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Software for FLT3-ITD detection and MRD monitoring assay
Clinical interpretation of somatic mutations in cancer
DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Blazing fast Neovim config providing solid defaults and a beautiful UI, enhancing your neovim experience.
Extremely simple yet powerful header-only C++ plotting library built on the popular matplotlib
基于大模型搭建的聊天机器人，同时支持 微信公众号、企业微信应用、飞书、钉钉 等接入，可选择GPT3.5/GPT-4o/GPT4.0/ Claude/文心一言/讯飞星火/通义千问/ Gemini/GLM-4/Claude/Kimi/LinkAI，能处理文本、语音和图片，访问操作系统和互联网，支持基于自有知识库进行定制企业智能客服。
Estimate damage in standard NGS library preparation. Incompatible with library preparation methods from which the imbalance is lost (such as transposon based methods and Ultra II FS library prepara…
Automatically exported from code.google.com/p/cdhit
A versatile pairwise aligner for genomic and spliced nucleotide sequences
Create "haplotype maps" of variants in order to use with Picardtools Crosscheck_Files utility, which allows for robust genotyping of functional genomic data.
A bioinformatics software tool for clinical interpretation of genetic variants by the 2015 ACMG-AMP guideline
Annotation of VCF variants with functional impact and from databases (executable+library)
《Python Cookbook》 3rd Edition Translation
MiXCR is an ultimate software platform for analysis of Next-Generation Sequencing (NGS) data for immune profiling.
Post-analysis of immune repertoire sequencing data
Read-based phasing of genomic variants, also called haplotype assembly
12 weeks, 26 lessons, 52 quizzes, classic Machine Learning for all
24 Lessons, 12 Weeks, Get Started as a Web Developer
10 Weeks, 20 Lessons, Data Science for All!
Use a docx as a jinja2 template