riasc's Stars
microsoft/vscode
Visual Studio Code
neovim/neovim
Vim-fork focused on extensibility and usability
zed-industries/zed
Code at the speed of thought – Zed is a high-performance, multiplayer code editor from the creators of Atom and Tree-sitter.
nlohmann/json
JSON for Modern C++
google/googletest
GoogleTest - Google Testing and Mocking Framework
llm-workflow-engine/llm-workflow-engine
Power CLI and Workflow manager for LLMs (core package)
shenwei356/seqkit
A cross-platform and ultrafast toolkit for FASTA/Q file manipulation
FrancescoXX/rustcrab
An Open Source project with everything you need to learn about Rust.
ofajardo/pyreadr
Python package to read and write R RData and Rds files into/from pandas dataframes. No R or other external dependencies required.
suhrig/arriba
Fast and accurate gene fusion detection from RNA-Seq data
GoekeLab/bambu
Reference-guided transcript discovery and quantification for long read RNA-Seq data
thegenemyers/FASTGA
Pairwise whole genome aligner
rezacsedu/XAI-for-bioinformatics
Explainable AI for Bioinformatics
virtualramblas/awesome-deep-learning-4-life-sciences
A collection of resources for Deep Learning in Python for Life Sciences (with focus on biotech and pharma).
AmpliconSuite/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.
HKU-BAL/ClairS-TO
ClairS-TO - a deep-learning method for tumor-only somatic variant calling
frankligy/SNAF
Splicing Neo Antigen Finder (SNAF) is an easy-to-use Python package to identify splicing-derived tumor neoantigens from RNA sequencing data, it further leverages both deep learning and hierarchical Bayesian models to prioritize certain candidates for experimental validation
huangnengCSU/longcallR
LongcallR is a small variant caller for single molecule long-read RNA-seq data
sheynkman-lab/Long-Read-Proteogenomics
A workflow for enhanced protein isoform detection through integration of long-read RNA-seq and mass spectrometry-based proteomics.
CFIA-NCFAD/wgscovplot
The Whole Genome Sequencing Coverage Plot (wgscovplot) is a tool to generate HTML Interactive Coverage Plot given coverage depth information, variants and DNA Gene features
mliszcz/fish-shell
The user-friendly command line shell.
ylab-hi/ScanNeo2
Snakemake-based computational workflow for neoantigen prediction from diverse sources
quira-org/README-Template
A template for your READMEs
YiLab-SC/scHolography
ouyang-lab/KARR-seq
maltesie/ChimericFragments
Julia tool for the analysis and visualization of RNA-seq experiments producing chimeric reads.
PavelBashtrykov/RepEnTools
riasc/RNAnue
RNAnue
rnajena/RNAswarm
RNAswarm is a nextflow pipeline for differential RNA-RNA interaction analysis using RNA cross-linking methodologies
robinjugas/ProcaryaSV
An ensemble structural variant calling pipeline driven by snakemake using multiple SV and CNV callers.