robinvanderlee

evernote-backup

Backup & export all Evernote notes and notebooks

ANARCI

Antibody Numbering and Antigen Receptor ClassIfication

partis

B- and T-cell receptor sequence annotation, simulation, clonal family and germline inference, and affinity prediction

PandasGUI

A GUI for Pandas DataFrames

Font-Awesome

The iconic SVG, font, and CSS toolkit

svviz

Read visualizer for structural variants

samplot

Plot structural variant signals from many BAMs and CRAMs

CNView

Visualization and annotation of CNVs from population-scale whole-genome sequencing data

psb-manuscript

Manuscript source for the People of the Pacific Symposium on Biocomputing

r4ds

R for data science: a book

rstudio

RStudio is an integrated development environment (IDE) for R

osxfuse

FUSE extends macOS by adding support for user space file systems

AnnotateVariants

This is a pipeline for variant annotation in the diagnosis of rare genetic disorders. It relies on open source data and has instructions for software installs.

deeplift

Public facing deeplift repo

biopython

Official git repository for Biopython (originally converted from CVS)

JASPAR-UCSC-tracks

Code and data used to create the JASPAR UCSC Genome Browser tracks data hub

MANTA

bioinformaticsdotca.github.io

Repo for student website

GenomeAnalysisModule

Welcome to the website and github repository for the Genome Analysis Module. This website will guide the learning experience for trainees in the UBC MSc Genetic Counselling Training Program, as they embark on a journey to learn about analyzing genomes.