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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
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Software . 2024
Data sources: ZENODO
ZENODO
Software . 2024
Data sources: Datacite
ZENODO
Software . 2024
Data sources: Datacite
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Development of an Artificial Neural Network to Identify Immune Cell–Cancer Gene Set Interactions

Authors: Appala, Sreeja;

Development of an Artificial Neural Network to Identify Immune Cell–Cancer Gene Set Interactions

Abstract

Project Description https://github.com/SreejaAppala/ANN-Immune-Cancer Development of an Artificial Neural Network to Identify Immune Cell–Cancer Gene Set Interactions Sreeja Appala 6/27/2024 Code All the code was conducted in Python with TensorFlow sequential class. Artificial Neural Network (ANN) Development First, a general ANN was developed, including all necessary parameters ('1setup.py'). Then, each parameter was tested individually for its optimal value ('2architecture.py' to '9activation.py'). This was done by iterating the model through different values for that parameter while keeping the rest of the model constant. The optimal value was chosen based on the best evaluation metrics from the model within those runs: the lowest MSE, the highest R-squared value, and the highest accuracy. 'finalmodel.py' contains the code for the final artificial neural network (ANN) incorporating all the optimal parameters found earlier. 'output.csv' includes all the predictors and responses that the model trains and validates on, with features being immune cell fractions and targets being gene set enrichment levels. The model achieved an MSE of 0.0035, an R-squared value of 0.99, and an accuracy of 96%. It successfully predicted the relationship between the immune cell fractions and gene set enrichment levels. Later, sensitivity analysis was applied to reveal which immune cells were impacting each of the gene sets. Features and Targets Feature 1 - Memory B cells Feature 2 - Plasma cells Feature 3 - CD4+ T cells Feature 4 - M2 macrophages Feature 5 - Mast cells Feature 6 - Neutrophils Target 1 - Angiogenesis Target 2 - Hedgehog signaling Target 3 - Epithelial–mesenchymal transition (EMT) Target 4 - Apical junction Target 5 - TGF-beta signaling

Keywords

FOS: Computer and information sciences, Artificial intelligence, Bioinformatics

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
0
Average
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Average