Gant61's starred repositories
Single-nuclei-epigenomic-and-transcriptomic-landscape-in-Alzheimer-disease
Single-nuclei RNA-seq and ATAC-seq in Alzheimer's disease
epigraphdb-pqtl
This is the github repository to provide the R scripts been used in the phenome-wide Mendelian randomization study of plasma proteome.
RNA-seq_notes
A continually expanding collection of RNA-seq tools
createUKBphenome
Create a PheWAS code based phenome using ICD9 and ICD10 data from baskets of the UK biobank
HumanKidney_eQTL_and_snATAC-seq
codes used in the human kidney eQTL(cf) and eQTL(ci) and snATAC-seq data
AnnotateVariants
This is a pipeline for variant annotation in the diagnosis of rare genetic disorders. It relies on open source data and has instructions for software installs.
rpkm_rnaseq_count
RPKM for RNASeq counts
obesity_femrepr_MR
Code for analyses in "Obesity and risk of female reproductive disorders: A Mendelian Randomisation Study"
Kidney_Epi_Pri
Kidney Epigenome and Transcriptome-based multi-stage Prioritization
wgs_sample_preparation
Trim, Align to genome, Deduplicate, Realign WGS sequencing samples
hawe2021_meQTL_analyses
Code for the meQTL analyses presented in Hawe et al. 2021 Nature Genetics
CKD_cancer_MR
The impact of kidney function and albuminuria on risk of 19 site-specific cancers: A Mendelian randomization study
compute-grs
A small Perl script for computing genetic risk scores for obesity from a VCF file
gene-targeted-drugs
Finding gene targeted drugs for various diseases through ML methods
GWAS-scRNAseq-Integration
A Shiny tool to define the cell-type of action by integrating single cell expression data with GWAS