Metadata-Version: 2.1
Name: deepac
Version: 0.14.0
Summary: Predicting pathogenic potentials of novel DNA with reverse-complement neural networks.
Home-page: https://gitlab.com/rki_bioinformatics/DeePaC
Author: Jakub Bartoszewicz
Author-email: jakub.bartoszewicz@hpi.de
License: MIT
Description: <!-- {#mainpage} -->
        
        # DeePaC
        
        DeePaC is a python package and a CLI tool for predicting labels (e.g. pathogenic potentials) from short DNA sequences (e.g. Illumina 
        reads) with interpretable reverse-complement neural networks. For details, see our preprint on bioRxiv: 
        <https://www.biorxiv.org/content/10.1101/535286v3> and the paper in *Bioinformatics*: <https://doi.org/10.1093/bioinformatics/btz541>.
        For details regarding the interpretability functionalities of DeePaC, see the preprint here: <https://www.biorxiv.org/content/10.1101/2020.01.29.925354v2>
        
        Documentation can be found here:
        <https://rki_bioinformatics.gitlab.io/DeePaC/>. 
        See also the main repo here: <https://gitlab.com/rki_bioinformatics/DeePaC>.
        
        ## Plug-ins
        ### DeePaC-strain
        Basic version of DeePaC comes with built-in models trained to predict pathogenic potentials of NGS reads originating from
        novel *bacteral species*. If you want to predict pathogenicity of novel *strains* of *known* species, try the DeePaC-strain plugin available here:
        <https://gitlab.com/dacs-hpi/DeePaC-strain>. 
        
        ### DeePaC-vir
        If you want to detect novel human viruses, try the DeePaC-vir plugin: <https://gitlab.com/dacs-hpi/DeePaC-vir>. 
        
        ### DeePaC-Live
        If you want to run the predictions in real-time during an Illumina sequencing run, try DeePaC-Live: <https://gitlab.com/dacs-hpi/deepac-live>. 
        
        
        ## Installation
        
        We recommend using Bioconda (based on the `conda` package manager) or custom Docker images based on official Tensorflow images.
        Alternatively, a `pip` installation is possible as well. For installation on IBM Power Systems (e.g. AC992), see separate [installation instructions (experimental)](https://gitlab.com/rki_bioinformatics/DeePaC/-/blob/master/dockerfiles/ppc64le/README.md).
        
        ### With Bioconda (recommended)
         [![install with bioconda](https://img.shields.io/badge/install%20with-bioconda-brightgreen.svg?style=flat)](http://bioconda.github.io/recipes/deepac/README.html)
         
        You can install DeePaC with `bioconda`. Set up the [bioconda channel](
        <https://bioconda.github.io/user/install.html#set-up-channels>) first (channel ordering is important):
        
        ```
        conda config --add channels defaults
        conda config --add channels bioconda
        conda config --add channels conda-forge
        ```
        
        We recommend setting up an isolated `conda` environment:
        ```
        # python 3.6, 3.7 and 3.8 are supported
        conda create -n my_env python=3.8
        conda activate my_env
        ```
        
        and then:
        ```
        # For GPU support (recommended)
        conda install tensorflow-gpu deepac
        # Basic installation (CPU-only)
        conda install deepac
        ```
        
        Optional: download and compile the latest deepac-live custom models [![DOI](https://zenodo.org/badge/DOI/10.5281/zenodo.4456008.svg)](https://doi.org/10.5281/zenodo.4456008):
        ```
        deepac getmodels --fetch
        ```
        
        If you want to install the plugins as well, use:
        
        ```
        conda install deepacvir deepacstrain
        ```
        
        ### With Docker (also recommended)
        
        Requirements: 
        * install [Docker](https://docs.docker.com/get-docker/) on your host machine. 
        * For GPU support, you have to install the [NVIDIA Docker support](https://github.com/NVIDIA/nvidia-docker) as well.
        
        See [TF Docker installation guide](https://www.tensorflow.org/install/docker) and the 
        [NVIDIA Docker support installation guide](https://docs.nvidia.com/datacenter/cloud-native/container-toolkit/install-guide.html#docker) 
        for details. The guide below assumes you have Docker 19.03 or above.
        
