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A curated list of resources for using LLMs to develop more competitive grant applications.

Python 1,888 247 Updated Mar 1, 2024

Survival Analysis and Visualization

R 497 161 Updated Apr 8, 2024

Presentation-Ready Data Summary and Analytic Result Tables

R 1,041 114 Updated Sep 30, 2024

⛑ Code for "Metabolomic profiles predict individual multi-disease outcomes" ⛑

Jupyter Notebook 20 3 Updated Sep 27, 2022

Downstream analysis for the paper "Metabolomic profiles predict individual multi-disease outcomes in the UK Biobank cohort".

Jupyter Notebook 11 3 Updated Jun 10, 2024
R 32 5 Updated Jan 20, 2021
R 39 5 Updated Apr 5, 2021

Access share reviewed code & Jupyter Notebooks for use on the UK Biobank (UKBB) Research Application Platform. Includes resources from DNAnexus webinars, online trainings and workshops.

Jupyter Notebook 120 46 Updated Jul 30, 2024
Jupyter Notebook 56 26 Updated Jan 16, 2024

UKB RAP Notebooks contains a collection of examples of how to use UK Biobank Research Analyses Platform (RAP).

HTML 52 8 Updated Sep 17, 2024

This repo contains a JupyterLab notebook allowing individual SNPs to be filtered from the UKB genotyping data. A few approaches to filtering are provided, including options to filter by individual …

Jupyter Notebook 11 Updated Aug 21, 2023

DNAnexus platform client libraries

Python 89 85 Updated Sep 26, 2024

CellBender is a software package for eliminating technical artifacts from high-throughput single-cell RNA sequencing (scRNA-seq) data.

Python 285 52 Updated Jul 17, 2024

A Shiny web app for mapping datasets using Seurat v4

HTML 107 30 Updated Sep 24, 2024

Code used for the analysis of single nucleus RNA-seq (sNuc-Seq) data from WT and 5xFAD Alzheimer's disease mouse model, and an algorithmic approach to track changes in cell states across time.

R 4 2 Updated Jan 19, 2021

A Bayesian model for compositional single-cell data analysis

Jupyter Notebook 147 24 Updated May 2, 2023
R 2 Updated Feb 21, 2023

R package for detecting doublets in single-cell RNA sequencing data

R 403 107 Updated May 14, 2024

Methods for decontamination of single cell data

R 29 1 Updated Jan 20, 2024

R package to quantify and remove cell free mRNAs from droplet based scRNA-seq data

R 255 34 Updated Nov 1, 2022

Automatic selection of number of principal components

R 13 1 Updated Jun 27, 2022

Multi-omics view of MS postmortem white matter brain tissue

R 3 Updated May 9, 2023

A computational approach to extrapolate cell type proportion estimates using matched bulk data and cell type counts

R 3 Updated Apr 23, 2022

Single-nuclei RNA-seq and ATAC-seq in Alzheimer's disease

R 83 30 Updated Jul 1, 2021

Code for the paper 'Identifying Modifiable Risk Factors and Their Joint Effect on Dementia Prevention'

R 12 3 Updated Mar 9, 2023

R package with collection of functions created and/or curated to aid in the visualization and analysis of single-cell data using R.

R 201 21 Updated Sep 30, 2024
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