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  • New York University School of Medicine
  • New York, NY, USA

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Showing results

Examples of my Claude Code infrastructure with skill auto-activation, hooks, and agents

Shell 7,244 943 Updated Oct 31, 2025

Scientific Inkscape: Inkscape extensions for figure resizing and editing

Python 737 23 Updated Nov 26, 2025

LongcallR is a SNP caller for single molecule long-read RNA-seq data

Rust 69 6 Updated Nov 27, 2025
Python 23 Updated Oct 1, 2025

An efficient CLI to extract sequences from the SRA

Rust 117 11 Updated Nov 18, 2025

A lightweight version of R Markdown (without using Pandoc or knitr)

R 232 13 Updated Nov 28, 2025

R/Bioconductor interface to Sanity single-cell normalization method

R 2 1 Updated Jul 24, 2025

Visualising data frames as funky heatmaps 📊

R 188 12 Updated Nov 20, 2025
Python 31 5 Updated Nov 20, 2025

Arc Virtual Cell Atlas

Jupyter Notebook 457 42 Updated May 6, 2025

💌 Create simple, beautiful personal websites and landing pages using only R Markdown.

HTML 578 96 Updated Jul 21, 2025

R package to make a data frame messy and untidy.

R 153 9 Updated Aug 29, 2025

Integrative Composable Visualization Framework for ggplot2

R 366 18 Updated Nov 15, 2025

Join subcellular Visium HD bins into cells

Python 128 12 Updated Nov 4, 2025

📦 Repomix is a powerful tool that packs your entire repository into a single, AI-friendly file. Perfect for when you need to feed your codebase to Large Language Models (LLMs) or other AI tools lik…

TypeScript 20,383 932 Updated Nov 28, 2025

A CLI tool to convert your codebase into a single LLM prompt with source tree, prompt templating, and token counting.

Rust 6,792 382 Updated Nov 24, 2025

Specify a github or local repo, github pull request, arXiv or Sci-Hub paper, Youtube transcript or documentation URL on the web and scrape into a text file and clipboard for easier LLM ingestion

Python 1,826 169 Updated Nov 14, 2025

Implements *CellAnnotator (aka *CAT/starCAT), annotating scRNA-Seq with predefined gene expression programs

Jupyter Notebook 84 3 Updated Nov 9, 2025

Download sequencing data and metadata from GSA, SRA, ENA, and DDBJ databases.

Shell 225 17 Updated Nov 20, 2025

Single-cell Case Control Analysis

R 52 11 Updated Nov 26, 2025
Jupyter Notebook 44 6 Updated Oct 30, 2024

AI model evaluation with a focus on healthcare

Jupyter Notebook 251 39 Updated Oct 15, 2025

A Python package for the identification, characterization and comparison of spatial clusters from spatial -omics data.

Python 143 4 Updated Nov 24, 2025

tools in python and R for analyzing biological count data, especially from single cell RNAseq

Jupyter Notebook 22 5 Updated Feb 1, 2024

A thorough tutorial on HLA imputation and association, accompanying our manuscript "Tutorial: A statistical genetics guide to identifying HLA alleles driving complex disease"

Jupyter Notebook 70 12 Updated Oct 10, 2024

Visual exploratory analysis of gene expression data

HTML 43 16 Updated Nov 11, 2025

R implementation of the Reshef and Rumker CNA method (https://github.com/immunogenomics/cna)

R 15 5 Updated Aug 24, 2023

Exploring dimension-reduced embeddings

HTML 111 10 Updated Jul 6, 2022

A Python toolkit for subcellular analysis of spatial transcriptomics data

Python 84 7 Updated Nov 16, 2025

A comprehensive toolkit for mutational signature analysis

Python 42 5 Updated Jul 19, 2024
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