broadinstitute
Broad Institute Joined Sept 2010 View on GitHub
- Stars
- 15,548
- across 1,282 public repos
- Rank
- #2,469
- of 94,827 organizations, top 3%
Repositories with 50+ stars
| Rank | Repository | Language | Stars |
|---|---|---|---|
| 33,871 | Official code repository for GATK versions 4 and up | Java | 2,010 |
| 61,820 | Scientific workflow engine designed for simplicity & scalability. Trivially transition between one off use cases to massive scale production environments | Scala | 1,083 |
| 61,868 | A set of command line tools (in Java) for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF. | Java | 1,082 |
| 94,005 | Inferring CNV from Single-Cell RNA-Seq | R | 686 |
| 114,516 | Keras package for region-based convolutional neural networks (RCNNs) | Python | 553 |
| 143,794 | CellBender is a software package for eliminating technical artifacts from high-throughput single-cell RNA sequencing (scRNA-seq) data. | Python | 428 |
| 147,790 | GTEx & TOPMed data production and analysis pipelines | Python | 415 |
| 155,805 | Pilon is an automated genome assembly improvement and variant detection tool | Scala | 391 |
| 161,245 | Spatial alignment of single cell transcriptomic data. | Jupyter Notebook | 376 |
| 173,083 | Single sample Gene Set Enrichment analysis (ssGSEA) and PTM Enrichment Analysis (PTM-SEA) | R | 347 |
| 195,378 | Keras package for deep residual networks | Python | 302 |
| 212,331 | Cell type specific enhancer-gene predictions using ABC model (Fulco, Nasser et al, Nature Genetics 2019) | Python | 274 |
| 244,162 | Warp Analysis Research Pipelines | Jupyter Notebook | 232 |
| 253,273 | Estimating tumor fraction in cell-free DNA from ultra-low-pass whole genome sequencing. | R | 222 |
| 254,205 | web-based analysis tool for rare disease genomics | Python | 221 |
| 254,205 | Ultrafast GPU-enabled QTL mapper | Python | 221 |
| 264,061 | A structural variation pipeline for short-read sequencing | Python | 211 |
| 278,308 | viral-ngs: command line tools and wrappers for processing raw viral genomic data | Python | 198 |
| 298,420 | Python | 182 | |
| 322,278 | A software package for analyzing snapshots of developmental processes | Jupyter Notebook | 166 |
| 346,524 | Long read production pipelines | Jupyter Notebook | 152 |
| 364,277 | Cell Painting Gallery | 143 | |
| 377,298 | Java tools for analyzing Drop-seq data | Jupyter Notebook | 137 |
| 398,359 | What you need to process the Quarterly DepMap-Omics releases from Terra | HTML | 128 |
| 465,937 | MuTect -- Accurate and sensitive cancer mutation detection | Java | 105 |
| 465,937 | A package for designing compact and comprehensive capture probe sets. | Python | 105 |
| 469,574 | Python library for terminal color support (including 256-color support) | Python | 104 |
| 473,247 | Source code and related materials for the O'Reilly book | Jupyter Notebook | 103 |
| 476,968 | Hail helper functions for the gnomAD project and Translational Genomics Group | Python | 102 |
| 503,948 | Documentation archive for GATK tools and workflows | HTML | 95 |
| 521,203 | Explore gnomAD datasets on the web | TypeScript | 91 |
| 544,989 | HTML | 86 | |
| 566,039 | Spatial and multiomic visualization and analysis library | Jupyter Notebook | 82 |
| 583,124 | Pyro models of SARS-CoV-2 variants | Jupyter Notebook | 79 |
| 600,843 | Rails/Docker application for the Broad Institute's single cell RNA-seq data portal | Ruby | 76 |
| 607,098 | viral-ngs: complete pipelines | WDL | 75 |
| 626,802 | Fast and exact gap-affine partial order alignment | Rust | 72 |
| 640,688 | Jupyter Notebook | 70 | |
| 648,236 | Python | 69 | |
| 663,577 | GTEx Visualizations | JavaScript | 67 |
| 663,577 | Collection of analysis tools for quantitative trait loci | Python | 67 |
| 687,767 | Fast, scalable, accurate and accessible Bayesian phylogenetics | C++ | 64 |
| 732,699 | Code and data repository for the 2020 physalia course on single cell RNA sequencing. | Shell | 59 |
| 785,713 | Docker container for running the Terraform application | Shell | 54 |
| 797,173 | CLI for interacting with Cromwell servers | Python | 53 |
| 797,173 | Genomic Identification of Significant Targets in Cancer (GISTIC), version 2 | MATLAB | 53 |
| 797,173 | Scripts and utilities for analyzing tandem repeats (TRs). | Python | 53 |
| 809,287 | Tutorials, workflows, and convenience scripts for Single Cell Portal | HTML | 52 |
| 834,115 | Notebooks and scripts for reproducing analyses and figures from the V8 GTEx Consortium paper | Jupyter Notebook | 50 |
Among 94,827 organizations
10k–16k stars: 1,461 organizations, including broadinstitute
Stars along the bottom, and organizations in each band on a log scale
Where the stars are
Languages
- Python 3.6k stars, 23% · 17 repos
- Java 3.2k stars, 21% · 3 repos
- Scala 1.5k stars, 9% · 2 repos
- Jupyter Notebook 1.4k stars, 9% · 10 repos
- R 1.3k stars, 8% · 3 repos
- HTML 361 stars, 2% · 4 repos
- Shell 113 stars, 1% · 2 repos
- TypeScript 91 stars, 1% · 1 repo
and 6 more languages
When they were made
49 repos with 50+ stars, made between 2012 and 2024
Quick stats
- Next rank
- +14 stars to reach #2,468
- Next milestone
- +19,446 stars to reach the top 1%
- Public repos
- 1,282, 49 with 50+ stars
- Popular repos
- 29 over 100 stars, 3 over 1k stars
- Top repo
- gatk, #33,871 of all repos, 13% of stars
- Smaller repos
- 3,502 stars from repos under 50