snewhouse/glu-genetics
Automatically exported from code.google.com/p/glu-genetics
Discovered public repositories for snewhouse in the GitHub catalog.
Automatically exported from code.google.com/p/glu-genetics
Public repository.
A collection of useful .gitignore templates
basic walk-throughs for alignment and variant calling from NGS sequencing data
Course materials for the Data Science Specialization: https://www.coursera.org/specialization/jhudatascience/1
Gentoo Science Overlay
ad brain expression analyses of public data
Methods to integrate data from multiple genome sequencing datasets and form consensus variant calls
Extra tools and utilities for sga
The Leek group guide to data sharing
sjn data science coursera
Data Science at the Command Line
Dockerfile for speedseq
R configurations for Docker
Tools for bam file processing
Toolkit to analyze genomic variation data, built on the GATK with Clojure
An intentionally insecure RIA suitable for pen testing and security awareness trainings written in Node, Express and Angular.
Docker container for the IPython notebook
Docker Desktop enables you to create virtual desktops that can be accessed remotely. It comes with Firefox and Libreoffice already installed!
Summer Placement Project @ Wellcome Trust Sanger Instute, Hinxton
Example shiny app
Vagrant is a tool for building and distributing development environments.
The missing package manager for OS X.
Docker-compatible Vagrant base boxes
An on demand Docker virtual machine, thanks to Vagrant and boot2docker. Works great on Macs and other platforms that don't natively support the Docker daemon. Support VirtualBox, VMware, and Parallels.
Docker Cheat Sheet
Convert statistical analysis objects from R into tidy format
Software-Defined Networking tools for LXC (LinuX Containers)
Bayesian haplotype-based polymorphism discovery and genotyping.
A set of tools (in Java) for working with next generation sequencing data in the BAM (http://samtools.sourceforge.net) format.
Abstracts presented at ECCB 2014
Squash docker images to make them smaller
de novo sequence assembler using string graphs
A WGS de novo assembler based on the FMD-index for large genomes
Public repository.
BWK awk modified for biological data
Integrative Genomics Viewer. Fast, efficient, scalable visualization tool for genomics data and annotations
Blacktie: a streamlined interface to the popular tophat/cufflinks RNA-seq pipeline
Ensembl tools including the VEP
MuTect -- Accurate and sensitive cancer mutation detection
Next Generation Sequencing Pipeline (QC, Align, Calling, Annotation)
FASTA/FASTQ pre-processing programs
Small utilities for working with fastq sequence files.
Validated, scalable, community developed variant calling and RNA-seq analysis
Deploy Shiny applications to ShinyApps
Public repository.
TextHunter - User Friendly Annotation and Concept Extraction Tool
Toolkit for processing sequences in FASTA/Q formats
DELLY: Structural variant discovery by integrated paired-end and split-read analysis
A repository for all of my teaching material