Name: Alan Hoyle
Type: User
Company: UNC Lineberger Comprehensive Cancer Center
Bio: Learning Bioinformatics on the job.
Location: Chapel Hill, NC, USA
Blog: http://alanhoyle.com/
Alan Hoyle's Projects
Demonstration of a Nextflow input bug
A set of command line tools (in Java) for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF.
A lightweight parallel task engine
Open-source keyboard firmware for Atmel AVR and Arm USB families
š š£ š± Highly-accurate & wicked fast transcript-level quantification from RNA-seq reads using selective alignment
SigProfilerMatrixGenerator creates mutational matrices for all types of somatic mutations. It allows downsizing the generated mutations only to parts for the genome (e.g., exome or a custom BED file). The tool seamlessly integrates with other SigProfiler tools.
A tool for sample swap identification in high throughput sequencing studies
Steps and scripts for turning a Raspberry Pi into a useful USB drive for a Tesla
Test data to be used for automated testing with the nf-core pipelines
Python package with helper tools for the nf-core community.
A few little scripts I use on my machines.
VarDict
VarDict Java port
Convert a VCF into a MAF, where each variant is annotated to only one of all possible gene isoforms
V'DJer - B Cell Receptor Repertoire Reconstruction from short read mRNA-Seq data
Visual Studio Code