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Monkol Lek's Projects

alphafold_pytorch icon alphafold_pytorch

An implementation of the DeepMind's AlphaFold based on PyTorch for research

baminfo icon baminfo

Tools created from htslib/samtools libraries

bcftools icon bcftools

This is the official development repository for BCFtools. To compile, the develop branch of htslib is needed: git clone --branch=develop git://github.com/samtools/htslib.git htslib

code-for-blog icon code-for-blog

Code for various tutorials and programs I've written about on my blog

genome_viz icon genome_viz

Tools to produce handy genome visualizations in SVG format

hstracker icon hstracker

A deck tracker and deck manager for Hearthstone on macOS

htsjdk icon htsjdk

A Java API for high-throughput sequencing data (HTS) formats.

htslib icon htslib

C library for high-throughput sequencing data formats

lumpy-sv icon lumpy-sv

lumpy: a general probabilistic framework for structural variant discovery

mosdepth icon mosdepth

fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing

picard icon picard

A set of command line tools (in Java) for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF.

pindel icon 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 icon poretools

a toolkit for working with Oxford nanopore data

prospr icon prospr

ProSPr: Protein Structure Prediction

samblaster icon samblaster

samblaster: a tool to mark duplicates and extract discordant and split reads from sam files.

samtools icon samtools

Tools (written in C using htslib) for manipulating next-generation sequencing data

seqr icon seqr

web-based analysis tool for rare disease genomics

tabix icon tabix

Note: tabix and bgzip binaries are now part of the HTSlib project.

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