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multiomics_integration Public
Preparing scRNA-seq and scATAC-seq data in h5ad format for use as input in MultiVI to infer latent representations.
Python UpdatedDec 26, 2024 -
GRN_inference_scRNAseq Public
GRN inference by pyscenic for scRNAseq data
Python UpdatedDec 6, 2024 -
visualizes mRNA-seq data interactively.
R UpdatedNov 13, 2024 -
scMultiFlow Public
Forked from dos257/scMultiFlowDocker image for Python and R bioinformatics tools
Dockerfile UpdatedOct 9, 2024 -
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scMoMsQC Public
Forked from Rachmanichou/scMoMsQCA Python pipeline for quality control analysis and outlier detection in multisample single-cell multiomics and RNAseq.
HTML UpdatedAug 16, 2024 -
A Tensorflow-based multimodal baseline VAE model with a supervised classifier component to test on some small synthetic data incl. scRNAseq (trx read-by-cell), scATACseq (peak-by-cell) and Imaging …
Jupyter Notebook UpdatedAug 7, 2024 -
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Bayesian-PRS Public
Bayesian PRS methods model uncertainty in effect size estimates and shrink small effect sizes to mitigate spurious associations and biases from sample overlap. By using full posterior distributions…
Jupyter Notebook UpdatedAug 6, 2024 -
bam_cellsnp_bcftools_pipeline Public
Forked from nnkarma12/bam_cellsnp_bcftools_pipelineThis repository contains a collection of scripts for processing genomic data using BAM subset, cellSNP, and bcftools. The scripts facilitate various steps in the genomic data analysis pipeline, inc…
Shell UpdatedJul 17, 2024 -
GEX-analysis-scMultiomics Public
Multiomics Pipeline by Mo De for FOUNDIN-1c: RNA Analysis Only
R UpdatedJul 12, 2024 -
scPseudobulk-analysis- Public
Automated pipeline for psuedobulk analysis and downstream unsupervised analysis based on seurat v5
R UpdatedJul 12, 2024 -
NNMF-for-scRNAseq Public
Non negative matrix factorization for Oligo lineage scRNAseq data
R UpdatedJul 12, 2024 -
Pseudotime-downstream-by-ML Public
This script utilizes Monocle3 for inferring pseudotime and employs gradient boosting machine learning (xgboost) to identify genes predictive of pseudotime. Subsequently, it fits a regression model …
R UpdatedJul 12, 2024 -
sc-informed-PRS-analysis Public
single cell informed polygenic risk scoring in Parkinson's disease
R UpdatedJul 12, 2024 -
Genotype_Imputation_hardcall Public
This short script facilitates the conversion of binary genotypes to VCF format, followed by chromosome-specific splitting for subsequent imputation using Minimac4. It then performs a hard-call to s…
UpdatedJun 27, 2024 -
Leveraging the power of LD variational autoencoders to identify latent representations as dim red embeddings of sc data
Jupyter Notebook UpdatedJun 19, 2024 -
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