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Search the biomedical literature for protein interactions andprotein associations.

Project description

PEDL

PEDL is a tool for predicting protein-protein assocations from the biomedical literature. It searches more than 30 million abstracts of biomedical publications and over 4 million full texts with the help of PubTatorCentral. A state-of-the-art machine reading model then predicts which types of association between the proteins are supported by the literature. Among others, PEDL can detect posttranslational modifications, transcription factor-target interactions, complex formations and controlled transports.

Installation

pip install pedl

Usage

PEDL supports two commands pedl predict and pedl summarize. The default workflow is to first predict associations for one or more protein pairs of interest, which will store the results for each pair in a separate file. The contents of these files can then be aggregated into a single csv-file with summarize.

PEDL expects proteins to be identified via entrez gene ids. These can be looked up via standard webinterfaces like NCBI Gene.

predict

  • Interactions between single proteins

    pedl predict --p1 29126 --p2 54918 --out PEDL_predictions
    

    Results:

    $ ls PEDL_predictions/
    CD274-CMTM6.txt  CMTM6-CD274.txt
    
    $ head -n1 PEDL_predictions/CD274-CMTM6.txt
    in-complex-with	0.98	6978769	A PD-L1 antibody, H1A, was developed to destabilize PD-L1 by disrupting the <e1>PD-L1</e1> stabilizer <e2>CMTM6</e2>.	PEDL
    
  • Pairwise interactions between multiple proteins

    pedl predict --p1 29126 --p2  54918 920  --out PEDL_predictions
    

    searches for interactions between 29126 and 54918, and for interactions between 29126 and 920

  • Read protein lists from files

    pedl predict --p1 proteins.txt --p2  54918 920  --out PEDL_predictions
    

    searches for interactions between the proteins in proteins.txt and 54918, as well as interactions between proteins in proteins.txt and 920

  • Search for multiple species at once

    If the provided gene ids are from human, mouse, rat or zebrafish, PEDL can automatically search for interactions in the other model species (currently human, mouse, rat and zebrafish) via homology classes defined by the Alliance of Genome Resources:

    pedl predict --p1 29126 --p2 54918 --out PEDL_predictions --expand_species mouse zebrafish
    

    would also include interactions in mouse and zebrafish.

  • Interactions from pathway databases

    It is also possible to query PathwayCommons for interactions. This requires the python package indra to be installed, which can be achieved via pip install indra:

      pedl predict --p1 29126 --p2 54918 --out PEDL_predictions --dbs pid reactome kegg
    

    to query pid reactome and kegg. See --help for the full list of available databases.

  • Large gene lists

    If you need to test for more than 100 interactions at once, you have to use a local copy of PubTatorCentral, which can be downloaded here. Unpack the PubTatorCentral files and point PEDL towards the files:

    pedl predict --p1 large_protein_list1.txt --p2 large_protein_list2 --out PEDL_predictions --pubtator [PATH_TO_PUBTATOR]
    

    In this case, it is also strongly advised to use a CUDA-compatible GPU to speed up the machine reading:

    pedl predict --p1 large_protein_list1.txt --p2 large_protein_list2 --out PEDL_predictions
      --pubtator [PATH_TO_PUBTATOR]--device cuda
    

summarize

pedl summarize PEDL_predictions [--out PATH_TO_SUMMARY_CSV]
  • By default, PEDL will create the summary CSV in the directory containing PEDL_predictions

References

Code and instructions to reproduce the results of our paper, can be found here.

If you use PEDL in your work, please cite us

@article{weber2020pedl,
  title={PEDL: extracting protein--protein associations using deep language models and distant supervision},
  author={Weber, Leon and Thobe, Kirsten and Migueles Lozano, Oscar Arturo and Wolf, Jana and Leser, Ulf},
  journal={Bioinformatics},
  volume={36},
  number={Supplement\_1},
  pages={i490--i498},
  year={2020},
  publisher={Oxford University Press}
}

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