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149 results

Gene expression

Workflow
Workflow overview: single-cell transcriptomics
February 24 2025
Video
Unraveling gene expression patterns in pediatric germ cell tumors: a nanopore sequencing approach
September 17 2024
Poster
Universal, amplicon-based sequencing method for Canine Morbillivirus (CDV)
May 28 2022
Video
Understanding the binding of multiple transcription factors by base-pair-resolution chromatin accessibility
September 17 2024
Poster
Uncovering the full-length extracellular transcriptome in human blood plasma using long-read cDNA sequencing
May 28 2022
Publication
Transcriptome profiling for precision cancer medicine using shallow nanopore cDNA sequencing
February 9 2023
Poster
Transcriptome profiling of Korean colon cancer by cDNA PCR Nanopore sequencing
September 9 2019
Poster
Transcriptome analysis using long nanopore reads
May 21 2024
Bioinformatics tool
Trans-NanoSim characterizes and simulates nanopore RNA-seq data
October 10 2019
Video
Towards routine modopathy diagnostics: advances and clinical application of direct RNA sequencing
May 19 2025
Publication
The detection, function, and therapeutic potential of RNA 2'-O-methylation
February 24 2025
Bioinformatics tool
A technology-agnostic long-read analysis pipeline for transcriptome discovery and quantification
June 18 2019
Publication
Targeting sex determination to suppress mosquito populations
November 15 2023
Bioinformatics tool
TALC: Transcription-Aware Long Read Correction
January 11 2020
Publication
Systematic characterisation of full-length RNA isoforms in human colorectal cancer at single-cell resolution
July 22 2025
Bioinformatics tool
Swan: a library for the analysis and visualization of long-read transcriptomes
September 29 2020
Poster
Successful training of laboratories in Asia and Africa to use nanopore sequencing for poliovirus surveillance
May 19 2023
Video
Studying disease-causing polymorphic transposable element insertions using nanopore sequencing
September 17 2024
Poster
Study of SPG11’s splicing, in neuronal and non-neuronal cells, by long-read sequencing: implication on phenotype
May 19 2023
Case study
Case study: solving the parent-of-origin effect in retinoblastoma to determine disease severity
April 4 2025

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Resource Centre

Workflow overview: single-cell transcriptomics

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

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

Understanding the binding of multiple transcription factors by base-pair-resolution chromatin accessibility

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

Transcriptome profiling for precision cancer medicine using shallow nanopore cDNA sequencing

Transcriptome profiling of Korean colon cancer by cDNA PCR Nanopore sequencing

Transcriptome analysis using long nanopore reads

Trans-NanoSim characterizes and simulates nanopore RNA-seq data

Towards routine modopathy diagnostics: advances and clinical application of direct RNA sequencing

The detection, function, and therapeutic potential of RNA 2'-O-methylation

A technology-agnostic long-read analysis pipeline for transcriptome discovery and quantification

Targeting sex determination to suppress mosquito populations

TALC: Transcription-Aware Long Read Correction

Systematic characterisation of full-length RNA isoforms in human colorectal cancer at single-cell resolution

Swan: a library for the analysis and visualization of long-read transcriptomes

Successful training of laboratories in Asia and Africa to use nanopore sequencing for poliovirus surveillance

Studying disease-causing polymorphic transposable element insertions using nanopore sequencing

Study of SPG11’s splicing, in neuronal and non-neuronal cells, by long-read sequencing: implication on phenotype

Case study: solving the parent-of-origin effect in retinoblastoma to determine disease severity

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