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Bioinformatics

Publication
Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis
May 2 2025
Video
Ultra-rich human data — variant analysis with EPI2ME
September 17 2024
Video
Ultra-fast, deep-learned CNS tumour classification during surgery
May 24 2024
Bioinformatics tool
Trans-NanoSim characterizes and simulates nanopore RNA-seq data
October 10 2019
Video
Single-cell characterization of transcript isoforms with long-read RNA sequencing
May 24 2024
Bioinformatics tool
Sensitive alignment using paralogous sequence variants improves long-read mapping and variant calling in segmental duplications
October 9 2020
Video
Real-time genomic characterization of pediatric acute leukemia using adaptive sampling
May 24 2024
Bioinformatics tool
pycoQC, interactive quality control for Oxford Nanopore Sequencing
February 28 2019
Video
High-quality T2T assemblies with Oxford Nanopore-only data â€” a Singaporean case study
May 19 2025
Video
NCM 2022: STRspy-ing hidden variation in forensic DNA profiles using the MinION device
December 7 2022
Video
NCM 2021: Genomic skimming on the MinION uncovers cryptic hybridisation in the buffy-tufted marmoset, one of world’s most threatened primates
December 2 2021
Video
NCM 2021: Phages, faeces, and PromethION: using nanopore to investigate the cattle slurry virome
December 2 2021
Video
NCM 2023 Singapore: Direct detection of DNA modifications in human cancer genomes
September 27 2023
Bioinformatics tool
nanoCORR – error correction tool for nanopore sequence data
June 7 2016
Bioinformatics tool
Multiplex single-molecule kinetics of nanopore-coupled polymerases
March 16 2020
Video
Modified base detection using Oxford Nanopore MinION (London Calling)
May 15 2015
Bioinformatics tool
MMMVI: Detecting SARS-CoV-2 Variants of Concern in Metagenomic Samples
June 15 2021
Bioinformatics tool
Minimap and miniasm: fast mapping and de novo assembly for noisy long sequences
February 20 2015
Video
London Calling 2023: The dark side of carrier screening: illuminating hard-to-decipher genes in common genetic disorders with nanopore sequencing
May 19 2023
Bioinformatics tool
Leveraging MinHash for Rapid Identification of Nanopore Data on Mobile Hardware
December 3 2015

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Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis

Ultra-rich human data — variant analysis with EPI2ME

Ultra-fast, deep-learned CNS tumour classification during surgery

Trans-NanoSim characterizes and simulates nanopore RNA-seq data

Single-cell characterization of transcript isoforms with long-read RNA sequencing

Sensitive alignment using paralogous sequence variants improves long-read mapping and variant calling in segmental duplications

Real-time genomic characterization of pediatric acute leukemia using adaptive sampling

pycoQC, interactive quality control for Oxford Nanopore Sequencing

High-quality T2T assemblies with Oxford Nanopore-only data â€” a Singaporean case study

NCM 2022: STRspy-ing hidden variation in forensic DNA profiles using the MinION device

NCM 2021: Genomic skimming on the MinION uncovers cryptic hybridisation in the buffy-tufted marmoset, one of world’s most threatened primates

NCM 2021: Phages, faeces, and PromethION: using nanopore to investigate the cattle slurry virome

NCM 2023 Singapore: Direct detection of DNA modifications in human cancer genomes

nanoCORR – error correction tool for nanopore sequence data

Multiplex single-molecule kinetics of nanopore-coupled polymerases

Modified base detection using Oxford Nanopore MinION (London Calling)

MMMVI: Detecting SARS-CoV-2 Variants of Concern in Metagenomic Samples

Minimap and miniasm: fast mapping and de novo assembly for noisy long sequences

London Calling 2023: The dark side of carrier screening: illuminating hard-to-decipher genes in common genetic disorders with nanopore sequencing

Leveraging MinHash for Rapid Identification of Nanopore Data on Mobile Hardware

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