. Microbiome.

Get accurate multiomic insights from stool with DNA & RNA sample collection and preservation technologies designed to maintain microbial integrity from collection to analysis.

Learn more: https://ow.ly/rxzk50YyNGb

#Microbiome #Metagenomics #RNAseq #Multiomics

preprint: biorxiv.org/content/10.6...

code: github.com/zhengxinchan...

#Genomics #Bioinformatics #LongRead #RNAseq #population_scale #Isoform

Capture the full spectrum of RNA with Novogene Whole Transcriptome Sequencing. We profile coding & non-coding transcripts (mRNA, lncRNA, circRNA, sRNA), splice variants & regulatory networks in a single run. #RNAseq #Transcriptomics #WTS https://tinyurl.com/43ucc38p

We welcome Lorenzo Vaccaro of the Telethon Institute of Genetics and Medicine (TIGEM) to the stage now. His talk discusses genotype-phenotype single-cell transcriptomics for massively parallel assessment of genetic variants.

#VariantEffect26
#RNAseq
#AtlasOfVariantEffectsAlliance

Working with single-cell #RNAsequencing data?
Discover how bioinformatics analysis can reveal the hidden insights in your data - request our sample single-cell analysis report today at www.fiosgenomics.com/request-a-sample-report-...

#singlecell #RNAseq #bioinformatics #dataanalysis

Automation at scale - no compromise to #RNAseq performance.

At SLAS with Agilent, we presented a poster on automating the Watchmaker mRNA Library Prep Kit on Bravo NGS.

Result: manual-equivalent results, high reproducibility, no cross-contamination, 96 samples in ~7 hrs.

Detect and quantify circular RNAs with Novogene circRNA-seq. We enrich back-splice junctions, perform high-depth sequencing & advanced bioinformatics to reveal regulatory circRNAs and disease links. #circRNA #Transcriptomics #RNAseq https://tinyurl.com/ycy6f9s9

Transcriptomics / Reference-based RNA-Seq data analysis / Hands-on: Reference-based RNA-Seq data analysis Training material for all kinds of transcriptomics analysis.

💡 #KnowledgeHighlight | Tutorial: Reference-based RNA-Seq data analysis in @galaxyproject.bsky.social 💫
training.galaxyproject.org/training-mat...

Explore open-access training materials in the ERGA #KnowledgeHub ➡️ knowledge.erga-biodiversity.eu
#RNAseq #DataAnalysis #Galaxy #bioinformatics

Unlock miRNA, siRNA & piRNA profiles with Novogene small RNA-seq. We deliver precise size selection, adaptor trimming, and differential expression analysis for biomarker discovery & regulatory studies. #smallRNA #miRNA #Transcriptomics #RNAseq https://tinyurl.com/bdzk5wxc

Discover how Novogene's RNA-seq decoded neuronal, microglial & complement pathways in a lupus model, pinpointing C1q & Nr4a1 in synaptic loss. A fresh take on neuropsychiatric lupus mechanisms. #SLE #RNAseq #Neurogenomics https://tinyurl.com/3wk848fp

Reveal novel regulatory transcripts with Novogene lncRNA-seq. We provide high-accuracy identification, quantification, differential expression & target prediction using strand-specific libraries and robust bioinformatics. #lncRNA #Transcriptomics #RNAseq https://tinyurl.com/2s8nmxby

Together with Elevate Bio, we automated the Watchmaker mRNA Library Prep Kit on the Biomek i7 - delivering high-quality RNA-seq libraries across 10–200 ng input with consistent performance. Scalable, high-throughput automation without compromise.
#RNAseq #LabAutomation

I2SysBio researcher Ana Conesa @anaconesa.bsky.social published a paper about how host-microbe interactions are affected in spaceflight
#bioinformatics #RNAseq

Spring School in Bioinformatics Dates ONLINE, 8-12 June 2026 To foster international participation, this course will be held online General Topic: Understanding and Working with Next Generation Sequencing Data

Excited to announce the 9th Spring School in #Bioinformatics!
🧬Join us online 8–12 June to get hands-on experience with #NGS data: genome assembly, #RNAseq, #phylogenomics, Linux, #Docker & reproducible bioinformatics workflows

shorturl.at/ZpfxR @pacbio.bsky.social @nanoporetech.com

🔬 Choosing the right cellular deconvolution tool is key!

With so many options, it’s crucial to match your tool to your needs!
Read our blog to help you choose wisely! www.fiosgenomics.com/tool-selection-for-cellu...
#Bioinformatics #RNAseq #Deconvolution #ComputationalBiology

Profile gene expression at scale with Novogene mRNA-seq. Our high-throughput Illumina PE150 workflow ensures +Q30 quality, enabling differential expression, splicing, fusion & novel transcript discovery. #RNAseq #Transcriptomics #GeneExpression https://tinyurl.com/55sk8atz

RNAseq data analysis for Beginners 19th-20th-21st-26th-27th-28th of May 2026

Registrations are now closed for the course "RNAseq data analysis for Beginners": www.physalia-courses.org/courses-work...

Thanks everyone and see you in May

#SoldOut #RNAseq

Learn more about "Next Generation Sequencing Diagnostics for Rare Neurological Diseases” at our #SpringSchool on on May 5-7

Day 1 focuses on #NGS technologies, like bioinformatic tools, #episignatures, #RNAseq and non-coding variants.

Registration: lnkd.in/dwPKM_nT
Programme: lnkd.in/dTQ2SiTk

New study maps cellular mechanisms driving fibrosis in Crohn's Disease Researchers at the Earlham Institute, the University of Edinburgh and Heriot-Watt University have analysed gut cells to understand the drivers behind fibrosis (scarring), a common complication in Crohn’s Disease affecting 10-20% of patients.

🆕 New Study: Scientists working on a Gut Cell Atlas have conducted #singlecell #RNAseq on intestinal cells, discovering clusters of immune and endothelial cells localise around scar tissue in the submucosa. 🧬💻

➡️ buff.ly/0Y9bpZN

@uoe-igc.bsky.social @helmsleytrust.bsky.social

#CellAtlas #scRNAseq

Highlights from the Paris School. It’s been inspiring to see our DCs present their work, exchange ideas w/ leading researchers, and dive into topics ranging from AI‑driven #toxicology + #chemogenomics to #RNAseq + #materials #discovery. Thank you everyone who contributed both in person and online!