Monkol Lek (monkollek)

monkollek

Geek Repo

Company:Yale University

Location:New Haven, CT

Home Page:http://leklab.org

Twitter:@theFourier2k

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Monkol Lek's repositories

alphafold_pytorch

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

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Arcane-Tracker

An automatic Hearthstone tracker for Android

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baminfo

Tools created from htslib/samtools libraries

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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

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breakdancer

SV detection from paired end reads mapping

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code-for-blog

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

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genome_viz

Tools to produce handy genome visualizations in SVG format

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HSTracker

A deck tracker and deck manager for Hearthstone on macOS

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htsjdk

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

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htslib

C library for high-throughput sequencing data formats

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lumpy-sv

lumpy: a general probabilistic framework for structural variant discovery

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mito_browser

JavaScript tools for exploring variant data

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mosdepth

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

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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.

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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.

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poretools

a toolkit for working with Oxford nanopore data

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prospr

ProSPr: Protein Structure Prediction

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recessiveStats

repository for analysis of recessive genes

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samblaster

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

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samtools

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

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scissors

Split-read aligner

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seqr

web-based analysis tool for rare disease genomics

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tabix

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

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vcfscripts

Scripts for analyzing VCF files

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verifyBamID

verifyBAMID with CRAM support

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