--- a/README.md
+++ b/README.md
@@ -1,114 +1,114 @@
-# MOVE (Multi-Omics Variational autoEncoder)
-
-[![PyPI version](https://badge.fury.io/py/move-dl.svg)](https://badge.fury.io/py/move-dl)
-[![Documentation Status](https://readthedocs.org/projects/move-dl/badge/?version=latest)](https://move-dl.readthedocs.io/?badge=latest)
-
-The code in this repository can be used to run our Multi-Omics Variational
-autoEncoder (MOVE) framework for integration of omics and clinical variabels
-spanning both categorial and continuous data. Our approach includes training
-ensemble VAE models and using *in silico* perturbation experiments to identify
-cross omics associations. The manuscript has been published in Nature
-Biotechnology:
-
-> Allesøe, R.L., Lundgaard, A.T., Hernández Medina, R. *et al*. Discovery of
-> drug–omics associations in type 2 diabetes with generative deep-learning
-> models. *Nat Biotechnol* (2023). https://doi.org/10.1038/s41587-022-01520-x
-
-We developed the method based on a Type 2 Diabetes cohort from the IMI DIRECT
-project containing 789 newly diagnosed T2D patients. The cohort and data
-creation is described in
-[Koivula et al.](https://dx.doi.org/10.1007%2Fs00125-019-4906-1) and
-[Wesolowska-Andersen et al.](https://doi.org/10.1016/j.xcrm.2021.100477). For
-the analysis we included the following data:
-
-Multi-omics data sets:
-```
-Genomics
-Transcriptomics
-Proteomics
-Metabolomics
-Metagenomics
-```
-
-Other data sets:
-```
-Clinical data (blood measurements, imaging data, ...)
-Questionnaire data (diet etc)
-Accelerometer data
-Medication data
-```
-
-# Installation
-
-## Installing MOVE package
-
-MOVE is written in Python and can be installed using `pip`:
-
-```bash
->>> pip install move-dl
-```
-
-## Requirements
-
-MOVE should run on any environmnet where Python is available. The variational
-autoencoder architecture is implemented in PyTorch.
-
-The training of the VAEs can be done using CPUs only or GPU acceleration. If
-you do not have powerful GPUs available, it is possible to run using only CPUs.
-For instance, the tutorial data set consisting of simulated drug, metabolomics
-and proteomics data for 500 individuals runs fine on a standard macbook.
-
-> Note: The pip installation of `move-dl` does not setup your local GPU automatically
-
-# The MOVE pipeline
-
-MOVE has five-six steps:
-
-```
-01. Encode the data into a format that can be read by MOVE
-02. Finding the right architecture of the network focusing on reconstruction accuracy
-03. Finding the right architecture of the network focusing on stability of the model
-04. Use model, determined from steps 02-03, to create and analyze the latent space
-05. Identify associations between a categorical and continuous datasets
-05a. Using an ensemble of VAEs with the t-test approach
-05b. Using an ensemble of VAEs with the Bayesian decision theory approach
-06. If both 5a and 5b were run select the overlap between them
-```
-
-## How to run MOVE
-
-Please refer to our [**documentation**](https://move-dl.readthedocs.io/) for
-examples and [tutorials](https://move-dl.readthedocs.io/tutorial/index.html)
-on how to run MOVE.
-
-Additionally, you can copy
-[this notebook](https://colab.research.google.com/drive/1RFWNsuGymCmppPsElBvDuA9zRbGskKmi?usp=sharing)
-and follow its instructions to get familiar with our pipeline.
-
-# Data sets
-
-## DIRECT data set
-
-The data used in notebooks are not available for testing due to the informed
-consent given by study participants, the various national ethical approvals for
-the study, and the European General Data Protection Regulation (GDPR).
-Therefore, individual-level clinical and omics data cannot be transferred from
-the centralized IMI-DIRECT repository. Requests for access to summary statistics
-IMI-DIRECT data, including those presented here, can be made to
-DIRECTdataaccess@Dundee.ac.uk. Requesters will be informed on how summary-level
-data can be accessed via the DIRECT secure analysis platform following
-submission of appropriate application. The IMI-DIRECT data access policy is
-available [here](https://directdiabetes.org).
-
-## Simulated and publicaly available data sets
-
-We have therefore provided two datasets to test the workflow: a simulated
-dataset and a publicly-available maize rhizosphere microbiome data set.
-
-# Citation
-
-To cite MOVE, use the following information:
-
-Allesøe, R.L., Lundgaard, A.T., Hernández Medina, R. *et al*. Discovery of
-drug–omics associations in type 2 diabetes with generative deep-learning models.
