Add BPNet model ENCSR108OCH (ENCSR000BQP)
Browse files- .gitattributes +5 -0
- README.md +137 -0
- config.json +45 -0
- fold_0/model.h5 +3 -0
- fold_0/saved_model/saved_model.pb +3 -0
- fold_0/saved_model/variables/variables.data-00000-of-00001 +3 -0
- fold_0/saved_model/variables/variables.index +0 -0
- fold_1/model.h5 +3 -0
- fold_1/saved_model/saved_model.pb +3 -0
- fold_1/saved_model/variables/variables.data-00000-of-00001 +3 -0
- fold_1/saved_model/variables/variables.index +0 -0
- fold_2/model.h5 +3 -0
- fold_2/saved_model/saved_model.pb +3 -0
- fold_2/saved_model/variables/variables.data-00000-of-00001 +3 -0
- fold_2/saved_model/variables/variables.index +0 -0
- fold_3/model.h5 +3 -0
- fold_3/saved_model/saved_model.pb +3 -0
- fold_3/saved_model/variables/variables.data-00000-of-00001 +3 -0
- fold_3/saved_model/variables/variables.index +0 -0
- fold_4/model.h5 +3 -0
- fold_4/saved_model/saved_model.pb +3 -0
- fold_4/saved_model/variables/variables.data-00000-of-00001 +3 -0
- fold_4/saved_model/variables/variables.index +0 -0
.gitattributes
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README.md
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| 1 |
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---
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license: cc-by-4.0
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library_name: bpnet
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tags:
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- bpnet
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- dna
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- genomics
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- transcription-factor-binding
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- chip-seq
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- encode
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- encode-bpnet-atlas
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- hg38
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- qc-passed
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- REST
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---
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# ENCODE BPNet Atlas
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As part of the ENCODE 4 Project, we trained BPNet models on 2,339 ENCODE
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transcription factor ChIP-seq experiments spanning 788 targets across
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175 biosamples. Here, we provide all models for open-source use.
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For more information about the models, see:
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- Main ENCODE 4 Paper
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- A unified lexicon of predictive DNA sequence motifs from ENCODE transcription
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factor binding and chromatin accessibility assays (Deshpande et al., Zenodo 2025)
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- Base-resolution models of transcription-factor binding reveal soft motif syntax
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(Avsec et al., Nat Genet 2021)
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## BPNet model: REST ChIP-seq in A549 (ENCSR000BQP)
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- Model: BPNet
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- Assay: TF ChIP-seq
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- Target: REST
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- Experiment: [ENCSR000BQP](https://www.encodeproject.org/experiments/ENCSR000BQP/)
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- Model annotation: [ENCSR108OCH](https://www.encodeproject.org/annotations/ENCSR108OCH/)
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- Biosample: A549 (Full name: Homo sapiens A549 treated with 0.02% ethanol for 1 hour)
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- Cell slim(s): cancer cell
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- Organ slim(s): lung
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- Developmental slim(s): endoderm
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- System slim(s): respiratory system
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- Assembly: hg38
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## QC
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- Status: passed
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- Notes: Found direct motif (counts, profile);
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## Directory structure
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5-fold cross-validation. Each `fold_*/` contains the trained BPNet model in two formats:
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- `fold_0/model.h5` — BPNet model in .h5 (Keras) format
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- `fold_0/saved_model/` — BPNet model in TensorFlow SavedModel format (a directory; load directly)
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- `config.json` — training / architecture parameters
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## Instructions
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BPNet takes a one-hot DNA sequence plus control (bias) inputs and predicts
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stranded profile logits and total logcounts. The control inputs come from the
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matched WCE/Input DNA control and **can be passed as zeros**.
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### 1. Loading the SavedModel and making predictions
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```python
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import numpy as np
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import tensorflow as tf
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from scipy.special import logsumexp
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model = tf.saved_model.load("fold_0/saved_model")
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# sequence: (N, 2114, 4) one-hot [A,C,G,T]
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# profile_bias_input: (N, 1000, 2) per-base profile bias from WCE/Input control, or zeros
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# counts_bias_input: (N, 2) log2 total counts from WCE/Input control, or zeros
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predictions = model.signatures["serving_default"](**{
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"sequence": sequence.astype("float32"),
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"profile_bias_input_0": profile_bias_input.astype("float32"),
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"counts_bias_input_0": counts_bias_input.astype("float32")})
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# predictions["profile_predictions"]: (N, 1000, 2) logits (strands NOT independent)
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# predictions["logcounts_predictions"]: (N, 1) total logcount
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output_len = 1000
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def vectorized_prediction_to_profile(predictions):
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logits_arr = predictions["profile_predictions"]
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counts_arr = predictions["logcounts_predictions"]
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pred_profile_logits = np.reshape(logits_arr, [-1, 1, output_len * 2])
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probVals_array = np.exp(pred_profile_logits - logsumexp(
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pred_profile_logits, axis=2).reshape([len(logits_arr), 1, 1]))
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profile_predictions = np.multiply(
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np.exp(counts_arr).reshape([len(counts_arr), 1, 1]), probVals_array)
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plus = np.reshape(profile_predictions, [len(counts_arr), output_len, 2])[:, :, 0]
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minus = np.reshape(profile_predictions, [len(counts_arr), output_len, 2])[:, :, 1]
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return plus, minus, counts_arr
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plus, minus, logcounts = vectorized_prediction_to_profile(predictions)
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```
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### 2. Loading the .h5 (Keras) and making predictions
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```python
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import numpy as np
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import tensorflow as tf
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import tensorflow.keras.backend as kb
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from tensorflow.keras.models import load_model
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from tensorflow.keras.utils import CustomObjectScope
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from bpnet.model.custommodel import CustomModel
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def get_model(model_path):
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with CustomObjectScope({"kb": kb, "tf": tf, "CustomModel": CustomModel}):
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return load_model(model_path)
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model = get_model("fold_0/model.h5")
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N = sequence.shape[0]
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predictions = model.predict([
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sequence, # (N, 2114, 4)
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np.zeros((N, 1000, 2)), # profile_bias_input (or real WCE/Input control values)
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np.zeros((N, 2))]) # counts_bias_input (or real control log2 counts)
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# predictions[0]: (N, 1000, 2) logits; predictions[1]: (N, 1) logcounts
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# convert with the same vectorized_prediction_to_profile() (predictions[0], predictions[1])
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```
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## Docker image to load and use the models
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`kundajelab/bpnet-atlas` (placeholder — image forthcoming).
