Martin Pollard's repositories
BioNanoAnalyst
BioNanoAnalyst is a tool providing GUI to assess the genome assembly quality using BioNano data.
codecarbon
mp15's working fork of codecarbon for Pull requests etc.
dorado
Oxford Nanopore's Basecaller (mp15 working copy)
FastQ-Screen
(working copy) Detecting contamination in NGS data and multi-species analysis
genomicsbench
A benchmark suite to study the performance characteristics of genomics applications
graviton-builder
CDK builder for building graviton hosts for the benchmark suite
hapdup
Pipeline to convert a haploid assembly into diploid (working copy)
nf-core_configs
working fork of NF cores Config files used to define parameters specific to compute environments at different Institutions
npg_seq_pipeline
Processing and analysis of data coming from Illumina sequencing machines
npg_tracking
WTSI Illumina sequencing instruments (HiSeq, MiSeq, GA) tracking
perl-irods-wrap
Perl iRODS Client Wrapper Library
py-cpuinfo
A module for getting CPU info with pure Python (working tree)
pybedtools
Python wrapper -- and more -- for Aaron Quinlan's BEDTools (bioinformatics tools)
sniffles_circos
A way to make a CIRCOS plot of Sniffles BED files
tombo
Private fork of Tombo is a suite of tools primarily for the identification of modified nucleotides from raw nanopore sequencing data.
VariantWorks
Deep Learning based variant calling toolkit - https://clara-parabricks.github.io/VariantWorks/
webatlas-app
(fork for edits only) An application to display spatial and single-cell experiment data. Built in React, on the Vitessce framework.
whatshap
(private dev repo) Read-based phasing of genomic variants, also called haplotype assembly
WSL2-Linux-Kernel
The source for the Linux kernel used in Windows Subsystem for Linux 2 (WSL2)