Detecting genome structural variants with deep learning in single molecule sequencing
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Updated
Apr 9, 2025 - Python
Detecting genome structural variants with deep learning in single molecule sequencing
Sensitive and Fast Alignment Search Tool for Long Read sequencing Data.
Full-Length RNA Analysis pipeline developted by BGI RD group.
High accuracy single molecule Nanopore reads using the MrHAMER pipeline
Tools for working with single-molecule footprinting data
Preparatory demultiplex algorithms and HPC+Slurm solutions on BAM files for the ONT PGx workflow
Useful tools for Full-Length RNA analysis.
Preparatory FastQ extraction and alignment on per-sample BAM files for CypScope
Org GitHub Page init
Longevity sensing-and-intervention platform: biobutton wearables, perturb-seq screens, mtDNA biomarkers, and real-world data into a single longitudinal aging study.
ONT Dorado basecaller Orchestration Pipeline
Extremely fast and accurate Nanopore demultiplexing
The SMA-seq workflow for Oxford Nanopore Technology, in pure Python and SQLite database.
Sequencing sample sheet generator for wet lab
💫 Toolkit to help you get started with Spec-Driven Development
A benchmarking effort of various doraro models for the SMS pipeline
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