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Modeling Dense Multimodal Interactions Between Biological Pathways and Histology for Survival Prediction - CVPR 2024

Python 92.91% Shell 7.09%
histology-transcriptomics mahmoodlab pathology pathology-genomics survpath interpretability pathology-representation pathways

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survpath's Issues

Number of Parameters

Hi,

Thanks for the interesting work. Can you please share the total number of parameters or at least an estimation?
I may have misunderstood it, but I assume that there is a separate SNN block for each pathway. So, If we have 330 pathways here, the pathway tokenizer will have at least 330256256 parameters which is about 21 million. I appreciate your clarification.

Thanks

Discussion on the issue of the basis for the selection of 5-fold cross-validation results and the preservation of trained models.

Thanks for sharing the code, I have a question regarding the experimental setup.1. Is the C-index value under 5-fold cross-validation in the article obtained as the highest C-index value for each fold or the corresponding C-index value when the loss per fold drops to the minimum?2. What criterion are you basing on to save the model for each fold training? Maximum C-index or minimum loss?

the folder structure of dataset

Dear authors,

I found your work on transcriptomics, histology, and multimodal fusion for classification tasks to be quite interesting. I would like to know more about the folder structure you used in your experiments. Specifically, I'm interested in understanding how you organized the different data modalities and their corresponding files.

Could you kindly provide some information or details regarding the folder structure you employed in your study? It would greatly help me in better understanding and replicating your experiments.

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