Statistical Rethinking Course 2026

🤖 Open‑source deep-learning-based splice‑site predictor that decodes splicing patterns across species

Code used for DeepRNAseqPaper

A short tutorial on how to use RSEM

A streamlined workflow for DNA methylation-based classification of tumours.

DNA methylation-based classification of central nervous system tumours

Every Gene Ever Annotated in published GWAS

RNA-seq for rare diseases pipeline using nextflow

Reproducibility of "Alternative start and termination sites of transcription drive most transcript isoform differences across human tissues."

🧬 gget enables efficient querying of genomic reference databases

A tool to find sequencing data and metadata from public databases.

A genome visualization python package for comparative genomics

Command-line tool for the visualization of splicing events across multiple samples

User guide, associated script, sample data for ExomeCNV R Package

OpenMendel tutorials for ASHG Workshop

Code associated with 2019 manuscript entitled "Transcript expression-aware annotation improves rare variant discovery and interpretation"

D3 JavaScript interactive visualization of genome feature (gff) files

Genome-wide investigation of non-canonical splice sites

Tool for the Quality Control of Long-Read Defined Transcriptomes

Python script to download all Springer books released for free during the 2020 COVID-19 quarantine

Cell types enrichment analysis

All Algorithms implemented in Python

A comprehensive tutorial about GWAS and PRS

A tutorial on the most important features and idioms of Scala that you need to use Spark's Scala APIs.

A simple spark standalone cluster for your testing environment purposses