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Artificial Intelligence Drug Design Tutorial, 人工智能药物设计教程
Highly Open Workflow for Annotation & Ranking toward genomic variant Discovery
A pipeline approach that automatically integrates diverse biomedical data-bases to enable semantic exploration of genetic variants in disease association
Flexible, uncertainty-aware variant calling with parameter free filtration via FDR control.
A CMD script to crack password protected ZIP, RAR, 7z and PDF files, using JohnTheRipper.
Find the password of protected ZIP files.
DeepSurv is a deep learning approach to survival analysis.
Trained model and inference code for early triage of critically-ill COVID-19 patients.
A Tree based feature selection tool which combines both the Boruta feature selection algorithm with shapley values.
Provider for Chinese Tms Service
Repo for my personal site
Apache Superset is a Data Visualization and Data Exploration Platform
Deep-Learning framework for multi-omic and survival data integration
A dummy's guide to setting up (and using) HPC clusters on Ubuntu 22.04LTS using Slurm and Munge. Created by the Quant Club @ UIowa.
📦🚀 Fully automated version management and package publishing
The commitizen command line utility. #BlackLivesMatter
GeneMANIA helps you predict the function of your favourite genes and gene sets.
Full stack, modern web application template. Using FastAPI, React, SQLModel, PostgreSQL, Docker, GitHub Actions, automatic HTTPS and more.
This tools counts the number of specific k-mers within sequence data. The counts can then be compare to other counts to determine to compute the probability that sample are of the same origin to di…
Create "haplotype maps" of variants in order to use with Picardtools Crosscheck_Files utility, which allows for robust genotyping of functional genomic data.
Wrapper and analysis scripts for RNA variant calling pipeline
bioinfo-chru-strasbourg / vcf2circos
Forked from CJinny/PCircospython plotly Circos from VCF