binary classification model of supervised cnn deep learning with multiple hidden layers Search Results


90
Panoptes Pharma GmbH multi-resolution cnn architecture
Workflow and Panoptes architecture (A) A total of 456 patients in the cohorts from CPTAC and TCGA with feature annotations. (B) Overall workflow. I, H&E slide images of endometrial cancers were downloaded from databases; II, slides were separated at the per-patient level into a training, validation, and test set; III, slides were cut into 299 × 299-pixel tiles excluding background, and contaminants and qualified tiles were packaged into TFrecord files for each set; IV, training and validation sets were used to train the convolutional neural networks, and the testing set was used to evaluate trained models; V, activation maps of test set tiles were extracted and dimensionally reduced by tSNE to visualize features, while the per-tile predictions were aggregated back into intact slides; VI, an independent test set with samples from NYU hospitals was used to test the generalizability of selected best-performing models. (C) Slides were cut into paired tile sets at 2.5×, 5×, and 10× equivalent resolution of the same region to prepare for Panoptes. (D) Panoptes architecture with optional 1 × 1 convolutional layer and clinical features branch.
Multi Resolution Cnn Architecture, supplied by Panoptes Pharma GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SoftMax Inc resnet18-softmax
Workflow and Panoptes architecture (A) A total of 456 patients in the cohorts from CPTAC and TCGA with feature annotations. (B) Overall workflow. I, H&E slide images of endometrial cancers were downloaded from databases; II, slides were separated at the per-patient level into a training, validation, and test set; III, slides were cut into 299 × 299-pixel tiles excluding background, and contaminants and qualified tiles were packaged into TFrecord files for each set; IV, training and validation sets were used to train the convolutional neural networks, and the testing set was used to evaluate trained models; V, activation maps of test set tiles were extracted and dimensionally reduced by tSNE to visualize features, while the per-tile predictions were aggregated back into intact slides; VI, an independent test set with samples from NYU hospitals was used to test the generalizability of selected best-performing models. (C) Slides were cut into paired tile sets at 2.5×, 5×, and 10× equivalent resolution of the same region to prepare for Panoptes. (D) Panoptes architecture with optional 1 × 1 convolutional layer and clinical features branch.
Resnet18 Softmax, supplied by SoftMax Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Biotechnology Information msa multiple sequence alignment bmi body mass index nb naïve bayes cnn convolutional neural network ncbi national centre
Workflow and Panoptes architecture (A) A total of 456 patients in the cohorts from CPTAC and TCGA with feature annotations. (B) Overall workflow. I, H&E slide images of endometrial cancers were downloaded from databases; II, slides were separated at the per-patient level into a training, validation, and test set; III, slides were cut into 299 × 299-pixel tiles excluding background, and contaminants and qualified tiles were packaged into TFrecord files for each set; IV, training and validation sets were used to train the convolutional neural networks, and the testing set was used to evaluate trained models; V, activation maps of test set tiles were extracted and dimensionally reduced by tSNE to visualize features, while the per-tile predictions were aggregated back into intact slides; VI, an independent test set with samples from NYU hospitals was used to test the generalizability of selected best-performing models. (C) Slides were cut into paired tile sets at 2.5×, 5×, and 10× equivalent resolution of the same region to prepare for Panoptes. (D) Panoptes architecture with optional 1 × 1 convolutional layer and clinical features branch.
Msa Multiple Sequence Alignment Bmi Body Mass Index Nb Naïve Bayes Cnn Convolutional Neural Network Ncbi National Centre, supplied by Biotechnology Information, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Panoptes Pharma GmbH panoptes-based multi-resolution cnn models
Workflow and Panoptes architecture (A) A total of 456 patients in the cohorts from CPTAC and TCGA with feature annotations. (B) Overall workflow. I, H&E slide images of endometrial cancers were downloaded from databases; II, slides were separated at the per-patient level into a training, validation, and test set; III, slides were cut into 299 × 299-pixel tiles excluding background, and contaminants and qualified tiles were packaged into TFrecord files for each set; IV, training and validation sets were used to train the convolutional neural networks, and the testing set was used to evaluate trained models; V, activation maps of test set tiles were extracted and dimensionally reduced by tSNE to visualize features, while the per-tile predictions were aggregated back into intact slides; VI, an independent test set with samples from NYU hospitals was used to test the generalizability of selected best-performing models. (C) Slides were cut into paired tile sets at 2.5×, 5×, and 10× equivalent resolution of the same region to prepare for Panoptes. (D) Panoptes architecture with optional 1 × 1 convolutional layer and clinical features branch.
Panoptes Based Multi Resolution Cnn Models, supplied by Panoptes Pharma GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Optics and Photonics paired multi-scale 3d cnn
