Welcome to the GitHub repository "Nephro Candidate Score". The Nephro Candidate Score (NCS) is a tool for standardized and automatic prioritization of candidate variants in kidney disease patients. It integrates information from multiple open-source databases and scores variants based on a machine learning algorithm.
TODO
The NCS is publicly available and accessible. A web tool version for single variant scoring is available on TBA. A command line tool for scoring .vcf files is available on TBA.
The repository has the following structure:
.
├── gene_score/
│ ├── features/
│ │ ├── raw/
│ │ ├── results/
│ │ ├── scripts/
│ │ │ ├── cellxgene.R
│ │ │ ├── descartes.R
│ │ │ ├── exon_CpG_o2e_ratio.R
│ │ │ ├── exon_and_prom_conservation.R
│ │ │ ├── gnomad.R
│ │ │ ├── gtex.R
│ │ │ ├── kidney_network.R
│ │ │ ├── mgi_mpo.R
│ │ │ ├── nephrogenesis_atlas.R
│ │ │ ├── paralogues.R
│ │ │ ├── promoter_CpG_o2e_ratio.R
│ │ ├── helper_functions.R
│ ├── labels/
│ │ ├── raw/
│ │ ├── results/
│ │ ├── scripts/
│ │ │ ├── dispensable_genes.R
│ │ │ ├── positive_genes.R
│ ├── raw/
│ ├── training/
│ ├── gene_score_preprocessing_master.R
│ ├── helper_functions.R
│ ├── hgnc_functions.R
└── variant_score/
- The
gene_score/
directory contains all scripts relevant for data acquisition and machine learning development of the gene score. Due to large file sizes, the raw data is not completely stored on GitHub. - The
variant_score/
TBA
This project is licensed under the terms of the MIT license. For more information, please refer to the License TBA file.
Nina Rank
Bernt Popp
- https://twitter.com/berntpopp
- https://github.com/berntpopp
- https://orcid.org/0000-0002-3679-1081
- https://scholar.google.com/citations?user=Uvhu3t0AAAAJ
Soeren Lukassen
- https://github.com/slukassen
- https://orcid.org/0000-0001-7045-6327
- https://scholar.google.com/citations?user=wWiHGZkAAAAJ&hl=en
Constantin Aaron Wolff
Jan Halbritter
If you have any questions, suggestions, or feedback, please feel free to contact [email protected].