NanoSimNanopore sequence read simulator
Stars: ✭ 156 (+173.68%)
SNPGenieProgram for estimating πN/πS, dN/dS, and other diversity measures from next-generation sequencing data
Stars: ✭ 81 (+42.11%)
pipeline-pinfish-analysisPipeline for annotating genomes using long read transcriptomics data with pinfish
Stars: ✭ 27 (-52.63%)
taeperA small python program to simulate a real-time Nanopore sequencing run based on a previous experiment.
Stars: ✭ 18 (-68.42%)
Clair3Clair3 - Symphonizing pileup and full-alignment for high-performance long-read variant calling
Stars: ✭ 119 (+108.77%)
poreCovSARS-CoV-2 workflow for nanopore sequence data
Stars: ✭ 34 (-40.35%)
wenganAn accurate and ultra-fast hybrid genome assembler
Stars: ✭ 81 (+42.11%)
haslrA fast tool for hybrid genome assembly of long and short reads
Stars: ✭ 68 (+19.3%)
spacepharerSpacePHARER CRISPR Spacer Phage-Host pAiRs findER
Stars: ✭ 30 (-47.37%)
pepperPEPPER-Margin-DeepVariant
Stars: ✭ 179 (+214.04%)
gfapyGfapy: a flexible and extensible software library for handling sequence graphs in Python
Stars: ✭ 54 (-5.26%)
awesome-nanoporeA curated list of awesome nanopore analysis tools.
Stars: ✭ 100 (+75.44%)
deepsignalDetecting methylation using signal-level features from Nanopore sequencing reads
Stars: ✭ 90 (+57.89%)
poreplexA versatile sequenced read processor for nanopore direct RNA sequencing
Stars: ✭ 74 (+29.82%)
kalignA fast multiple sequence alignment program.
Stars: ✭ 89 (+56.14%)
TideHunterTideHunter: efficient and sensitive tandem repeat detection from noisy long reads using seed-and-chain
Stars: ✭ 15 (-73.68%)
rerioResearch release basecalling models and configurations
Stars: ✭ 60 (+5.26%)
MGSEMapping-based Genome Size Estimation (MGSE) performs an estimation of a genome size based on a read mapping to an existing genome sequence assembly.
Stars: ✭ 22 (-61.4%)
recentrifugeRecentrifuge: robust comparative analysis and contamination removal for metagenomics
Stars: ✭ 79 (+38.6%)
streamformaticsReal-time species-typing visualisation for nanopore data.
Stars: ✭ 13 (-77.19%)
tiptoftPredict plasmids from uncorrected long read data
Stars: ✭ 27 (-52.63%)
fast-sgFast-SG: An alignment-free algorithm for ultrafast scaffolding graph construction from short or long reads.
Stars: ✭ 22 (-61.4%)
rkmhClassify sequencing reads using MinHash.
Stars: ✭ 42 (-26.32%)
interARTICInterARTIC - An interactive local web application for viral whole genome sequencing utilising the artic network pipelines..
Stars: ✭ 22 (-61.4%)
IsoQuantReference-based transcript discovery from long RNA read
Stars: ✭ 26 (-54.39%)
WinnowmapLong read / genome alignment software
Stars: ✭ 151 (+164.91%)
RATTLEReference-free reconstruction and error correction of transcriptomes from Nanopore long-read sequencing
Stars: ✭ 35 (-38.6%)
nanoflow🔬 De novo assembly of nanopore reads using nextflow
Stars: ✭ 20 (-64.91%)
vbz compressionVBZ compression plugin for nanopore signal data
Stars: ✭ 31 (-45.61%)
nanoseqNanopore demultiplexing, QC and alignment pipeline
Stars: ✭ 82 (+43.86%)
pychopperA tool to identify, orient, trim and rescue full length cDNA reads
Stars: ✭ 74 (+29.82%)
chromapFast alignment and preprocessing of chromatin profiles
Stars: ✭ 93 (+63.16%)
flexidotHighly customizable, ambiguity-aware dotplots for visual sequence analyses
Stars: ✭ 73 (+28.07%)
lasagne4bioNo description or website provided.
Stars: ✭ 103 (+80.7%)
deepsignal-plantDetecting methylation using signal-level features from Nanopore sequencing reads of plants
Stars: ✭ 21 (-63.16%)
NanoRNanopore data analysis in R
Stars: ✭ 31 (-45.61%)
iGenomicsThe first app for Mobile DNA Sequence Alignment and Analysis
Stars: ✭ 33 (-42.11%)