astrazeneca / skywalkr Goto Github PK

.
├── DESCRIPTION
├── CONTRIBUTING.md
├── LICENSE
├── 🛠️ R --> helper functions for shiny apps
│   ├── server_utils.R
│   └── ui_utils.R
├── README.md
├── renv.lock
├── 💾 data --> necessary input data and sample data files
│   ├── app_data.csv
│   ├── heatmap_data.tsv
│   ├── mtcars.csv
│   ├── nlp_allowed.csv
│   └── sample_data.csv
├── 📄 docs --> within the app documentation
│   ├── intro.md
│   ├── intro_light.md
│   ├── pareto_bar_explained.md
│   ├── pareto_hist_explained.md
│   └── variables_explained.md
├── 🖼️ img --> readme plots
│   ├── skywalkR_interface.png
│   └── skywalkr_light_interface.png
├── 🧬 skywalkR_app.R --> main Shiny app
re-rank CRISPR hits to find promising genes driving drug
resistance in EGFR mutant lung cancer;
└── 🧪 skywalkR_light_app.R --> a demo shiny app,
input any table to test out how multi-objective optimisation works;

@Article{Gogleva2022,
author={Gogleva, Anna
and Polychronopoulos, Dimitris
and Pfeifer, Matthias
and Poroshin, Vladimir
and Ughetto, Micha{\"e}l
and Martin, Matthew J.
and Thorpe, Hannah
and Bornot, Aurelie
and Smith, Paul D.
and Sidders, Ben
and Dry, Jonathan R.
and Ahdesm{\"a}ki, Miika
and McDermott, Ultan
and Papa, Eliseo
and Bulusu, Krishna C.},
title={Knowledge graph-based recommendation framework identifies drivers of resistance in EGFR mutant non-small cell lung cancer},
journal={Nature Communications},
year={2022},
month={Mar},
day={29},
volume={13},
number={1},
pages={1667},
abstract={Resistance to EGFR inhibitors (EGFRi) presents a major obstacle in treating non-small cell lung cancer (NSCLC). One of the most exciting new ways to find potential resistance markers involves running functional genetic screens, such as CRISPR, followed by manual triage of significantly enriched genes. This triage process to identify `high value' hits resulting from the CRISPR screen involves manual curation that requires specialized knowledge and can take even experts several months to comprehensively complete. To find key drivers of resistance faster we build a recommendation system on top of a heterogeneous biomedical knowledge graph integrating pre-clinical, clinical, and literature evidence. The recommender system ranks genes based on trade-offs between diverse types of evidence linking them to potential mechanisms of EGFRi resistance. This unbiased approach identifies 57 resistance markers from >3,000 genes, reducing hit identification time from months to minutes. In addition to reproducing known resistance markers, our method identifies previously unexplored resistance mechanisms that we prospectively validate.},
issn={2041-1723},
doi={10.1038/s41467-022-29292-7},
url={https://doi.org/10.1038/s41467-022-29292-7}
}