Workflow and Panoptes architecture (A) A total of 456 patients in the cohorts from CPTAC and TCGA with feature annotations. (B) Overall workflow. I, H&E slide images of endometrial cancers were downloaded from databases; II, slides were separated at the per-patient level into a training, validation, and test set; III, slides were cut into 299 × 299-pixel tiles excluding background, and contaminants and qualified tiles were packaged into TFrecord files for each set; IV, training and validation sets were used to train the convolutional neural networks, and the testing set was used to evaluate trained models; V, activation maps of test set tiles were extracted and dimensionally reduced by tSNE to visualize features, while the per-tile predictions were aggregated back into intact slides; VI, an independent test set with samples from NYU hospitals was used to test the generalizability of selected best-performing models. (C) Slides were cut into paired tile sets at 2.5×, 5×, and 10× equivalent resolution of the same region to prepare for Panoptes. (D) Panoptes architecture with optional 1 × 1 convolutional layer and clinical features branch.
Paired Multi Scale 3d Cnn, supplied by Optics and Photonics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
IEEE Access deep multiple instance cnn
Workflow and Panoptes architecture (A) A total of 456 patients in the cohorts from CPTAC and TCGA with feature annotations. (B) Overall workflow. I, H&E slide images of endometrial cancers were downloaded from databases; II, slides were separated at the per-patient level into a training, validation, and test set; III, slides were cut into 299 × 299-pixel tiles excluding background, and contaminants and qualified tiles were packaged into TFrecord files for each set; IV, training and validation sets were used to train the convolutional neural networks, and the testing set was used to evaluate trained models; V, activation maps of test set tiles were extracted and dimensionally reduced by tSNE to visualize features, while the per-tile predictions were aggregated back into intact slides; VI, an independent test set with samples from NYU hospitals was used to test the generalizability of selected best-performing models. (C) Slides were cut into paired tile sets at 2.5×, 5×, and 10× equivalent resolution of the same region to prepare for Panoptes. (D) Panoptes architecture with optional 1 × 1 convolutional layer and clinical features branch.
Deep Multiple Instance Cnn, supplied by IEEE Access, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SoftMax Inc multi-column cnn
Workflow and Panoptes architecture (A) A total of 456 patients in the cohorts from CPTAC and TCGA with feature annotations. (B) Overall workflow. I, H&E slide images of endometrial cancers were downloaded from databases; II, slides were separated at the per-patient level into a training, validation, and test set; III, slides were cut into 299 × 299-pixel tiles excluding background, and contaminants and qualified tiles were packaged into TFrecord files for each set; IV, training and validation sets were used to train the convolutional neural networks, and the testing set was used to evaluate trained models; V, activation maps of test set tiles were extracted and dimensionally reduced by tSNE to visualize features, while the per-tile predictions were aggregated back into intact slides; VI, an independent test set with samples from NYU hospitals was used to test the generalizability of selected best-performing models. (C) Slides were cut into paired tile sets at 2.5×, 5×, and 10× equivalent resolution of the same region to prepare for Panoptes. (D) Panoptes architecture with optional 1 × 1 convolutional layer and clinical features branch.
Multi Column Cnn, supplied by SoftMax Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Kaggle Inc multi branch residual cnn
Workflow and Panoptes architecture (A) A total of 456 patients in the cohorts from CPTAC and TCGA with feature annotations. (B) Overall workflow. I, H&E slide images of endometrial cancers were downloaded from databases; II, slides were separated at the per-patient level into a training, validation, and test set; III, slides were cut into 299 × 299-pixel tiles excluding background, and contaminants and qualified tiles were packaged into TFrecord files for each set; IV, training and validation sets were used to train the convolutional neural networks, and the testing set was used to evaluate trained models; V, activation maps of test set tiles were extracted and dimensionally reduced by tSNE to visualize features, while the per-tile predictions were aggregated back into intact slides; VI, an independent test set with samples from NYU hospitals was used to test the generalizability of selected best-performing models. (C) Slides were cut into paired tile sets at 2.5×, 5×, and 10× equivalent resolution of the same region to prepare for Panoptes. (D) Panoptes architecture with optional 1 × 1 convolutional layer and clinical features branch.
Multi Branch Residual Cnn, supplied by Kaggle Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 86 stars, based on 1 article reviews
multi branch residual cnn - by Bioz Stars, 2026-06
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90
EyePACS LLC fundus imaging
Workflow and Panoptes architecture (A) A total of 456 patients in the cohorts from CPTAC and TCGA with feature annotations. (B) Overall workflow. I, H&E slide images of endometrial cancers were downloaded from databases; II, slides were separated at the per-patient level into a training, validation, and test set; III, slides were cut into 299 × 299-pixel tiles excluding background, and contaminants and qualified tiles were packaged into TFrecord files for each set; IV, training and validation sets were used to train the convolutional neural networks, and the testing set was used to evaluate trained models; V, activation maps of test set tiles were extracted and dimensionally reduced by tSNE to visualize features, while the per-tile predictions were aggregated back into intact slides; VI, an independent test set with samples from NYU hospitals was used to test the generalizability of selected best-performing models. (C) Slides were cut into paired tile sets at 2.5×, 5×, and 10× equivalent resolution of the same region to prepare for Panoptes. (D) Panoptes architecture with optional 1 × 1 convolutional layer and clinical features branch.
