WANGyujian123's Stars
danjweiner/AMM21
Command-line tool to run Abstract Mediation Model (Weiner et al 2022, AJHG)
ajaynadig/bhr
Suite of heritability and genetic correlation estimation tools for exome-sequencing data
choishingwan/PRSice
A software package for calculating, applying, evaluating and plotting the results of polygenic risk scores
Mikoto10032/AutomaticWeightedLoss
Multi-task learning using uncertainty to weigh losses for scene geometry and semantics, Auxiliary Tasks in Multi-task Learning
FINNGEN/saige-pipelines
saigegit/SAIGE
Development for SAIGE and SAIGE-GENE(+)
weizhouUMICH/SAIGE
xihaoli/STAAR
An R package for performing STAAR procedure in whole-genome sequencing studies
neurogenomics/MAGMA_Celltyping
Find causal cell-types underlying complex trait genetics
aertslab/scenicplus
SCENIC+ is a python package to build gene regulatory networks (GRNs) using combined or separate single-cell gene expression (scRNA-seq) and single-cell chromatin accessibility (scATAC-seq) data.
jianyangqt/gcta
GCTA software
morris-lab/CellOracle
This is the alpha version of the CellOracle package
jbryois/LDSC_nf
partitioned LDSC pipeline with nextflow
NathanSkene/EWCE
Expression Weighted Celltype Enrichment. See the package website for up-to-date instructions on usage.
jbryois/scRNA_disease
Code for our paper: https://www.biorxiv.org/content/10.1101/528463v1
bulik/ldsc
LD Score Regression (LDSC)
aertslab/pySCENIC
pySCENIC is a lightning-fast python implementation of the SCENIC pipeline (Single-Cell rEgulatory Network Inference and Clustering) which enables biologists to infer transcription factors, gene regulatory networks and cell types from single-cell RNA-seq data.
aertslab/SCENIC
SCENIC is an R package to infer Gene Regulatory Networks and cell types from single-cell RNA-seq data.
csbg/pnet_robustness
Reliable interpretability of biology-inspired deep neural networks
shap/shap
A game theoretic approach to explain the output of any machine learning model.
marcoancona/DeepExplain
A unified framework of perturbation and gradient-based attribution methods for Deep Neural Networks interpretability. DeepExplain also includes support for Shapley Values sampling. (ICLR 2018)
epigen/KPNN
Knowledge-primed neural networks
gao-lab/GLUE
Graph-linked unified embedding for single-cell multi-omics data integration
sunyolo/DeepTFni
A VGAE-based model to infer transcription factor regulatory network
rounakdey/FastSparseGRM
Efficiently calculate ancestry-adjusted sparse GRM
li-lab-genetics/favorannotator-rap
An app for automatically functionally annotating the variants of whole-genome/whole-exome sequencing (WGS/WES) studies and integrating the functional annotations with the genotype data using FAVORannotator in UK Biobank RAP
xihaoli/STAARpipelineSummary
An R package for summarizing and visualizing association analysis results of whole-genome/whole-exome sequencing (WGS/WES) studies generated by STAARpipeline
xihaoli/STAARpipeline-Tutorial
The tutorial for performing single-/multi-trait association analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using FAVORannotator, STAARpipeline and STAARpipelineSummary
li-lab-genetics/staarpipelinesummary_indvar-rap
An app for summarizing association analysis results of whole-genome/whole-exome sequencing (WGS/WES) studies in UK Biobank RAP
li-lab-genetics/staarpipelinesummary_varset-rap
An app for summarizing association analysis results of whole-genome/whole-exome sequencing (WGS/WES) studies in UK Biobank RAP