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Code for the book "Software Engineering for Data Scientists"

Jupyter Notebook 86 43 Updated Jul 15, 2025

TCR and BCR assembly from RNA-seq data

C 320 55 Updated Jul 7, 2025

pix2tex: Using a ViT to convert images of equations into LaTeX code.

Python 15,052 1,212 Updated Jan 18, 2025

Regression Modeling Strategies

R 187 52 Updated May 27, 2025

Survival package for R

R 412 111 Updated Jun 27, 2025

❗ This is a read-only mirror of the CRAN R package repository. glmnet — Lasso and Elastic-Net Regularized Generalized Linear Models. Homepage: https://glmnet.stanford.edu

C++ 91 89 Updated Jul 17, 2025

Interactive roadmaps, guides and other educational content to help developers grow in their careers.

TypeScript 332,147 42,437 Updated Jul 24, 2025

freeCodeCamp.org's open-source codebase and curriculum. Learn math, programming, and computer science for free.

TypeScript 424,139 40,947 Updated Jul 24, 2025

Circular visualization in R

R 989 151 Updated Nov 11, 2023

Python library for calling Cytoscape Automation via CyREST

Python 83 15 Updated Apr 19, 2025

Run cBioPortal using Docker Compose

Shell 19 50 Updated Jun 10, 2025

Convert a VCF into a MAF, where each variant is annotated to only one of all possible gene isoforms

Perl 391 222 Updated Dec 9, 2024

Introduction course to transcriptomics

HTML 5 2 Updated May 31, 2025

VueGen automates the creation of reports from bioinformatics outputs, supporting formats like PDF, HTML, DOCX, ODT, PPTX, Reveal.js, Jupyter notebooks, and Streamlit web applications. Users simply …

Python 24 Updated Jul 23, 2025

Single-cell RNA-Seq pipeline for barcode-based protocols such as 10x, DropSeq or SmartSeq, offering a variety of aligners and empty-droplet detection

Nextflow 281 193 Updated Jul 24, 2025

Amplicon sequencing analysis workflow using DADA2 and QIIME2

Nextflow 211 141 Updated Jul 21, 2025

Single-cell/nuclei pipeline for data derived from Oxford Nanopore and 10X Genomics

Nextflow 42 15 Updated Jul 8, 2025

RNA sequencing analysis pipeline using STAR, RSEM, HISAT2 or Salmon with gene/isoform counts and extensive quality control.

Nextflow 1,071 784 Updated Jul 24, 2025

Call and score variants from WGS/WES of rare disease patients.

Nextflow 105 48 Updated Jul 10, 2025

Project documentation with Markdown.

Python 20,776 2,515 Updated Feb 21, 2025

DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.

Python 3,456 758 Updated May 16, 2025

The Ensembl Variant Effect Predictor predicts the functional effects of genomic variants

Perl 495 157 Updated Jul 17, 2025

cBioPortal for Cancer Genomics

Java 827 695 Updated Jul 23, 2025

A simple, yet elegant, HTTP library.

Python 53,082 9,507 Updated Jul 18, 2025

This is the development home of the workflow management system Snakemake. For general information, see

Python 2,529 601 Updated Jul 24, 2025

This API provides programmatic access to the AlphaGenome model developed by Google DeepMind.

Python 1,093 118 Updated Jul 23, 2025

A complete pipeline for metagenomic analysis

Scilab 421 84 Updated Jul 14, 2025

ATLAS - Three commands to start analyzing your metagenome data

Python 393 99 Updated May 9, 2025
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