Fundus Imaging, supplied by EyePACS LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fundus imaging - by Bioz Stars, 2026-06
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90
Panoptes Pharma GmbH multi-resolution cnn models
Workflow and Panoptes architecture (A) A total of 456 patients in the cohorts from CPTAC and TCGA with feature annotations. (B) Overall workflow. I, H&E slide images of endometrial cancers were downloaded from databases; II, slides were separated at the per-patient level into a training, validation, and test set; III, slides were cut into 299 × 299-pixel tiles excluding background, and contaminants and qualified tiles were packaged into TFrecord files for each set; IV, training and validation sets were used to train the convolutional neural networks, and the testing set was used to evaluate trained models; V, activation maps of test set tiles were extracted and dimensionally reduced by tSNE to visualize features, while the per-tile predictions were aggregated back into intact slides; VI, an independent test set with samples from NYU hospitals was used to test the generalizability of selected best-performing models. (C) Slides were cut into paired tile sets at 2.5×, 5×, and 10× equivalent resolution of the same region to prepare for Panoptes. (D) Panoptes architecture with optional 1 × 1 convolutional layer and clinical features branch.
Multi Resolution Cnn Models, supplied by Panoptes Pharma GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/multi-resolution cnn models/product/Panoptes Pharma GmbH
Average 90 stars, based on 1 article reviews
multi-resolution cnn models - by Bioz Stars, 2026-06
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86
Kaggle Inc multiple cnn models
Workflow and Panoptes architecture (A) A total of 456 patients in the cohorts from CPTAC and TCGA with feature annotations. (B) Overall workflow. I, H&E slide images of endometrial cancers were downloaded from databases; II, slides were separated at the per-patient level into a training, validation, and test set; III, slides were cut into 299 × 299-pixel tiles excluding background, and contaminants and qualified tiles were packaged into TFrecord files for each set; IV, training and validation sets were used to train the convolutional neural networks, and the testing set was used to evaluate trained models; V, activation maps of test set tiles were extracted and dimensionally reduced by tSNE to visualize features, while the per-tile predictions were aggregated back into intact slides; VI, an independent test set with samples from NYU hospitals was used to test the generalizability of selected best-performing models. (C) Slides were cut into paired tile sets at 2.5×, 5×, and 10× equivalent resolution of the same region to prepare for Panoptes. (D) Panoptes architecture with optional 1 × 1 convolutional layer and clinical features branch.
Multiple Cnn Models, supplied by Kaggle Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 86 stars, based on 1 article reviews
multiple cnn models - by Bioz Stars, 2026-06
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90
National Institute of Standards and Technology mnist handwritten digit database
Workflow and Panoptes architecture (A) A total of 456 patients in the cohorts from CPTAC and TCGA with feature annotations. (B) Overall workflow. I, H&E slide images of endometrial cancers were downloaded from databases; II, slides were separated at the per-patient level into a training, validation, and test set; III, slides were cut into 299 × 299-pixel tiles excluding background, and contaminants and qualified tiles were packaged into TFrecord files for each set; IV, training and validation sets were used to train the convolutional neural networks, and the testing set was used to evaluate trained models; V, activation maps of test set tiles were extracted and dimensionally reduced by tSNE to visualize features, while the per-tile predictions were aggregated back into intact slides; VI, an independent test set with samples from NYU hospitals was used to test the generalizability of selected best-performing models. (C) Slides were cut into paired tile sets at 2.5×, 5×, and 10× equivalent resolution of the same region to prepare for Panoptes. (D) Panoptes architecture with optional 1 × 1 convolutional layer and clinical features branch.
Mnist Handwritten Digit Database, supplied by National Institute of Standards and Technology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Workflow and Panoptes architecture (A) A total of 456 patients in the cohorts from CPTAC and TCGA with feature annotations. (B) Overall workflow. I, H&E slide images of endometrial cancers were downloaded from databases; II, slides were separated at the per-patient level into a training, validation, and test set; III, slides were cut into 299 × 299-pixel tiles excluding background, and contaminants and qualified tiles were packaged into TFrecord files for each set; IV, training and validation sets were used to train the convolutional neural networks, and the testing set was used to evaluate trained models; V, activation maps of test set tiles were extracted and dimensionally reduced by tSNE to visualize features, while the per-tile predictions were aggregated back into intact slides; VI, an independent test set with samples from NYU hospitals was used to test the generalizability of selected best-performing models. (C) Slides were cut into paired tile sets at 2.5×, 5×, and 10× equivalent resolution of the same region to prepare for Panoptes. (D) Panoptes architecture with optional 1 × 1 convolutional layer and clinical features branch.