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## Code
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- Code: https://github.com/kundajelab/bpnet/
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- Toolbox & downstream analysis: https://github.com/kundajelab/bpnet/wiki
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## License & citation
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External data users may freely download, analyze and publish results based on any
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ENCODE data without restrictions.
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Released under the ENCODE data-use policy. Please cite the ENCODE Project
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Consortium and the model software: BPNet (Avsec et al., Nat Genet 2021).
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config.json
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{
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"input_len": 2114,
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"output_profile_len": 1000,
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"motif_module_params": {
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"filters": [64],
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"kernel_sizes": [21],
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"padding": "valid"
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},
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"syntax_module_params": {
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"num_dilation_layers": 8,
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"filters": 64,
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"kernel_size": 3,
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"padding": "valid",
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"pre_activation_residual_unit": true
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},
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"profile_head_params": {
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"filters": 1,
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"kernel_size": 75,
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"padding": "valid"
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},
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"counts_head_params": {
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"filters": 1,
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"kernel_size": 75,
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"padding": "valid",
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"units": [1],
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"activations":["linear"],
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"dropouts":[0]
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},
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"profile_bias_module_params": {
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"kernel_sizes": [1]
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},
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"counts_bias_module_params": {
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},
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"use_attribution_prior": false,
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"attribution_prior_params": {
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"frequency_limit": 150,
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"limit_softness": 0.2,
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"grad_smooth_sigma": 3,
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"profile_grad_loss_weight": 200,
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"counts_grad_loss_weight": 100
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},
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"loss_weights": [1, 136.3848909575859],
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"counts_loss": "MSE"
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}
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version https://git-lfs.github.com/spec/v1
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fold_1/model.h5
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fold_1/saved_model/variables/variables.index
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|
|
|
|
|
|
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|
|
|
|
| 1 |
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version https://git-lfs.github.com/spec/v1
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|
fold_2/saved_model/variables/variables.index
ADDED
|
Binary file (5.77 kB). View file
|
|
|
fold_3/model.h5
ADDED
|
@@ -0,0 +1,3 @@
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|
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|
| 1 |
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version https://git-lfs.github.com/spec/v1
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| 3 |
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size 561784
|
fold_3/saved_model/saved_model.pb
ADDED
|
@@ -0,0 +1,3 @@
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|
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|
|
|
|
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| 1 |
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version https://git-lfs.github.com/spec/v1
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| 3 |
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size 750201
|
fold_3/saved_model/variables/variables.data-00000-of-00001
ADDED
|
@@ -0,0 +1,3 @@
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|
|
|
|
|
|
|
|
|
|
|
|
| 1 |
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version https://git-lfs.github.com/spec/v1
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| 3 |
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size 1393322
|
fold_3/saved_model/variables/variables.index
ADDED
|
Binary file (5.77 kB). View file
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|
|
fold_4/model.h5
ADDED
|
@@ -0,0 +1,3 @@
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|
|
|
|
|
|
|
|
|
|
|
|
| 1 |
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version https://git-lfs.github.com/spec/v1
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| 3 |
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size 561784
|
fold_4/saved_model/saved_model.pb
ADDED
|
@@ -0,0 +1,3 @@
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|
|
|
|
|
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|
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| 1 |
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version https://git-lfs.github.com/spec/v1
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| 3 |
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size 750201
|
fold_4/saved_model/variables/variables.data-00000-of-00001
ADDED
|
@@ -0,0 +1,3 @@
|
|
|
|
|
|
|
|
|
|
|
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|
| 1 |
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version https://git-lfs.github.com/spec/v1
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| 3 |
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size 1393322
|
fold_4/saved_model/variables/variables.index
ADDED
|
Binary file (5.77 kB). View file
|
|
|