This library contains functions to build and benchmark a whole-genome perturbative map.
See our bioRxiv paper for details: https://www.biorxiv.org/content/10.1101/2022.12.09.519400v1
Here are the descriptions for the constants used in the code to configure and control various aspects of the map building and benchmarking process:
BENCHMARK_DATA_DIR
: The directory path to the benchmark annotations data. It is obtained using the resources module from the importlib package.
BENCHMARK_SOURCES
: A list of benchmark sources, including "Reactome", "HuMAP", "CORUM", "SIGNOR", and "StringDB".
RECALL_PERC_THRS
: A list of tuples of two floats between 0 and 1 representing the threshold pair (lower threshold, upper threshold) for calculating recall.
RANDOM_SEED
: The random seed value used for random number generation for sampling the null distribution.
N_NULL_SAMPLES
: The number of null samples used in benchmarking.
MIN_REQ_ENT_CNT
: The minimum required number of entities for benchmarking.
Besides above parameters, for each map we build, we utilize distinct constants to indicate the metadata columns for the perturbation, control, and batch information.
This package is installable via pip
.
pip install efaar_benchmarking
First, run notebooks/map_building_benchmarking.ipynb
for GWPS, cpg0016, and cpg0021 individually. This process will build each of these maps and report the perturbation signal and biological relationship benchmarks. Afterwards, run notebooks/map_evaluation_comparison.ipynb
to explore the constructed maps using the methods presented in our paper. In order for the latter notebook to work, make sure to set the save_results
parameter to True in the former notebook.
We've uploaded the 128-dimensional PCA-TVN maps we constructed for GWPS, cpg0016, and cpg0021 to the notebooks/data
directory. So, for convenience, one can run notebooks/map_evaluation_comparison.ipynb
directly on these uploaded map files if they wish to explore the maps further without running notebooks/map_building_benchmarking.ipynb
. See notebooks/data/LICENSE
for terms of use for each dataset.
RxRx3 embeddings are available as separate parquet files per plate in the embeddings.tar file, downloadable from https://rxrx3.rxrx.ai/downloads. Note that in this data, all but 733 genes are anonymized.
You have to install GitHub LFS (Large File Storage) to properly utilize the files under notebooks/data
and efaar_benchmarking/expression_data
in your local clone of the repository.
See CONTRIBUTING.md
for code contribution guidance.
If you want to add any new annotation sources, make sure to follow the same format as in the benchmark_annotations
folder. Your annotations file needs to be a file with a .txt
extension. It is expected to be a comma-separated two column data frame where column names are entity1
and entity2
.
See efaar_benchmarking/benchmark_annotations/LICENSE
for terms of use for each source.
Reactome:
Gillespie, M., Jassal, B., Stephan, R., Milacic, M., Rothfels, K., Senff-Ribeiro, A., Griss, J., Sevilla, C., Matthews, L., Gong, C., et al. (2022). The reactome pathway knowledgebase 2022. Nucleic Acids Res. 50, D687–D692. 10.1093/nar/gkab1028.
CORUM:
Giurgiu, M., Reinhard, J., Brauner, B., Dunger-Kaltenbach, I., Fobo, G., Frishman, G., Montrone, C., and Ruepp, A. (2019). CORUM: the comprehensive resource of mammalian protein complexes-2019. Nucleic Acids Res. 47, D559–D563. 10.1093/nar/gky973.
HuMAP:
Drew, K., Wallingford, J.B., and Marcotte, E.M. (2021). hu.MAP 2.0: integration of over 15,000 proteomic experiments builds a global compendium of human multiprotein assemblies. Mol. Syst. Biol. 17, e10016. 10.15252/msb.202010016.
SIGNOR:
Licata, L., Lo Surdo, P., Iannuccelli, M., Palma, A., Micarelli, E., Perfetto, L., Peluso, D., Calderone, A., Castagnoli, L., and Cesareni, G. (2019). SIGNOR 2.0, the SIGnaling Network Open Resource 2.0: 2019 update. Nucleic Acids Research. 10.1093/nar/gkz949.
StringDB:
von Mering C, Jensen LJ, Snel B, Hooper SD, Krupp M, Foglierini M, Jouffre N, Huynen MA, Bork P. STRING: known and predicted protein-protein associations, integrated and transferred across organisms. Nucleic Acids Res. 2005 Jan 1;33(Database issue):D433-7. doi: 10.1093/nar/gki005.