flexynesis 0.2.13

A deep-learning based multi-omics bulk sequencing data integration suite with a focus on (pre-)clinical endpoint prediction.

flexynesis

A deep-learning based multi-omics bulk sequencing data integration suite with a focus on (pre-)clinical endpoint prediction. The package includes multiple types of deep learning architectures such as simple fully connected networks, supervised variational autoencoders, graph convolutional networks, multi-triplet networks different options of data layer fusion, and automates feature selection and hyperparameter optimisation. The tools are continuosly benchmarked on publicly available datasets mostly related to the study of cancer. Some of the applications of the methods we develop are drug response modeling in cancer patients or preclinical models (such as cell lines and patient-derived xenografts), cancer subtype prediction, or any other clinically relevant outcome prediction that can be formulated as a regression, classification, survival, or cross-modality prediction problem.

Citing our work

In order to refer to our work, please cite our manuscript currently available at BioRxiv.

Getting started with Flexynesis

Command-line tutorial

• Getting Started with Flexynesis

Jupyter notebooks for interactive usage

• Modeling Breast Cancer Subtypes
• Survival Markers of Lower Grade Gliomas
• Unsupervised Analysis of Bone Marrow Cells

Benchmarks

For the latest benchmark results see: https://bimsbstatic.mdc-berlin.de/akalin/buyar/flexynesis-benchmark-datasets/dashboard.html

The code for the benchmarking pipeline is at: https://github.com/BIMSBbioinfo/flexynesis-benchmarks

Documentation

Documentation generated using mkdocs

pip install mkdocstrings[python]
mkdocs build --clean