-
University of Melbourne
- Melbourne, Australia
- https://rrwick.github.io
- https://orcid.org/0000-0001-8349-0778
- @rrwick
- @[email protected]
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HERRO is a highly-accurate, haplotype-aware, deep-learning tool for error correction of Nanopore R10.4.1 or R9.4.1 reads (read length of >= 10 kbps is recommended).
🚦🧬 Binning Metagenomic Contigs via Composition, Coverage and Assembly Graphs
Python package for detection of chimerism and contamination in prokaryotic genomes.
Visualise and analyse nanopore (ONT) raw signals
Assign genotypes to Salmonella Typhi genomes based on VCF files (mapped to Typhi CT18 reference genome)
🫧🧬 From fragmented assemblies to high-quality bacteriophage genomes
Automatically exported from code.google.com/p/cdhit
A toolkit for exploring prokaryotic methylation and base modifications in nanopore sequencing
Randomly subsample sequencing reads or alignments
Standalone Python re-implementation of the POLCA polisher from MaSuRCA
Automated long-read first bacterial genome assembly tool implemented in Snakemake using Snaketool.
Correcting errors in noisy long reads using variation graphs
Langevin dynamics based tours of data, in Javascript with R wrapper.
Assemblies from HPP Year 1 production
Ploidy agnostic phasing pipeline and algorithm
Bracken (Bayesian Reestimation of Abundance with KrakEN) is a highly accurate statistical method that computes the abundance of species in DNA sequences from a metagenomics sample.
High-quality Nanopore-only genome polisher
Download FASTQ files from SRA or ENA repositories.
A modern Python application packaging and distribution tool