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Multiomics analysis combines data from two or more omics layers—such as genomics, transcriptomics, proteomics, and epigenomics. However, published criticisms of multiomics approach...
Published: 24 September 2026 The AMRC has today published a new spotlight report, exploring how AMRC charities are advancing genomics and supporting its use to benefit patients....
Published: September 2026 In this report, we showcase how AMRC charities are advancing genomics and supporting its use to benefit patients - from research and infrastructure to po...
A new genome-editing method, prime assembly, precisely inserts long DNA sequences into targeted genomic locations, potentially enabling mutation-agnostic gene therapies for diverse...
RNA sequencing efforts from the Human RNome Project aim to build a comprehensive reference of human RNA sequences, isoforms, processing states and chemical modifications...
Illumina is bringing its software, AI, and data offerings together in the new BioInsight platform, designed to help scientists analyze genomic and multiomic datasets. It will be sh...
The expanded next-generation sequencing offering from Clean Cells now covers GMP-compliant viral safety testing for viral vectors and recombinant preparations, building on existing...
Short-read RNA sequencing reporting the modifications that alter protein output is starting to make epitranscriptomics indispensable for patient selection in precision medicines. T...
New findings could change how scientists think about DNA organization, transcription, and genome function.
Two DNA-recording systems traced cellular family trees across mouse embryogenesis, offering new insight into how organs form and when developing cells commit to specific fates. The...
While many producers already use genetic information to help select bulls, genomic tools remain underutilised in commercial heifer selection. When used alongside phenotypic assessm...
We’re introducing AlphaGenome Atlas, a database predicting the effects of every possible single nucleotide variant in the human genome.
Google DeepMindは、ヒトゲノムで起こり得る約90億通り全ての一塩基変異の影響を事前予測したデータベース「AlphaGenome Atlas」を公開した。影響度を数値化するスコアも導入し、未解明な非コー...
Countable Labs has named Fred Hutchinson its first certified service provider, currently serving researchers across the Seattle region. And the company is continuing to build its l...
Sequencing by expansion (SBX) and Roche’s AXELIOS 1 platform introduce a new approach to single-molecule sequencing, designed to give researchers flexibility across sequencing work...
DeepMind’s latest artificial intelligence system, AlphaGenome, marks a significant leap in decoding the complexities of the human genome. With over 3 billion base pairs to analyze,...
A multi-year collaboration will connect PacBio's HiFi sequencing with Verily Pre, combining long-read genomic and clinical data for biomedical research and AI model development. Th...
RNA sequencing can read Detectron-generated DNA barcodes, enabling scalable detection of specific RNA signals associated with infection, gene activity and other cellular processes....
COVID-19 accelerated efforts to develop faster, more efficient ways of manufacturing high-quality RNA sequences. The post How COVID, Characterization, and Commerce Are Driving an R...
The atlas could help scientists decipher how genetic variation shapes health and disease. The post Google’s Genome Atlas Predicts the Effect of Every Possible DNA Mutation appeared...
The PROPEL program aims to control gene expression through RNA structure, building logic-gated RNA therapies that switch on only where and when intended, without altering the genom...
Electronic health records (EHRs) are central to patient-centered care. However, many current EHR systems do not represent, exchange, or reuse genomic findings in structured, intero...
Bulk RNA sequencing helps researchers identify gene expression patterns associated with differences in drug response, supporting biomarker discovery and personalized medicine while...
Most one-base changes to the human genome do nothing, but a few are significant.
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