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RNA sequencing using nanopore direct RNA sequencing enables simultaneous analysis of native RNA molecules, transcript isoforms, RNA modifications, and poly(A) tails for comprehensi...
A new RNA sequencing workflow using nanopore technology improves full-length lncRNA isoform discovery, revealing many previously undetected transcripts missed by conventional short...
Nanopore direct RNA sequencing enables accurate, site-specific quantification of pseudouridine modifications in human ribosomal RNA, expanding opportunities for large-scale epitran...
RNA sequencing combined with nanopore technology and machine learning may streamline GMP quality control testing for mRNA therapeutics within a single workflow...
RNA sequencing and nanopore sequencing enabled Eclipse-like full transcriptome analysis to identify novel non-coding RNA biomarkers in extracellular vesicles for early esophageal.....
New England Biolabs introduces a new RNA sequencing companion module that simplifies direct native RNA sequencing with Oxford Nanopore for transcriptomics and RNA...
Oxford Nanopore Technologies won the Royal Academy of Engineering’s 2026 MacRobert Award on July 8.
segSHAPE improves RNA sequencing signal alignment and modification detection, enabling more accurate secondary structure predictions from individual RNA molecules across multiple c...
A nanopore detection method can rapidly identify individual proteins, aiding disease research, drug development, and biomarker discovery.
Researchers used DNA nanotechnology to build a synthetic membrane that mimics cell pores, enabling coordinated transport and programmable reactions inside.
..Nanopore RNA sequencing models can detect RNA modifications, but benchmark results reveal significant false positives and highlight the importance of controls for accurate epitra...
Researchers set a new benchmark for enzymatic DNA synthesis by writing 64 distinct sequences in parallel on a semiconductor chip.
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...
RNA sequencing with QutRNA2 enables faster, more accurate detection of transfer RNA modifications from direct Nanopore sequencing, supporting large scale studies of RNA biology...
Tapered silicon nanopores with SiO2 surfaces detect individual proteins faster and more clearly by focusing the electric field and reducing protein sticking.
TAP-seq combines genome editing with targeted RNA sequencing to enable sensitive and cost-effective single-cell functional genomics screens...
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...
Eclipse Bioinnovations uses RNA sequencing in eSENSE Breakâ„¢ to map RNA fragmentation at single-nucleotide resolution, helping developers understand RNA stability and structural v...
A new study introduces an innovative platform capable of accurately sizing the toxic repeat expansion mutations that drive muscular dystrophy, Huntington’s disease, and ALS.
STGBench generates realistic paired DNA and RNA sequencing datasets with known genetic alterations, enabling accurate benchmarking of spatial genomics and transcriptomics analysis....
RNA sequencing with the miND pipeline supports standardized small RNA analysis for biomarker discovery across tissues, plasma, extracellular vesicles, and other sample types...
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...
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...
by Denis V. Petrovskiy, Kirill S. Nikolsky, Vladimir R. Rudnev, Liudmila I. Kulikova, Tatiana V. Butkova, Kristina A. Malsagova, Arthur T. Kopylov, Anna L. Kaysheva Proteomics uti...
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