seandavi/RNASeqBeginnerTutorial
An introduction to RNA-seq file formats, quality control, and visualization targeted to a biologist audience
Discovered public repositories for seandavi in the GitHub catalog.
An introduction to RNA-seq file formats, quality control, and visualization targeted to a biologist audience
Code and vignettes in support of the SummerX Bioconductor course in Brazil
An example RNAseq pipeline with snakemake on the NIH biowulf cluster
An informal NCI PI Retreat about the Scientific Computing Interest Group
Javascript Heatmap viewer
File system based on the SSH File Transfer Protocol
Public repository.
Public repository.
R data package containing chimp and human brain data .cel files
Fork of https://code.google.com/p/ngs-analysis
The bridge between the NCBI Gene Expression Omnibus and Bioconductor
Bioconductor facilities for parallel evaluation (experimental)
A Variant Call Format reader for Python.
A fork of the "ruffus" pipeline program
Tools for the NIH's Helix and Biowulf system
An R data package for the COSMIC database
Tools for next-generation sequencing in use at the CCR/NCI
A JavaScript visualization library for HTML and SVG.
Collection of emacs extensions specifically collected for python development, with workflow guidelines!
A quick & dirty git-powered Sinatra wiki
NGS pipelines
python access to UCSC genomes database
Public repository.
HTML5 canvas genomic graphics library
Definitions for a reStructuredText code-block directive using pygments, and scripts to render HTML and LaTeX.
My .emacs.d directory
Convert, explore, and manipulate GFF and GTF files (used in bioinformatics) using a sqlite-based approach
Tools for producing pseudo-cgh of next-generation sequencing data
AJAX Genome Browser
The missing package manager for OS X.
Mysqldump, writing in postgresql format
Python wrapper -- and more -- for Aaron Quinlan's BEDTools (bioinformatics tools)
Software for manipulating and visualizing Complete Genomics data, with a focus on cancer
GeneTrack is a genomic data visualization software
Next Gen Sequencing Utilities
SV detection from paired end reads mapping
R package for accessing NCBI EUtilities