oxford-nanopore
There are 75 repositories under oxford-nanopore topic.
Nextomics/NextDenovo
Fast and accurate de novo assembler for long reads
philres/ngmlr
NGMLR is a long-read mapper designed to align PacBio or Oxford Nanopore (standard and ultra-long) to a reference genome with a focus on reads that span structural variations
tjiangHIT/cuteSV
Long read based human genomic structural variation detection with cuteSV
kishwarshafin/pepper
PEPPER-Margin-DeepVariant
bcgsc/NanoSim
Nanopore sequence read simulator
LooseLab/readfish
CLI tool for flexible and fast adaptive sampling on ONT sequencers
mortazavilab/TALON
Technology agnostic long read analysis pipeline for transcriptomes
nf-core/viralrecon
Assembly and intrahost/low-frequency variant calling for viral samples
bcgsc/arcs
🌈Scaffold genome sequence assemblies using linked or long read sequencing data
kishwarshafin/helen
H.E.L.E.N. (Homopolymer Encoded Long-read Error-corrector for Nanopore)
mortazavilab/TranscriptClean
Correct mismatches, microindels, and noncanonical splice junctions in long reads that have been mapped to the genome
mortazavilab/swan_vis
A Python library to visualize and analyze long-read transcriptomes
bcgsc/HLAminer
⛏ HLA predictions from NGS shotgun data
refresh-bio/colord
A versatile compressor of third generation sequencing reads.
ksahlin/isONclust
De novo clustering of long transcript reads into genes
vpc-ccg/lordfast
Sensitive and Fast Alignment Search Tool for Long Read sequencing Data.
andrewjpage/tiptoft
Predict plasmids from uncorrected long read data
davidebolo1993/NanoR
Nanopore data analysis in R
BeatsonLab-MicrobialGenomics/micropipe
A pipeline for high-quality bacterial genome construction using ONT sequencing
jonas-fuchs/varVAMP
Design degenerated primers on highly variable alignments for full genome sequencing or qPCR. Specifically developed for viruses.
yjx1217/LRSDAY
LRSDAY: Long-read Sequencing Data Analysis for Yeasts
yekaizhou/duet
SNP-Assisted SV Calling and Phasing Using ONT
aljpetri/isONform
De novo construction of isoforms from long-read data
unique379r/strspy
STRspy: a novel alignment and quantification-based state-of-the-art method, short tandem repeat (STR) detection calling tool designed specifically for long-read sequencing reads such as from Oxford nanopore technology (ONT) and PacBio.
zhixingfeng/iGDA
Detect and phase minor SNVs from long-read sequencing data
AnjanaSenanayake/DeepSelectNet
DeepSelecNet is an enhanced deep learning model to perform read classification for selective sequencing.
bsaintjo/slow5-rs
Low level bindings and wrapper for slow5lib, an alternative for ONT Nanopore sequencing FAST5 output
HMPNK/CSA2.6
Chromosome Scale Assembler: A high-throughput chromosome scale genome assembly pipeline for vertebrate genomes
mbhall88/pistis
Quality control plotting for long reads
czmilanna/nanoforms
The repository contains the source code of the NanoForms server (Czmil et al. NanoForms: an integrated server for processing, analysis and assembly of raw sequencing data of microbial genomes, from Oxford Nanopore technology. PeerJ, 2022). It is meant to be the source for standalone server installation. https://doi.org/10.7717/peerj.13056
rnajena/read5
Wrapper to read fast5, slow5, blow5 and pod5 files.
YaoLi3/nanopore-methylation
Long sequencing reads classifier
rki-mf1/cievad
A tool suite for a simple, streamlined and rapid evaluation of variant callsets
OpenOmics/modr
An awesome Oxford Nanopore Pipeline for direct RNA-sequencing
rnajena/magnipore
Magnipore: Differential single nucleotide changes of ONT signals
simpsonlab/preqclr
preqclr is a software tool that reports on quality for long read sequencing data without the use of a reference genome.