Monkol Lek's repositories
alphafold_pytorch
An implementation of the DeepMind's AlphaFold based on PyTorch for research
Arcane-Tracker
An automatic Hearthstone tracker for Android
breakdancer
SV detection from paired end reads mapping
code-for-blog
Code for various tutorials and programs I've written about on my blog
genome_viz
Tools to produce handy genome visualizations in SVG format
mito_browser
JavaScript tools for exploring variant data
mosdepth
fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing
pindel
Pindel can detect breakpoints of large deletions, medium sized insertions, inversions, tandem duplications and other structural variants at single-based resolution from next-gen sequence data. It uses a pattern growth approach to identify the breakpoints of these variants from paired-end short reads.
poretools
a toolkit for working with Oxford nanopore data
recessiveStats
repository for analysis of recessive genes
samblaster
samblaster: a tool to mark duplicates and extract discordant and split reads from sam files.
seqr
web-based analysis tool for rare disease genomics
vcfscripts
Scripts for analyzing VCF files
verifyBamID
verifyBAMID with CRAM support