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301 results

Transcriptomics

Publication
Yaniv Erlich: A vision for Ubiquitous Sequencing
January 1 2014
Workflow
Workflow overview: direct RNA sequencing
September 8 2025
Workflow
Workflow overview: bulk transcriptomics
July 28 2025
Case study
Wastewater sequencing — an early warning system for infectious disease outbreaks
November 10 2022
Publication
Utilising nanopore direct RNA sequencing of blood from patients with sepsis for discovery of co- and post-transcriptional disease biomarkers
May 13 2025
Bioinformatics tool
Using SPAdes de novo assembler
June 19 2020
Video
Using nanopore sequencing for mRNA vaccine quality control: a journey from R&D to GMP
September 18 2024
Publication
Using deep long-read RNAseq in Alzheimer’s disease brain to assess clinical relevance of RNA isoform diversity
August 7 2023
Video
Unraveling gene expression patterns in pediatric germ cell tumors: a nanopore sequencing approach
September 17 2024
Poster
Unlocking Nanopore sequencing for managing food safety in the food industry
May 19 2023
Video
Unlocking isoform programs underlying brain development with long-read single-cell RNA sequencing | LC26
May 19 2026
Poster
Universal, amplicon-based sequencing method for Canine Morbillivirus (CDV)
May 28 2022
Video
Understanding the role of rRNA modifications in colorectal cancer | LC26
May 19 2026
Poster
Uncovering the full-length extracellular transcriptome in human blood plasma using long-read cDNA sequencing
May 28 2022
Bioinformatics tool
Two-pass alignment using machine-learning-filtered splice junctions increases the accuracy of intron detection in long-read RNA sequencing
May 29 2020
Publication
Transcriptome-wide profiling of alternative splicing regulators with CRISPore-seq
November 25 2025
Poster
Transcriptome-wide expression and RNA modifications with full-length native RNA and cDNA sequencing
May 20 2025
Publication
Transcriptome variation in human tissues revealed by long-read sequencing
August 3 2022
Publication
Transcriptome profiling for precision cancer medicine using shallow nanopore cDNA sequencing
February 9 2023
Publication
Transcriptome profiling of paediatric extracranial solid tumours and lymphomas enables rapid low‑cost diagnostic classification
August 21 2024

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Resource Centre

Yaniv Erlich: A vision for Ubiquitous Sequencing

Workflow overview: direct RNA sequencing

Workflow overview: bulk transcriptomics

Wastewater sequencing — an early warning system for infectious disease outbreaks

Utilising nanopore direct RNA sequencing of blood from patients with sepsis for discovery of co- and post-transcriptional disease biomarkers

Using SPAdes de novo assembler

Using nanopore sequencing for mRNA vaccine quality control: a journey from R&D to GMP

Using deep long-read RNAseq in Alzheimer’s disease brain to assess clinical relevance of RNA isoform diversity

Unraveling gene expression patterns in pediatric germ cell tumors: a nanopore sequencing approach

Unlocking Nanopore sequencing for managing food safety in the food industry

Unlocking isoform programs underlying brain development with long-read single-cell RNA sequencing | LC26

Universal, amplicon-based sequencing method for Canine Morbillivirus (CDV)

Understanding the role of rRNA modifications in colorectal cancer | LC26

Uncovering the full-length extracellular transcriptome in human blood plasma using long-read cDNA sequencing

Two-pass alignment using machine-learning-filtered splice junctions increases the accuracy of intron detection in long-read RNA sequencing

Transcriptome-wide profiling of alternative splicing regulators with CRISPore-seq

Transcriptome-wide expression and RNA modifications with full-length native RNA and cDNA sequencing

Transcriptome variation in human tissues revealed by long-read sequencing

Transcriptome profiling for precision cancer medicine using shallow nanopore cDNA sequencing

Transcriptome profiling of paediatric extracranial solid tumours and lymphomas enables rapid low‑cost diagnostic classification

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