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Single-cell and single-embryo RNA sequencing enables detailed analysis of gene expression and cell identity during the earliest stages of embryonic development...
Creative Biolabs expands RNA sequencing and multi-omics services to profile individual cells and nuclei, supporting biomarker discovery...
RNA sequencing references combined with CellART help identify individual cells and cell types within high-resolution spatial transcriptomics data across multiple...
Researchers developed recordanelles that preserve gene expression histories for days, allowing single-cell RNA sequencing to detect transient cellular responses that conventional m...
Live-cell RNA sequencing uses engineered virus-like particles to repeatedly sample transcriptomes without destroying cells, enabling researchers to track gene expression changes ov...
GARAGE uses artificial intelligence to generate realistic single-cell RNA sequencing data, improving rare cell representation, gene selection and cell clustering in complex biologi...
Scientists have built a search engine that can scan data from millions of single cells from thousands of experiments worldwide in seconds. The tool makes it possible to answer prev...
RNA sequencing data provide a real-world framework for comparing differential transcript usage methods across bulk, single-cell, spatial, long-read, and short-read transcriptomics....
RNA sequencing analysis with scFlowReport integrates differential expression, pathway enrichment, regulatory networks and cell communication into a reproducible workflow for compar...
Single-cell RNA sequencing links somatic mutations with cell states, helping researchers trace clonal evolution and identify phenotypes associated with cancer progression and treat...
POND-seq enables non-destructive RNA sequencing of living cells, allowing repeated measurement of transcriptomes and RNA-binding protein interactions as cells respond to changing c...
RNA sequencing combined with new AI models helps researchers analyze cellular relationships and biological patterns across scales, improving interpretation of complex single-cell a...
RNA sequencing combined with Cell2space reconstructs spatial domains and cell neighborhoods, helping researchers recover tissue organization lost during single-cell sample preparat...
RNA Variant Imaging is attracting attention because it addresses a persistent blind spot in cancer diagnostics: many clinically relevant RNA isoforms, splice events, and fusion tra...
Malva enables ultrafast, reference-free searches across massive single-cell RNA sequencing datasets for mutations, splice junctions, pathogens, transcripts, and other sequence-leve...
RNA sequencing efforts from the Human RNome Project aim to build a comprehensive reference of human RNA sequences, isoforms, processing states and chemical modifications...
RNA sequencing at single-cell resolution reveals cellular diversity in the Aedes aegypti midgut and provides a method for investigating mosquito responses to pathogens...
CellDiffusion improves single-cell RNA sequencing data integration by correcting batch effects while preserving cell identities and developmental trajectories, enhancing clustering...
RNA sequencing can read Detectron-generated DNA barcodes, enabling scalable detection of specific RNA signals associated with infection, gene activity and other cellular processes....
Single-cell RNA sequencing combined with GP-DHT helps predict transcription factor and target gene relationships, providing a...
Single-nucleus RNA sequencing reveals cell-specific immune responses to white spot syndrome virus in whiteleg shrimp, identifying genes that may support future disease-resistance s...
ResolVI improves spatial RNA sequencing analysis by correcting RNA assignment errors and technical variation, helping researchers distinguish cell states and detect subtle gene exp...
A new framework adapts RNA sequencing analysis for Record-seq, improving spacer extraction, transcription-unit quantification, normalization, differential expression, and modeling...
A new RNA sequencing analysis method uses the Lomb-Scargle periodogram to efficiently identify genes associated with pseudotime across complex single-cell trajectories...
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