LeafLiu

Tvlist-awesome-m3u-m3u8

直播源相关资源汇总 📺 💯 IPTV、M3U —— 勤洗手、戴口罩，祝愿所有人百毒不侵

dootask

DooTask是一款开源在线项目任务管理工具，提供各类文档协作工具、在线思维导图、在线流程图、项目管理、任务分发、即时IM，文件管理等工具；同时消息功能使用非对称加密技术让你的沟通更安全。

iptv-m3u-maker

IPTV 国内+国外 电视台直播源m3u文件, 收集&汇总&本地源脚本

single-cell-tutorial

Single cell current best practices tutorial case study for the paper:Luecken and Theis, "Current best practices in single-cell RNA-seq analysis: a tutorial"

TBtools-II

GUI/CommandLine Tool Box for biologistists to utilize NGS data.

freebayes

Bayesian haplotype-based genetic polymorphism discovery and genotyping.

single-cell-best-practices

https://www.sc-best-practices.org

multiPrime

multiPrime is a mismatch-tolerant minimal primer set design tool for large and diverse sequences (e.g. Virus). Here is a web-based version (test: http://multiPrime.cn))

AnnotSV

Annotation and Ranking of Structural Variation

Exomiser

A Tool to Annotate and Prioritize Exome Variants

VarDict

VarDict

seqr

web-based analysis tool for rare disease genomics

qiwen-file

【奇文网盘】基于Spring Boot 2 + VUE CLI@3框架开发的分布式文件管理系统--后台

Apollo

Genome annotation editor with a Java Server backend and a Javascript client that runs in a web browser as a JBrowse plugin.

open-cravat

A modular annotation tool for genomic variants

cutevariant

A standalone and free application to explore genetics variations from VCF file

CharGer

Characterization of Germline variants

AmpliconSuite-pipeline

A quickstart tool for AmpliconArchitect. Performs all preliminary steps (alignment, CNV calling, seed interval detection) required prior to running AmpliconArchitect. Previously called PrepareAA.

gvanno

Generic human DNA variant annotation pipeline

SMAca

SMN1 copy-number and sequence variant analysis from next generation sequencing data

knotAnnotSV

A simple script to create a customizable html file from an AnnotSV output.

AnnotateVariants

This is a pipeline for variant annotation in the diagnosis of rare genetic disorders. It relies on open source data and has instructions for software installs.

primer-trimming

Fast C code for identifying and removing primers and adapters

amplicnv

ampliCNV is a Python 3.x package for copy number (CNV) variation detection on whole exome sequencing (WES) data from amplicon-based enrichment technologies.

germline

A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data

Diablo_ACMG

Tool for automated classification of genetic variants according to ACMG criteria.

ampliconseq

Variant calling pipeline for amplicon sequencing data

Predict_FF

Predict fetal fraction from sequenced DNA extracted from maternal blood

D3b-autoPVS1

This is a modiifed port of the original https://github.com/JiguangPeng/autopvs1, branched from commit `7fb1be97667e5ef576f81bf2fabbddcf9a4c7594`. It was re-worked in order to work with Kids First germline annotation outputs.

Variant_Annotation