CoREse

DNAMatch. Python

SimPG. A population-specific haplotype genome simulation tool developed based on pangenome data

methSV. methSV: A Long-Read-Based Framework for Profiling DNA Methylation in Structural Variation

HapKled. HapKled: a haplotype-aware structural variant calling approach for Oxford Nanopore sequencing data

kled. C++

cyberDMR. A robust and high-resolution framework for detecting differentially methylated regions (DMRs) from second and third sequencing data.

GFSeeker. Python

cuteSV-OL. cuteSV-OL: a real-time structural variation detection framework for nanopore sequencing devices

ChinaMethAtlas. A comprehensive DNA methylation atlas for the Chinese population through nanopore long-read sequencing of 106 individuals

SVDF. SVDF is a long-read-based structural variants caller uses deep learning network.

SVHunter. SVHunter is a long-read-based structural variation detection through transformer model. SVHunter can detect and genotype DEL/INS/DUP/INV/TRA.

SVPG. Pangenome-based structural variation caller

cuteHap. Haplotype-Aware Structural Variant Detector

cuteFC. Regenotyping structural variants through an accurate and efficient force-calling method

longdust. Identify long STRs, VNTRs, satellite DNA and other low-complexity regions in a genome

CREAIT. CREAIT: A open-source AI tool for everyone.

free-font. 大概是2020年最全的免费可商用字体，这里收录的商免字体都能找到明确的授权出处，可以放心使用，持续更新中...

Microsoft-Activation-Scripts. Open-source Windows and Office activator featuring HWID, Ohook, TSforge, and Online KMS activation methods, along with advanced troubleshooting.

HowToCook. Programmer's guide about how to cook at home.

Bioinformatic-resources. Python

klib. A standalone and lightweight C library

free-programming-books. :books: Freely available programming books

bgt. Flexible genotype query among 30,000+ samples whole-genome

gqt. A genotype query interface.

bcftools. This is the official development repository for BCFtools. See installation instructions and other documentation here http://samtools.github.io/bcftools/howtos/install.html

htslib. C library for high-throughput sequencing data formats

pbwt. Implementation of Positional Burrows-Wheeler Transform for genetic data

rHAT. Pacbio sequence alignment tool, please use "git clone" to copy and use the repository

gfwlist. The one and only one gfwlist here

Google-IPs. Google 全球 IP 地址库

google-ips. Google 全球 IP 地址库，按国家/地区整理并提供 npm 查询 API Google IP address list grouped by country with JSON data and query helpers.

snap. Scalable Nucleotide Alignment Program -- a fast and accurate read aligner for high-throughput sequencing data