Name: Steve Hartley
Type: User
Company: DCEG, National Cancer Institute, National Institutes of Health
Bio: Ph.D. Biostatistics, B.A. Computer Science.
I specialize in developing methods and software tools for use on large high-throughput sequencing datasets.
Location: Rockville, Maryland
Steve Hartley's Projects
A very basic tutorial on the use of the DnaNexus cloud computing tools.
EasyBuild is a software installation framework in Python that allows you to install software in a structured and robust way.
Convert a list of genes to a bedfile
Integrative Genomics Viewer. Fast, efficient, scalable visualization tool for genomics data and annotations
Script to automatically create and run IGV snapshot batchscripts
The JunctionSeq R package is a powerful tool for testing and visualizing differential usage of exons and splice junctions in next-generation, high-throughput RNA-Seq experiments.
A test repository
Quality of RNA-Seq Toolset
R scripts for merging SCNA event calls into discrete SCNA events. Used for the REBC analysis.
A collection of scripts generally intended for private use. Feel free to use them as inspiration, but they are generally customized for my own use and may not work as-is. WARNING WARNING WARNING: NOT FOR PRODUCTION USE.
Collection of assorted tools for processing, filtering, annotating, organizing, merging, comparing, and reformatting variant data.
Example data for use with the vArmyKnife manual
a simple C++ library for parsing and manipulating VCF files, + many command-line utilities