Journal: Cell Reports Medicine

Article Title: Predicting endometrial cancer subtypes and molecular features from histopathology images using multi-resolution deep learning models

doi: 10.1016/j.xcrm.2021.100400

Figure Lengend Snippet: Workflow and Panoptes architecture (A) A total of 456 patients in the cohorts from CPTAC and TCGA with feature annotations. (B) Overall workflow. I, H&E slide images of endometrial cancers were downloaded from databases; II, slides were separated at the per-patient level into a training, validation, and test set; III, slides were cut into 299 × 299-pixel tiles excluding background, and contaminants and qualified tiles were packaged into TFrecord files for each set; IV, training and validation sets were used to train the convolutional neural networks, and the testing set was used to evaluate trained models; V, activation maps of test set tiles were extracted and dimensionally reduced by tSNE to visualize features, while the per-tile predictions were aggregated back into intact slides; VI, an independent test set with samples from NYU hospitals was used to test the generalizability of selected best-performing models. (C) Slides were cut into paired tile sets at 2.5×, 5×, and 10× equivalent resolution of the same region to prepare for Panoptes. (D) Panoptes architecture with optional 1 × 1 convolutional layer and clinical features branch.

Article Snippet: Overall, we demonstrated that our multi-resolution CNN architecture, Panoptes, can be developed into a practical tool to assist pathologists’ classifying endometrial cancer histological subtypes and, more important, to provide additional information about patients’ molecular subtypes and mutation status in a much more rapid fashion and without the need for sequencing.

Techniques: Biomarker Discovery, Activation Assay