Nanopore sequence read simulator
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Updated
Mar 12, 2026 - Python
Nanopore sequence read simulator
Long read based human genomic structural variation detection with cuteSV
PEPPER-Margin-DeepVariant
CLI tool for flexible and fast adaptive sampling on ONT sequencers
Technology agnostic long read analysis pipeline for transcriptomes
De novo clustering of long transcript reads into genes
Correct mismatches, microindels, and noncanonical splice junctions in long reads that have been mapped to the genome
H.E.L.E.N. (Homopolymer Encoded Long-read Error-corrector for Nanopore)
Design degenerated primers on highly variable alignments for full genome sequencing or qPCR. Specifically developed for viruses.
Predict plasmids from uncorrected long read data
De novo construction of isoforms from long-read data
SNP-Assisted SV Calling and Phasing Using ONT
SegPore is a software to segment the raw signal of nanopore direct RNA sequencing and estimate the RNA modifications.
Wrapper to read fast5, slow5, blow5 and pod5 files.
Quality control plotting for long reads
Stand-alone tool for methylation-based discrimination of mitochondrial DNA ONT reads
Long sequencing reads classifier
An awesome Oxford Nanopore Pipeline for direct RNA-sequencing
High-performance dual barcode and primer demultiplexer for MinION sequenced reads, optimized for fungal DNA barcoding.
Snakemake workflow for the detection of vector insertion sites (VIS) in long-read sequencing data
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