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

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A small R package to make sequencing read coverage plots in R.

HTML 42 20 Updated Apr 3, 2026

Identify which human reference genome was used to align a BAM/SAM/CRAM file

Rust 32 2 Updated Mar 28, 2026

a set of SKILLS.md for doing bioinformatics with agents like claude code

Python 536 99 Updated Apr 7, 2026

A set of ready to use Agent Skills for research, science, engineering, analysis, finance and writing.

Python 19,560 2,190 Updated Apr 27, 2026

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

Shell 9,577 1,217 Updated Apr 17, 2026

Scientific Inkscape: Inkscape extensions for figure resizing and editing

Python 907 29 Updated Apr 23, 2026

longcallR is a tool for SNP calling, haplotype phasing, and allele-specific analysis with long-read RNA-seq data.

Rust 90 8 Updated Apr 16, 2026
Python 26 1 Updated Mar 30, 2026

An efficient CLI to extract sequences from the SRA

Rust 122 12 Updated Mar 4, 2026

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

R 255 16 Updated Apr 23, 2026

R/Bioconductor interface to Sanity single-cell normalization method

R 4 2 Updated Feb 26, 2026

Visualising data frames as funky heatmaps 📊

R 198 13 Updated Dec 12, 2025
Python 35 7 Updated Apr 21, 2026

Arc Virtual Cell Atlas

Jupyter Notebook 515 51 Updated Feb 12, 2026

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

HTML 586 98 Updated Jul 21, 2025

R package to make a data frame messy and untidy.

R 154 9 Updated Aug 29, 2025

Integrative Composable Visualization Framework for ggplot2

R 392 18 Updated Jan 15, 2026

Join subcellular Visium HD bins into cells

Python 140 14 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 23,990 1,176 Updated Apr 27, 2026

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

Rust 7,309 421 Updated Apr 14, 2026

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 1,949 176 Updated Feb 8, 2026

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

Jupyter Notebook 100 5 Updated Apr 24, 2026

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

Shell 245 17 Updated Mar 28, 2026

Single-cell Case Control Analysis

R 56 12 Updated Feb 26, 2026
Jupyter Notebook 45 6 Updated Oct 30, 2024

AI model evaluation with a focus on healthcare

Jupyter Notebook 258 44 Updated Feb 18, 2026

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

Python 172 5 Updated Apr 27, 2026

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

Jupyter Notebook 23 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 73 13 Updated Oct 10, 2024

Visual exploratory analysis of gene expression data

HTML 46 15 Updated Apr 8, 2026
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