pyc1216

bamdst

a lightweight bam file depth statistical tool

rnacocktail

RNAseq-workflow

A repository for setting up a RNAseq workflow

gatk

Official code repository for GATK versions 4 and up

radia

RADIA: RNA and DNA Integrated Analysis for Somatic Mutation Detection

bcbio-nextgen

Validated, scalable, community developed variant calling, RNA-seq and small RNA analysis

snakepipes

Customizable workflows based on snakemake and python for the analysis of NGS data

TensorFlow-World

:earth_americas: Simple and ready-to-use tutorials for TensorFlow

manta

Structural variant and indel caller for mapped sequencing data

sambamba

Tools for working with SAM/BAM data

go-library

Go语言入门、Go相关优质资料等分享

bypy

Python client for Baidu Yun (Personal Cloud Storage) 百度云/百度网盘Python客户端

fgbio

Tools for working with genomic and high throughput sequencing data.

simanneal

Python module for Simulated Annealing optimization

msisensor

microsatellite instability detection using tumor only or paired tumor-normal data

deepvariant

DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.

pysam

Pysam is a Python package for reading, manipulating, and writing genomics data such as SAM/BAM/CRAM and VCF/BCF files. It's a lightweight wrapper of the HTSlib API, the same one that powers samtools, bcftools, and tabix.

bedtools2

bedtools - the swiss army knife for genome arithmetic

MHXX_SaveEditor

Anti-Anti-Spider

越来越多的网站具有反爬虫特性，有的用图片隐藏关键数据，有的使用反人类的验证码，建立反反爬虫的代码仓库，通过与不同特性的网站做斗争（无恶意）提高技术。（欢迎提交难以采集的网站）（因工作原因，项目暂停）