Structural variation caller using third generation sequencing
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Updated
Dec 16, 2024 - Python
Structural variation caller using third generation sequencing
A PyTorch Basecaller for Oxford Nanopore Reads
pycoQC computes metrics and generates Interactive QC plots from the sequencing summary report generated by Oxford Nanopore technologies basecaller (Albacore/Guppy)
Clair3 - Symphonizing pileup and full-alignment for high-performance long-read variant calling
PEPPER-Margin-DeepVariant
Methylation/modified base calling separated from basecalling.
Transcript discovery and quantification with long RNA reads (Nanopores and PacBio)
Identification of differential RNA modifications from nanopore direct RNA sequencing
SquiggleKit: A toolkit for manipulating nanopore signal data
Pipeline for calling structural variations in whole genomes sequencing Oxford Nanopore data
Detection of RNA modifications from Oxford Nanopore direct RNA sequencing reads (Liu*, Begik* et al., Nature Comm 2019)
Pipeline for differential gene expression (DGE) and differential transcript usage (DTU) analysis using long reads
Research release basecalling models and configurations
Comprehensive TE insertion identification with WGS/WES data from multiple sequencing technics
Snakemake pipelines for nanopore sequencing data archiving and processing
Recentrifuge: robust comparative analysis and contamination removal for metagenomics
A tool to identify, orient, trim and rescue full length cDNA reads
RNA modifications detection from Nanopore dRNA-Seq data
A versatile sequenced read processor for nanopore direct RNA sequencing
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