        You can then pull the desired image:
        ```
        # Basic installation - CPU only
        docker pull dacshpi/deepac:0.13.5
        
        # For GPU support
        docker pull dacshpi/deepac:0.13.5-gpu
        ```
        
        And run it:
        ```
        # Basic installation - CPU only
        docker run -v $(pwd):/deepac -u $(id -u):$(id -g) --rm dacshpi/deepac:0.13.5 deepac --help
        docker run -v $(pwd):/deepac -u $(id -u):$(id -g) --rm dacshpi/deepac:0.13.5 deepac test -q
        
        # With GPU support
        docker run -v $(pwd):/deepac -u $(id -u):$(id -g) --rm --gpus all dacshpi/deepac:0.13.5-gpu deepac test
        
        # If you want to use the shell inside the container
        docker run -it -v $(pwd):/deepac -u $(id -u):$(id -g) --rm --gpus all dacshpi/deepac:0.13.5-gpu bash
        ```
        
        The image ships the main `deepac` package along with the `deepac-vir` and `deepac-strain` plugins. See the basic usage guide below for more deepac commands.
        
        Optional: download and compile the latest deepac-live custom models [![DOI](https://zenodo.org/badge/DOI/10.5281/zenodo.4456008.svg)](https://doi.org/10.5281/zenodo.4456008):
        ```
        docker run -v $(pwd):/deepac -u $(id -u):$(id -g) --rm --gpus all dacshpi/deepac:0.13.5 deepac --fetch
        ```
        
        For more information about the usage of the NVIDIA container toolkit (e.g. selecting the GPUs to use),
         consult the [User Guide](https://docs.nvidia.com/datacenter/cloud-native/container-toolkit/user-guide.html#user-guide).
        
        The `dacshpi/deepac:latest` corresponds to the latest version of the CPU build. We recommend using explicit version tags instead.
        
        ### With pip
        
        We recommend setting up an isolated `conda` environment (see above). Alternatively, you can use a `virtualenv` virtual environment (note that deepac requires python 3):
        ```
        # use -p to use the desired python interpreter (python 3.6 or higher required)
        virtualenv -p /usr/bin/python3 my_env
        source my_env/bin/activate
        ```
        
        You can then install DeePaC with `pip`. For GPU support, you need to install CUDA and CuDNN manually first (see TensorFlow installation guide for details). 
        Then you can do the same as above:
        
        ```
        pip install deepac
        ```
        
        Optional: download and compile the latest deepac-live custom models [![DOI](https://zenodo.org/badge/DOI/10.5281/zenodo.4456008.svg)](https://doi.org/10.5281/zenodo.4456008):
        ```
        deepac getmodels --fetch
        ```
        
        If you want to install the plugins, use:
        
        ```
        pip install deepacvir deepacstrain
        ```
        
        ### Optional: run tests
        Optionally, you can run explicit tests of your installation. Note that it may take some time on a CPU.
        ```
        # Run standard tests
        deepac test
        # Run quick tests (eg. on CPUs)
        deepac test -q
        # Test using specific GPUs (here: /device:GPU:0 and /device:GPU:1) 
        deepac test -g 0 1
        # Test explainability and gwpa workflows
        deepac test -xp
        # Full tests
        deepac test -a
        # Full quick tests (eg. on GPUs with limited memory)
        deepac test -aq
        ```
        
        ### Help
        
        To see help, just use
        ```
        deepac --help
        deepac predict --help
        deepac train --help
        # Etc.
        ```
        
        ## Basic use: prediction
        
        You can predict pathogenic potentials with one of the built-in models out of the box:
        ```
        # A rapid CNN (trained on IMG/M data)
        deepac predict -r input.fasta
        # A sensitive LSTM (trained on IMG/M data)
        deepac predict -s input.fasta
        ```
        
        The rapid and the sensitive models are trained to predict pathogenic potentials of novel bacterial species.
        For details, see <https://doi.org/10.1093/bioinformatics/btz541> or <https://www.biorxiv.org/content/10.1101/535286v3>.
        
        To quickly filter your data according to predicted pathogenic potentials, you can use:
        ```
        deepac predict -r input.fasta
        deepac filter input.fasta input_predictions.npy -t 0.5
        ```
        Note that after running `predict`, you can use the `input_predictions.npy` to filter your fasta file with different
        thresholds. You can also add pathogenic potentials to the fasta headers in the output files:
        ```
        deepac filter input.fasta input_predictions.npy -t 0.75 -p -o output-75.fasta
        deepac filter input.fasta input_predictions.npy -t 0.9 -p -o output-90.fasta
        ```
        
        ## Advanced use
        ### Config templates
        To get the config templates in the current working directory, simply use:
        ```
        deepac templates
        ```
        ### Preprocessing
        
        For more complex analyzes, it can be useful to preprocess the fasta files by converting them to binary numpy arrays. Use:
        ```
        deepac preproc preproc_config.ini
        ```
        See the `config_templates` directory of the GitLab repository (https://gitlab.com/rki_bioinformatics/DeePaC/) for a sample configuration file.
        
