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杨浩's Projects

3dmol.js icon 3dmol.js

WebGL accelerated JavaScript molecular graphics library

agfusion icon agfusion

Python package to annotate and visualize gene fusions.

akt icon akt

Ancestry and Kinship Tools

arangodb icon arangodb

🥑 ArangoDB is a native multi-model database with flexible data models for documents, graphs, and key-values. Build high performance applications using a convenient SQL-like query language or JavaScript extensions.

artemis icon artemis

Artemis is a free genome viewer and annotation tool that allows visualization of sequence features and the results of analyses within the context of the sequence, and its six-frame translation

atlas-cnv icon atlas-cnv

Method to detect exonic CNVs in NGS Gene Targeted Panels

autojump icon autojump

A cd command that learns - easily navigate directories from the command line

awesome-deepbio icon awesome-deepbio

A curated list of awesome deep learning applications in the field of computational biology

awesome-django icon awesome-django

Repository mirror of GitLab: https://gitlab.com/rosarior/awesome-django

bamsurgeon icon bamsurgeon

tools for adding mutations to existing .bam files, used for testing mutation callers在一个bam文件上模拟突变,用于pipeline的性能验证

battenberg icon battenberg

Battenberg R package for subclonal copynumber estimation

bio-playground icon bio-playground

miscellaneous scripts for bioinformatics/genomics that dont merit their own repo.

biopieces icon biopieces

Biopieces is a bioinformatic framework of tools easily used and easily created.

bmsisea icon bmsisea

Detection of micro-satellite instability from circulating tumor DNA by targeted deep sequencing,燃石bMSI检测

bootstrap icon bootstrap

The most popular HTML, CSS, and JavaScript framework for developing responsive, mobile first projects on the web.

cancerlocator icon cancerlocator

A Java package for non-invasive cancer diagnosis using methylation profiles of cell-Free DNA.

cancerseekv1 icon cancerseekv1

R code for the algorithm used in Cohen et al. Science 2018 "Detection and localization of surgically resectable cancers with a multi-analyte blood test", Science 2018, 359(6378):926-930.CancerSEEKv1中计算Omega score的脚本

caveman icon caveman

SNV expectation maximisation based mutation calling algorithm aimed at detecting somatic mutations in paired (tumour/normal) cancer samples. Supports both bam and cram format via htslib

cellassign icon cellassign

Automated, probabilistic assignment of cell types in scRNA-seq data,判断单细胞转录组测序结果和数据库中的哪些类型一样。

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