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350 results

RNA

Publication
Contaminating plasmid sequences and disrupted vector genomes in the liver following adeno-associated virus gene therapy
January 16 2026
Publication
Twist-ONT: combining nanopore sequencing with the Twist comprehensive viral research panel
January 7 2026
Publication
RAPID: a targeted long-read RNA workflow for functional resolution of splicing variants in rare disease
January 2 2026
Publication
Nanopore-based RNA methylation profiling of a circulating lung cancer biomarker
December 16 2025
Publication
Long-read transcriptomics of a diverse human cohort reveals ancestry bias in gene annotation
December 3 2025
Publication
Nanopore direct RNA sequencing reveals METTL2A-mediated m3C sites in poly(A) RNA
October 30 2025
Publication
Decoding the human PBMC isonome: isoform-level resolution with single-cell long-read transcriptomics
October 17 2025
Poster
A multi-omic investigation of gene dysregulation in a complex chromothripsis-like translocation event using Oxford Nanopore sequencing
October 14 2025
Publication
Deep intronic SVA_E insertion identified as the most common pathogenic variant associated with Canavan disease: a diagnostic blind spot
September 22 2025
Publication
Identification of non-coding causative variant underlying Warsaw Breakage syndrome using long-read based genomic sequencing and transcriptome analysis
September 12 2025
Publication
Long-read single-cell genome, transcriptome and open chromatin profiling links genotype to phenotypes
September 9 2025
Workflow
Workflow overview: direct RNA sequencing
September 8 2025
Publication
Deregulating m6A regulators leads to altered RNA biology in glioma cell lines
August 19 2025
Publication
Isoform-level profiling of m6A epitranscriptomic signatures in human brain
August 8 2025
White paper
White paper: RNA and cDNA sequencing
July 31 2025
Getting started guide
Getting started guide: bulk transcriptomics
July 31 2025
Publication
A founder BRCA1 exonic duplication involving breakpoint in T2T reference genome-specific region results in constitutional fusion transcript
July 31 2025
Publication
Systematic characterisation of full-length RNA isoforms in human colorectal cancer at single-cell resolution
July 22 2025
Publication
RNA liquid biopsy via nanopore sequencing for novel biomarker discovery and cancer early detection
July 5 2025
Publication
Long-read DNA and RNA sequencing for inherited polyposis and colorectal cancer: cryptic intronic variants and multiple mutational mechanisms
June 26 2025

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Contaminating plasmid sequences and disrupted vector genomes in the liver following adeno-associated virus gene therapy

Twist-ONT: combining nanopore sequencing with the Twist comprehensive viral research panel

RAPID: a targeted long-read RNA workflow for functional resolution of splicing variants in rare disease

Nanopore-based RNA methylation profiling of a circulating lung cancer biomarker

Long-read transcriptomics of a diverse human cohort reveals ancestry bias in gene annotation

Nanopore direct RNA sequencing reveals METTL2A-mediated m3C sites in poly(A) RNA

Decoding the human PBMC isonome: isoform-level resolution with single-cell long-read transcriptomics

A multi-omic investigation of gene dysregulation in a complex chromothripsis-like translocation event using Oxford Nanopore sequencing

Deep intronic SVA_E insertion identified as the most common pathogenic variant associated with Canavan disease: a diagnostic blind spot

Identification of non-coding causative variant underlying Warsaw Breakage syndrome using long-read based genomic sequencing and transcriptome analysis

Long-read single-cell genome, transcriptome and open chromatin profiling links genotype to phenotypes

Workflow overview: direct RNA sequencing

Deregulating m6A regulators leads to altered RNA biology in glioma cell lines

Isoform-level profiling of m6A epitranscriptomic signatures in human brain

White paper: RNA and cDNA sequencing

Getting started guide: bulk transcriptomics

A founder BRCA1 exonic duplication involving breakpoint in T2T reference genome-specific region results in constitutional fusion transcript

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

RNA liquid biopsy via nanopore sequencing for novel biomarker discovery and cancer early detection

Long-read DNA and RNA sequencing for inherited polyposis and colorectal cancer: cryptic intronic variants and multiple mutational mechanisms

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