Wellcome Sanger Institute - NPG

Login: wtsi-npg

Company: null

Location: Cambridge UK

email:

Blog: www.sanger.ac.uk

Members

  1. Jennifer Liddle
  2. Keith James
  3. Kevin Lewis
  4. Ruben E. Bautista
  5. null
  6. null
  7. null

Repositories

AnyEvent-RabbitMQ
An asynchronous and multi channel Perl AMQP client.
bambamc
lightweight C implementation of name collating BAM file input and BAM file output
bambi
A set of programs to manipulate SAM/BAM/CRAM files, using HTSLIB
baton
iRODS client programs and API
bcviz
JavaScript visualisation for bamcheck file format
biobambam
Tools for bam file processing
bwa
Burrows-Wheeler Aligner
crammer
Reference-based compression of SRA data
dalliance
Interactive web-based genome browser.
disposable-irods
Scripts to create a minimal, disposable IRODS as a test platform
freebayes
Bayesian haplotype-based polymorphism discovery and genotyping.
genotype-call
Explore the contents of Illumina's binary Genotype Call files
genotyping
Components of the WTSI genotype analysis pipeline.
Gftools
A set of utilities to handle individual-level genotype data files
git-pom-version
Updates the version of Maven pom files using "git describe"
hp4
null
htslib
C library for high-throughput sequencing data formats
illumina2bam
Generate and process BAM files from Illumina sequencing instrument files
Illuminus
A genotype calling algorithm for the Illumina BeadArray platform
irods
Middleware for your critical data.
irods-legacy
Fork of DICE irods-legacy
irods-legacy-gclp
This repository mirrors the legacy DICE-UCSD iRODS SVN repository at this time. No pull-requests will be merged back into trunk.
irods-metadata
Description of a subset of metadata used in WTSI iRODS
ml_warehouse
Perl DBIx binding to a warehouse housing data from multiple LIM systems
npg_conda
NPG Conda recipes and tools
npg_docker
Prototypes of Docker-contained Pipelines
npg_irods
Tools for managing HTS (BAM and CRAM) format files in iRODS.
npg_ml_warehouse
Analysis results loader for the multi-lims warehouse, see ml_warehouse project for the warehouse details.
npg_qc
QC checks and metrics for Illumina NGS data
npg_qc_utils
C programs extracted from npg_qc
npg_ranger
NGS data streaming (sam, bam, cram, vcf) - pre-production
npg_sentry
null
npg_seq_common
Utilities for handling NGS data
npg_seq_melt
Operations on processed sequencing data (merges, metadata updates for the archive, etc.)
npg_seq_pipeline
Processing and analysis of data coming from Illumina sequencing machines
npg_sequencescape_warehouse
Old sequencescape warehouse: DBIx binding, loader, LIMs driver for st::api::lims
npg_tracking
WTSI Illumina sequencing instruments (HiSeq, MiSeq, GA) tracking
p4
Process and Pipe Pipeline Panacea
pb_calibration
Filter and calibration programs for Illumina BAM files
Percolate
A parallel workflow management application.
perl-dnap-utilities
WTSI DNA Pipelines Perl Utility Library
perl-irods-wrap
Perl iRODS Client Wrapper Library
perl-rabbit-wrap
Perl RabbitMQ Client Wrapper Library (deprecated)
plinktools
Process Plink genotyping files in Python
samtools
null
samtools-patches
patch files for various releases of samtools
simtools
Program to create and process SIM files
teepot
null
unveil
A very lightweight jQuery plugin to lazy load images
vcftools
A set of tools written in Perl and C++ for working with VCF files, such as those generated by the 1000 Genomes Project.
zCall
A Rare Variant Caller for Array-based Genotyping

This work is supported by the National Institutes of Health's National Center for Advancing Translational Sciences, Grant Number U24TR002306. This work is solely the responsibility of the creators and does not necessarily represent the official views of the National Institutes of Health.