        ### Training
        You can use the built-in architectures to train a new model:
        ```
        deepac train -r -T train_data.npy -t train_labels.npy -V val_data.npy -v val_labels.npy
        deepac train -s -T train_data.npy -t train_labels.npy -V val_data.npy -v val_labels.npy
        
        ```
        
        To train a new model based on you custom configuration, use
        ```
        deepac train -c nn_train_config.ini
        ```
        
        If you train an LSTM on a GPU, a CUDNNLSTM implementation will be used. To convert the resulting model to be 
        CPU-compatible, use `deepac convert`. You can also use it to save the weights of a model, or recompile a model 
        from a set of weights:
        
        ```
        # Save model weights and convert the model to an equivalent with the same architecture and weights.
        # Other config parameters can be adjusted
        deepac convert model_config.ini saved_model.h5
        # Recompile the model
        deepac convert saved_model_config.ini saved_model_weights.h5 -w
        ```
        
        ### Evaluation
        
        To evaluate a trained model, use
        ```
        # Read-by-read performance
        deepac eval -r eval_config.ini
        # Species-by-species performance
        deepac eval -s eval_species_config.ini
        # Ensemble performance
        deepac eval -e eval_ens_config.ini
        ```
        See the configs directory for sample configuration files. Note that `deepac eval -s` requires precomputed predictions 
        and a csv file with a number of DNA reads for each species in each of the classes.
        
        ### TPU (experimental)
        If you want to use a TPU, run DeePaC with the `--tpu` parameter:
        ```
        # Test a TPU
        deepac --tpu colab test
        ```
        
        ## Intepretability workflows
        ### Filter visualization
        To find the most relevant filters and visualize them, use the following minimum workflow: 
        ```
        # Calculate filter and nucleotide contibutions (partial Shapley values) for the first convolutional layer
        # using mean-centered weight matrices and "easy" calculation mode
        deepac explain fcontribs -m model.h5 -eb -t test_data.npy -N test_nonpatho.fasta -P test_patho.fasta -o fcontribs 
        
        # Create filter ranking
        deepac explain franking -f fcontribs/filter_scores -y test_labels.npy -p test_predictions.npy -o franking
        
        # Prepare transfac files for filter visualization (weighted by filter contribution)
        deepac explain fa2transfac -i fcontribs/fasta -o fcontribs/transfac -w -W fcontribs/filter_scores
        
        # Visualize nucleotide contribution sequence logos
        deepac explain xlogos -i fcontribs/fasta -s fcontribs/nuc_scores -I fcontribs/transfac -t train_data.npy -o xlogos
        ```
        You can browse through other supplementary functionalities and parameters by checking the help:
        ```
        deepac explain -h
        deepac explain fcontribs -h
        deepac explain xlogos -h
        # etc.
        ```
        
        ### Genome-wide phenotype potential analysis (GWPA)
        To find interesting regions of a whole genome, use this workflow to generate nucleotide-resolution maps of
        predicted phenotype potentials and nucleotide contributions:
        ```
        # Fragment the genomes into pseudoreads
        deepac gwpa fragment -g genomes_fasta -o fragmented_genomes
        
        # Predict the pathogenic potential of each pseudoread
        deepac predict -r -a fragmented_genomes/sample1_fragmented_genomes.npy -o predictions/sample1_pred.npy
        
        # Create bedgraphs of mean pathogenic potential at each position of the genome
        # Can be visualized in IGV
        deepac gwpa genomemap -f fragmented_genomes -p predictions -g genomes_genome -o bedgraph
        
        # Rank genes by mean pathogenic potential
        deepac gwpa granking -p bedgraph -g genomes_gff -o granking
        
        # Create bedgraphs of mean nuclotide contribution at each position of the genome
        # Can be visualized in IGV
        deepac gwpa ntcontribs -m model.h5 -f fragmented_genomes -g genomes_genome -o bedgraph_nt
        ```
        You can browse through other supplementary functionalities and parameters by checking the help:
        ```
        deepac gwpa -h
        deepac gwpa genomemap -h
        deepac gwpa ntcontribs -h
        # etc.
        ```
        ### Filter enrichment analysis
        Finally, you can check for filter enrichment in annotated genes or other genomic features:
        ```
        # Get filter activations, genome-wide
        deepac gwpa factiv -m model.h5 -t fragmented_genomes/sample1_fragmented_genomes.npy -f fragmented_genomes/sample1_fragmented_genomes.fasta -o factiv
        