-*Nat Biotechnol* (2023). https://doi.org/10.1038/s41587-022-01520-x
+# MOVE (Multi-Omics Variational autoEncoder)
+
+[![PyPI version](https://badge.fury.io/py/move-dl.svg)](https://badge.fury.io/py/move-dl)
+[![Documentation Status](https://readthedocs.org/projects/move-dl/badge/?version=latest)](https://move-dl.readthedocs.io/?badge=latest)
+
+The code in this repository can be used to run our Multi-Omics Variational
+autoEncoder (MOVE) framework for integration of omics and clinical variabels
+spanning both categorial and continuous data. Our approach includes training
+ensemble VAE models and using *in silico* perturbation experiments to identify
+cross omics associations. The manuscript has been published in Nature
+Biotechnology:
+
+Allesøe, R.L., Lundgaard, A.T., Hernández Medina, R. *et al*. Discovery of
+drug–omics associations in type 2 diabetes with generative deep-learning
+models. *Nat Biotechnol* (2023). https://doi.org/10.1038/s41587-022-01520-x
+
+We developed the method based on a Type 2 Diabetes cohort from the IMI DIRECT
+project containing 789 newly diagnosed T2D patients. The cohort and data
+creation is described in
+[Koivula et al.](https://dx.doi.org/10.1007%2Fs00125-019-4906-1) and
+[Wesolowska-Andersen et al.](https://doi.org/10.1016/j.xcrm.2021.100477). For
+the analysis we included the following data:
+
+Multi-omics data sets:
+```
+Genomics
+Transcriptomics
+Proteomics
+Metabolomics
+Metagenomics
+```
+
+Other data sets:
+```
+Clinical data (blood measurements, imaging data, ...)
+Questionnaire data (diet etc)
+Accelerometer data
+Medication data
+```
+
+# Installation
+
+## Installing MOVE package
+
+MOVE is written in Python and can be installed using `pip`:
+
+```bash
+>>> pip install move-dl
+```
+
+## Requirements
+
+MOVE should run on any environmnet where Python is available. The variational
+autoencoder architecture is implemented in PyTorch.
+
+The training of the VAEs can be done using CPUs only or GPU acceleration. If
+you do not have powerful GPUs available, it is possible to run using only CPUs.
+For instance, the tutorial data set consisting of simulated drug, metabolomics
+and proteomics data for 500 individuals runs fine on a standard macbook.
+
+ Note: The pip installation of `move-dl` does not setup your local GPU automatically
+
+# The MOVE pipeline
+
+MOVE has five-six steps:
+
+```
+01. Encode the data into a format that can be read by MOVE
+02. Finding the right architecture of the network focusing on reconstruction accuracy
+03. Finding the right architecture of the network focusing on stability of the model
+04. Use model, determined from steps 02-03, to create and analyze the latent space
+05. Identify associations between a categorical and continuous datasets
+05a. Using an ensemble of VAEs with the t-test approach
+05b. Using an ensemble of VAEs with the Bayesian decision theory approach
+06. If both 5a and 5b were run select the overlap between them
+```
+
+## How to run MOVE
+
+Please refer to our [**documentation**](https://move-dl.readthedocs.io/) for
+examples and [tutorials](https://move-dl.readthedocs.io/tutorial/index.html)
+on how to run MOVE.
+
+Additionally, you can copy
+[this notebook](https://colab.research.google.com/drive/1RFWNsuGymCmppPsElBvDuA9zRbGskKmi?usp=sharing)
+and follow its instructions to get familiar with our pipeline.
+
+# Data sets
+
+## DIRECT data set
+
+The data used in notebooks are not available for testing due to the informed
+consent given by study participants, the various national ethical approvals for
+the study, and the European General Data Protection Regulation (GDPR).
+Therefore, individual-level clinical and omics data cannot be transferred from
+the centralized IMI-DIRECT repository. Requests for access to summary statistics
+IMI-DIRECT data, including those presented here, can be made to
+DIRECTdataaccess@Dundee.ac.uk. Requesters will be informed on how summary-level
+data can be accessed via the DIRECT secure analysis platform following
+submission of appropriate application. The IMI-DIRECT data access policy is
+available [here](https://directdiabetes.org).
+
+## Simulated and publicaly available data sets
+
+We have therefore provided two datasets to test the workflow: a simulated
+dataset and a publicly-available maize rhizosphere microbiome data set.
+
+# Citation
+
+To cite MOVE, use the following information:
+
+Allesøe, R.L., Lundgaard, A.T., Hernández Medina, R. *et al*. Discovery of
+drug–omics associations in type 2 diabetes with generative deep-learning models.
+*Nat Biotechnol* (2023). https://doi.org/10.1038/s41587-022-01520-x