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RNA

Bioinformatics tool
Yanocomp: robust prediction of m6A modifications in individual nanopore direct RNA reads
June 16 2021
Publication
Yaniv Erlich: A vision for Ubiquitous Sequencing
January 1 2014
Workflow
Workflow overview: direct RNA sequencing
September 8 2025
Publication
The whole is greater than the sum of its parts: long-read sequencing for solving clinical problems in haematology
January 23 2024
Publication
Whole genome sequencing for rapid characterization of rabies virus using nanopore technology
August 18 2023
Company news
"...we need a better name than follow through"
December 1 2016
Company news
"...a wafer thin update"
September 29 2016
Publication
Viral and bacterial profiles in endemic influenza A virus infected swine herds using nanopore metagenomic sequencing on tracheobronchial swabs
February 28 2023
Publication
Utilising nanopore direct RNA sequencing of blood from patients with sepsis for discovery of co- and post-transcriptional disease biomarkers
May 13 2025
Publication
Using long-read sequencing to detect imprinted DNA methylation
February 22 2019
Publication
Using deep long-read RNAseq in Alzheimer’s disease brain to assess clinical relevance of RNA isoform diversity
August 7 2023
Publication
Unzipped genome assemblies of polyploid root-knot nematodes reveal unusual and clade-specific telomeric repeats
February 5 2024
Poster
Unsupervised Barcode Demultiplexing
June 19 2020
Poster
Unlocking the power of haplotype-based molecular breeding using long read DNA sequencing
May 19 2023
Poster
Universal, amplicon-based sequencing method for Canine Morbillivirus (CDV)
May 28 2022
Publication
Unified metagenomic method for rapid detection of microorganisms in clinical samples
July 7 2024
Poster
Uncovering the full-length extracellular transcriptome in human blood plasma using long-read cDNA sequencing
May 28 2022
Case study
Case study: ultra-rich nanopore data offers unprecedented insights into the transcriptomes of single cells
January 17 2024
Poster
Ultra-fast and cost-effective pathogen identification and resistance gene detection in a clinical research setting using nanopore Flongle 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

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Yanocomp: robust prediction of m6A modifications in individual nanopore direct RNA reads

Yaniv Erlich: A vision for Ubiquitous Sequencing

Workflow overview: direct RNA sequencing

The whole is greater than the sum of its parts: long-read sequencing for solving clinical problems in haematology

Whole genome sequencing for rapid characterization of rabies virus using nanopore technology

"...we need a better name than follow through"

"...a wafer thin update"

Viral and bacterial profiles in endemic influenza A virus infected swine herds using nanopore metagenomic sequencing on tracheobronchial swabs

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

Using long-read sequencing to detect imprinted DNA methylation

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

Unzipped genome assemblies of polyploid root-knot nematodes reveal unusual and clade-specific telomeric repeats

Unsupervised Barcode Demultiplexing

Unlocking the power of haplotype-based molecular breeding using long read DNA sequencing

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

Unified metagenomic method for rapid detection of microorganisms in clinical samples

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

Case study: ultra-rich nanopore data offers unprecedented insights into the transcriptomes of single cells

Ultra-fast and cost-effective pathogen identification and resistance gene detection in a clinical research setting using nanopore Flongle sequencing

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

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