patchper

tensorflow

An Open Source Machine Learning Framework for Everyone

CLOSE

Cna and LOh analysis with SEquencing data

fermi-lite

Standalone C library for assembling Illumina short reads in small regions

graphene

GraphQL framework for Python

Jellyfish

A fast multi-threaded k-mer counter

glutton

A web client for aria2

playground

Play with neural networks!

caffe

Caffe: a fast open framework for deep learning.

xgboost

Scalable, Portable and Distributed Gradient Boosting (GBDT, GBRT or GBM) Library, for Python, R, Java, Scala, C++ and more. Runs on single machine, Hadoop, Spark, Dask, Flink and DataFlow

easyjs

A simple javascript library

musicbox

网易云音乐命令行版本

dockerlite

Lightweight virtualization system based on LXC and BTRFS. See dotcloud/docker.

cyvcf2

cython + htslib == fast VCF and BCF processing

bcbio-nextgen-vm

Run bcbio-nextgen genomic sequencing analyses using isolated containers and virtual machines

kallisto

Near-optimal RNA-Seq quantification

3DS-ARM9LoaderHax-Guide

利用arm9loaderhax实现3DS自制系统的完整教程

Glowstone

A fast, customizable and compatible open source server for Minecraft: Java Edition

Lighter

Fast and memory-efficient sequencing error corrector

canvas

Canvas - Copy number variant (CNV) calling from DNA sequencing data

pdf-smart-crop

THetA

Tumor Heterogeneity Analysis (THetA) and THetA2 are algorithms that estimate the tumor purity and clonal/subclonal copy number aberrations directly from high-throughput DNA sequencing data. This repository includes the updated algorithm, called THetA2.

sequenceserver

Intuitive graphical web interface for running BLAST bioinformatics tool (i.e. have your own custom NCBI BLAST site!)

cnvkit

Copy number variant detection from targeted DNA sequencing

pattern_classification

A collection of tutorials and examples for solving and understanding machine learning and pattern classification tasks

precisionFDA

precisionFDA is a cloud based platform that provides an environment where the community can test, pilot, and benchmark new approaches to validating their next-generation sequencing (NGS) analysis pipelines. PrecisionFDA offers community members a secure and independent work area where, at their discretion, their bioinformatics tools or data can be kept private or shared with the precisionFDA participants.

go

The Go programming language

rust-cross

Everything you need to know about cross compiling Rust programs!

mt7601u

Ralink Wireless Adapter Driver

gatk-protected

Official code repository for GATK versions 1.0 through 3.7 (full licensed package). For GATK 4 code, see the https://github.com/broadinstitute/gatk repository

sleuth

Differential analysis of RNA-Seq