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

Rust 69 6 Updated Sep 12, 2025

Annotation-free quantification of RNA splicing. Yang I. Li, David A. Knowles, Jack Humphrey, Alvaro N. Barbeira, Scott P. Dickinson, Hae Kyung Im, Jonathan K. Pritchard

R 226 123 Updated Jun 1, 2024
Shell 8 Updated May 28, 2025

Leaflet is a probabilistic model that identifies latent cell states defined by splicing changes.

Jupyter Notebook 11 1 Updated May 10, 2024

Pan-transcriptomic phenotyping

Python 19 Updated Nov 5, 2025
Python 27 1 Updated Apr 11, 2025

Summarize and filter read alignments from multiple sequencing samples (taken as sorted BAM files)

C++ 17 3 Updated Oct 12, 2025

Integrate DNA-seq and RNA-seq data to identify mutations that are associated with regulatory effects on gene expression.

C++ 132 29 Updated Aug 21, 2024

R package to estimate sharing between two arrays of p-values

C++ 1 Updated Jul 9, 2020

A tool for analyzing trascriptomes of millions of single cells.

Python 89 25 Updated Aug 12, 2025

Perform differential expression analysis on cohort-scale single cell datasets using linear mixed models

HTML 15 Updated Oct 20, 2025

Analysis code and results for dreamlet

R 9 2 Updated Jul 18, 2025

upload big files to Zenodo using cURL, jq and bash

Shell 300 43 Updated Feb 6, 2025

Demultiplexing and debarcoding tool designed for LR-Split-seq data.

Python 23 4 Updated Oct 19, 2023

Data Portal for NYGC ALS Spinal Cord

HTML 8 2 Updated Aug 30, 2023

Single cell analysis in the browser

JavaScript 152 18 Updated Oct 26, 2025

A re-analysis of the [Single-cell transcriptomic analysis of Alzheimer’s disease](https://www.nature.com/articles/s41586-019-1195-2) using a standardised data processing and pseudobulk differential…

HTML 14 4 Updated Dec 5, 2023
Jupyter Notebook 112 29 Updated Apr 24, 2024

Code repository for analysis in "Divergent impacts of C9orf72 repeat expansion on neurons and glia in ALS and FTD"

R 6 4 Updated Sep 18, 2023

Suite of heritability and genetic correlation estimation tools for exome-sequencing data

HTML 35 6 Updated Feb 26, 2025
Perl 13 1 Updated Sep 20, 2022
R 37 5 Updated Jan 20, 2021

Create curved text paths in ggplot2

R 636 25 Updated Jul 21, 2025

A tool to facilitate comparative visualisation of CLIP data

R 15 5 Updated Nov 29, 2023

An R package for creating mirrored Manhattan plots

R 18 12 Updated Sep 30, 2022

Computationally efficient and statistically powerful software for detecting context-specific eQTL effects in multi-context genomic studies.

7 3 Updated Mar 4, 2025

SNPbrowser is project written in python to display results from Genome-Wide Association Studies (GWAS) with a wide range of possibilities, including overlap of multiple studies.

R 10 1 Updated May 2, 2025

job: free Your RStudio Console

R 253 8 Updated Sep 30, 2024

Reference-guided transcript discovery and quantification for long read RNA-Seq data

R 219 24 Updated Oct 9, 2025
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