        # Check for enrichment within annotated genomic features
        deepac gwpa fenrichment -i factiv -g genomes_gff/sample1.gff -o fenrichment
        ```
        
        ## Supplementary data and scripts
        Datasets are available here: [![DOI](https://zenodo.org/badge/DOI/10.5281/zenodo.3678563.svg)](https://doi.org/10.5281/zenodo.3678563) (bacteria) and here: [![DOI](https://zenodo.org/badge/DOI/10.5281/zenodo.4312525.svg)](https://doi.org/10.5281/zenodo.4312525) (viruses).
        In the supplement_paper directory you can find the R scripts and data files used in the papers for dataset preprocessing and benchmarking.
        
        ## Erratum
        The second sentence in section 2.2.3 of the bacterial DeePaC paper (<https://doi.org/10.1093/bioinformatics/btz541>) is partially incomplete.
        
        Published text: “All were initialized with He weight initialization (He et al, 2015) and trained…”
        
        Should be: “All were initialized with He weight initialization (He et al, 2015) or Glorot initialization (Glorot & Bengio, 2010) for recurrent and feedforward layers respectively and trained…
        
        ## Known issues
        Unfortunately, the following issues are independent of the DeePaC codebase:
        * pip installation of pybedtools (a deepac dependency) requires libz-dev and will fail if it is not present on your system. To solve this, install libz-dev or use the bioconda installation.
        * A bug in TF 2.2 may cause training to hang when using Keras Sequence input (i.e. if your training config contains
         `Use_TFData = False` and `LoadTrainingByBatch = True`). To solve this, use TF 2.1 or TF 2.3+,
          pre-load your data into memory (`LoadTrainingByBatch = False`) or use TFDataset input (`Use_TFData = True`).
        * A bug in TF 2.1 resets the optimizer state when continuing interrupted training. DeePaC will notice that and warn you, but to solve this, upgrade to TF 2.2+.
        * h5py>=3.0 is not compatible with Tensorflow at the moment and will cause errors when loading Keras (and DeePaC) models (hence, deepac tests will fail as well). 
        Conda installation takes care of it automatically, but the pip Tensorflow installation does not. To solve it, use conda installation or install h5py<3.0. 
        This issue should be resolved in a future version of Tensorflow.
        * shap 0.38 requires IPython but the pip installer does not install it. Manual installation solves the problem.
        
        ## Cite us
        If you find DeePaC useful, please cite:
        
        ```
        @article{10.1093/bioinformatics/btz541,
            author = {Bartoszewicz, Jakub M and Seidel, Anja and Rentzsch, Robert and Renard, Bernhard Y},
            title = "{DeePaC: predicting pathogenic potential of novel DNA with reverse-complement neural networks}",
            journal = {Bioinformatics},
            year = {2019},
            month = {07},
            issn = {1367-4803},
            doi = {10.1093/bioinformatics/btz541},
            url = {https://doi.org/10.1093/bioinformatics/btz541},
            eprint = {http://oup.prod.sis.lan/bioinformatics/advance-article-pdf/doi/10.1093/bioinformatics/btz541/28971344/btz541.pdf},
        }
        
        @article {Bartoszewicz2020.01.29.925354,
            author = {Bartoszewicz, Jakub M. and Seidel, Anja and Renard, Bernhard Y.},
            title = {Interpretable detection of novel human viruses from genome sequencing data},
            elocation-id = {2020.01.29.925354},
            year = {2020},
            doi = {10.1101/2020.01.29.925354},
            publisher = {Cold Spring Harbor Laboratory},
            URL = {https://www.biorxiv.org/content/early/2020/02/01/2020.01.29.925354},
            eprint = {https://www.biorxiv.org/content/early/2020/02/01/2020.01.29.925354.full.pdf},
            journal = {bioRxiv}
        }
        
        ```
Keywords: deep learning DNA sequencing synthetic biology pathogenicity prediction
Platform: UNKNOWN
Classifier: Development Status :: 4 - Beta
Classifier: License :: OSI Approved :: MIT License
Classifier: Programming Language :: Python :: 3
Classifier: Programming Language :: Python :: 3.6
Classifier: Programming Language :: Python :: 3.7
Classifier: Programming Language :: Python :: 3.8
Classifier: Topic :: Scientific/Engineering :: Bio-Informatics
Requires-Python: >=3
Description-Content-Type: text/markdown
