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685 results

Bioinformatics

Bioinformatics tool
Yanocomp: robust prediction of m6A modifications in individual nanopore direct RNA reads
June 16 2021
Bioinformatics tool
yacrd and fpa: upstream tools for long-read genome assembly
March 2 2020
Workflow
Workflow overview: tumour-normal sequencing
July 21 2025
Workflow
Workflow overview: 24-hour human whole-genome sequencing
September 17 2025
Workflow
Workflow overview: pharmacogenomics with adaptive sampling
August 5 2025
Workflow
Workflow overview: large cohort sequencing
July 28 2025
Workflow
Workflow overview: human variant calling
April 29 2025
Bioinformatics tool
Whole Human Genome Sequencing Project
June 20 2019
Video
Whole-genome sequencing in PulseNet foodborne molecular surveillance systems
May 24 2024
Bioinformatics tool
Whole-Genome Sequencing of a Human Clinical Isolate of emm28 Streptococcus pyogenes Causing Necrotizing Fasciitis Acquired Contemporaneously with Hurricane Harvey
November 13 2017
Poster
Whole genome Nanopore DNA analysis shows that chronic corticosterone supplementation results in altered sperm DNA methylation.
May 19 2023
Poster
Whole-genome analysis of VREfm isolates with daptomycin resistance using Oxford Nanopore and Illumina sequencing
June 20 2019
Bioinformatics tool
Wengan: Efficient and high quality hybrid de novo assembly of human genomes
November 25 2019
Bioinformatics tool
WeFaceNano: a user-friendly pipeline for complete ONT sequence assembly and detection of antibiotic resistance in multi-plasmid bacterial isolates
June 7 2021
Case study
Wastewater sequencing — an early warning system for infectious disease outbreaks
November 10 2022
Publication
Wakhan: reconstruction of chromosome-scale copy number profiles of tumour genomes with long-read sequencing
December 15 2025
Bioinformatics tool
Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignment
September 24 2021
Bioinformatics tool
VIRUSBreakend: viral integration recognition using single breakends
December 11 2020
Publication
Verkko2: integrating proximity ligation data with long-read De Bruijn graphs for efficient telomere-to-telomere genome assembly, phasing, and scaffold
December 26 2024
Bioinformatics tool
Verkko: telomere-to-telomere assembly of diploid chromosomes
June 26 2022

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

yacrd and fpa: upstream tools for long-read genome assembly

Workflow overview: tumour-normal sequencing

Workflow overview: 24-hour human whole-genome sequencing

Workflow overview: pharmacogenomics with adaptive sampling

Workflow overview: large cohort sequencing

Workflow overview: human variant calling

Whole Human Genome Sequencing Project

Whole-genome sequencing in PulseNet foodborne molecular surveillance systems

Whole-Genome Sequencing of a Human Clinical Isolate of emm28 Streptococcus pyogenes Causing Necrotizing Fasciitis Acquired Contemporaneously with Hurricane Harvey

Whole genome Nanopore DNA analysis shows that chronic corticosterone supplementation results in altered sperm DNA methylation.

Whole-genome analysis of VREfm isolates with daptomycin resistance using Oxford Nanopore and Illumina sequencing

Wengan: Efficient and high quality hybrid de novo assembly of human genomes

WeFaceNano: a user-friendly pipeline for complete ONT sequence assembly and detection of antibiotic resistance in multi-plasmid bacterial isolates

Wastewater sequencing — an early warning system for infectious disease outbreaks

Wakhan: reconstruction of chromosome-scale copy number profiles of tumour genomes with long-read sequencing

Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignment

VIRUSBreakend: viral integration recognition using single breakends

Verkko2: integrating proximity ligation data with long-read De Bruijn graphs for efficient telomere-to-telomere genome assembly, phasing, and scaffold

Verkko: telomere-to-telomere assembly of diploid chromosomes

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