A deep learning model leveraging semantic features fusion for DNase I hypersensitive sites identification in the human genome
Why this work is in the frame
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Bibliographic record
Abstract
BACKGROUND AND OBJECTIVE: DNase I hypersensitive sites (DHSs) are chromatin regions that are extremely sensitive to the DNase I enzyme, increasing their accessibility for cellular processes. DHSs are crucial for understanding transcriptional regulation mechanisms and contain genetic variations linked to various diseases such as breast cancer, coronary artery disease, Alzheimer's disease, autoimmune disorders, and neurological conditions. However, conventional DHSs identification methods are labor-intensive and resource-heavy, necessitating the need for alternative cost-effective approaches with high performance. METHODS: In this study, we propose various computational models, namely the CNN model, the CNN-GRU fusion model, the CNN-kmer fusion model, and the CNN-GRU-kmer fusion model, to overcome the challenges associated with DHSs prediction. The CNN Model is based on a simple 1-dimensional convocational neural network (CNN). The CNN-GRU fusion model is based on a simple 1-dimensional CNN and gated recurrent unit (GRU) and then fuses the feature maps of CNN and GRU. The CNN-kmer fusion model is based on a simple 1-dimensional CNN and k-mer features. First, we input the k-mer features to a dense layer; the output of the dense layer is fused with CNN features. In the CNN-GRU-kmer fusion model, based on simple 1-dimensional CNN, GRU, and k-mer features, first we input the k-mer features to a dense layer; the output of the dense layer is fused with CNN features and GRU features and fed to a dense layer with a sigmoid function for prediction. RESULTS: The proposed models were validated in the publicly available dataset, obtaining an accuracy of 0.8631, a sensitivity of 0.7209, a specificity of 0.9353, an MCC of 0.6468, an AUC ROC of 0.8528, and an AUC PR of 0.7530. These results surpass all performance evaluation metrics of state-of-the-art models. CONCLUSIONS: This study presents that the model integrates semantic vector-based feature fusion representation, which effectively captures both local and global patterns with inherited spatio-temporal dependencies within complex DHSs sequences. The model's performance was validated both with and without semantic feature fusion, followed by quantitative and statistical analyses against individual models, significantly enhancing feature representation and classification performance. Source code and datasets are available at: https://github.com/malikmtahir/DNase/tree/main.
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Full frame distilled prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.
Codex and Gemma teacher scores by category
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.002 | 0.000 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.000 |
| Bibliometrics | 0.000 | 0.000 |
| Science and technology studies | 0.000 | 0.000 |
| Scholarly communication | 0.000 | 0.000 |
| Open science | 0.000 | 0.000 |
| Research integrity | 0.000 | 0.000 |
| Insufficient payload (model declined to judge) | 0.000 | 0.000 |
Machine scores (provisional)
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it