CLI tool for flexible and fast adaptive sampling on ONT sequencers
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Updated
Feb 25, 2026 - Python
CLI tool for flexible and fast adaptive sampling on ONT sequencers
Assembly and intrahost/low-frequency variant calling for viral samples
ClairS: a deep-learning method for long-read tumor–normal pair somatic small variant calling
ClairS-TO - a deep-learning method for tumor-only somatic variant calling
Clair3-RNA - a long-read small variant caller for RNA sequencing data
Mapping-based Genome Size Estimation (MGSE) performs an estimation of a genome size based on a read mapping to an existing genome sequence assembly.
Basecalling configuration prediction through FASTQ files
ITS region extraction for long-read amplicon sequencing
DDM-grade telemetry from HSGQ/ODI GPON SFP ONUs over SSH - Prometheus exporter + Grafana dashboard
A comprehensive telomere annotation tool for genome assemblies and graphs.
MegaPath-Nano: Accurate Compositional Analysis and Drug-level Antimicrobial Resistance Detection Software for Oxford Nanopore Long-read Metagenomics; MegaPath-Nano-Amplicon: filtering module for metagenomic amplicon data
Wrapper to read fast5, slow5, blow5 and pod5 files.
A comprehensive DNA methylation atlas for the Chinese population through nanopore long-read sequencing of 106 individuals
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