Skip to content
View iwatobu's full-sized avatar
Block or Report

Block or report iwatobu

Block user

Prevent this user from interacting with your repositories and sending you notifications. Learn more about blocking users.

You must be logged in to block users.

Please don't include any personal information such as legal names or email addresses. Maximum 100 characters, markdown supported. This note will be visible to only you.
Report abuse

Contact GitHub support about this user’s behavior. Learn more about reporting abuse.

Report abuse

Starred repositories

Showing results

Tutorials for the crisprVerse

TeX 10 Updated Jul 25, 2024

Pipeline for assessing the tractability of potential targets (starting from Gene IDs)

Python 21 8 Updated Jul 22, 2024

LocusCompareR is a R package with visualization tools for comparing two genetic association datasets.

R 95 17 Updated Nov 24, 2022

This repository contains slides from some of the classes I have taught in my career. The repository will be updated from time to time. If you are interested in the .tex files and other material (e.…

32 8 Updated Jul 6, 2023

Data analysis scripts for "Atlas of plasma NMR biomarkers for health and disease in 118,461 individuals from the UK Biobank".

R 7 2 Updated Dec 22, 2022

GTEx & TOPMed data production and analysis pipelines

Python 332 175 Updated Apr 6, 2024

GWAS-TWAS (Transcriptome-wide association study)-Pharmacological library integration pipeline

R 15 5 Updated Mar 30, 2021

Regional association plots

R 25 5 Updated Apr 1, 2024

Regional association plots

R 25 8 Updated Apr 1, 2024

R package for performing high dimensional multi-trait colocalization analyses using GWAS summary data

R 38 10 Updated Feb 12, 2021

Code repository for Pietzner M, Wheeler E, et al. 2021 "Mapping the proteo-genomic convergence of human diseases"

R 23 7 Updated Sep 2, 2021

Code supporting analyses in paper on fine-mapping AD loci

R 15 13 Updated Jun 28, 2021

Repo for the R package coloc

R 139 44 Updated Jul 18, 2024
HTML 1 Updated Nov 24, 2020

PhenomeXcan: mapping the genome to the phenome through the transcriptome

Jupyter Notebook 11 1 Updated Jun 28, 2020

Graph-linked unified embedding for single-cell multi-omics data integration

Python 354 50 Updated Feb 23, 2024

A bioinformatics software tool for clinical interpretation of genetic variants by the 2015 ACMG-AMP guideline

Python 185 92 Updated May 28, 2023

Fine-mapping pipeline for Open Targets Genetics

Python 24 8 Updated Sep 6, 2022

Colocalisation pipeline for Open Targets Genetics

Python 15 8 Updated Apr 8, 2022

Harmonise GWAS summary statistics against a reference VCF

Python 37 6 Updated Jun 15, 2021

Manuscript code for our paper: bit.ly/bloodcellgwas

R 4 4 Updated Jun 30, 2020

A project to bootstrap EMR clusters with Hail installed

Shell 8 7 Updated Mar 28, 2020

SCAVENGE is a method to optimize the inference of functional and genetic associations to specific cells at single-cell resolution.

R 76 34 Updated Sep 1, 2023

Code for GBMI trans-ancestry proteome Mendelian randomization satellite paper

R 16 6 Updated Dec 25, 2023

Converts profiling output to a dot graph.

Python 3,157 383 Updated Jul 20, 2024

Subpopulation detection in high-dimensional single-cell data

Python 59 25 Updated Oct 5, 2020

Single cell current best practices tutorial case study for the paper:Luecken and Theis, "Current best practices in single-cell RNA-seq analysis: a tutorial"

Jupyter Notebook 1,331 444 Updated Dec 11, 2022
Next