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  1. README.md +120 -0
  2. fold_0/logs.models.fold_0.ENCSR654UYP/logfile.modelling.fold_0.ENCSR654UYP.args.json +50 -0
  3. fold_0/logs.models.fold_0.ENCSR654UYP/logfile.modelling.fold_0.ENCSR654UYP.batch_loss.tsv +0 -0
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  12. fold_0/model.chrombpnet_nobias.fold_0.ENCSR654UYP.tar +3 -0
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  15. fold_1/logs.models.fold_1.ENCSR654UYP/logfile.modelling.fold_1.ENCSR654UYP.chrombpnet_data_params.tsv +3 -0
  16. fold_1/logs.models.fold_1.ENCSR654UYP/logfile.modelling.fold_1.ENCSR654UYP.chrombpnet_model_params.tsv +9 -0
  17. fold_1/logs.models.fold_1.ENCSR654UYP/logfile.modelling.fold_1.ENCSR654UYP.epoch_loss.csv +18 -0
  18. fold_1/model.bias_scaled.fold_1.ENCSR654UYP.h5 +3 -0
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  20. fold_1/model.chrombpnet.fold_1.ENCSR654UYP.h5 +3 -0
  21. fold_1/model.chrombpnet.fold_1.ENCSR654UYP.tar +3 -0
  22. fold_1/model.chrombpnet_nobias.fold_1.ENCSR654UYP.h5 +3 -0
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  24. fold_2/logs.models.fold_2.ENCSR654UYP/logfile.modelling.fold_2.ENCSR654UYP.args.json +23 -0
  25. fold_2/logs.models.fold_2.ENCSR654UYP/logfile.modelling.fold_2.ENCSR654UYP.batch_loss.tsv +0 -0
  26. fold_2/logs.models.fold_2.ENCSR654UYP/logfile.modelling.fold_2.ENCSR654UYP.chrombpnet_data_params.tsv +3 -0
  27. fold_2/logs.models.fold_2.ENCSR654UYP/logfile.modelling.fold_2.ENCSR654UYP.chrombpnet_model_params.tsv +9 -0
  28. fold_2/logs.models.fold_2.ENCSR654UYP/logfile.modelling.fold_2.ENCSR654UYP.epoch_loss.csv +14 -0
  29. fold_2/model.bias_scaled.fold_2.ENCSR654UYP.h5 +3 -0
  30. fold_2/model.bias_scaled.fold_2.ENCSR654UYP.tar +3 -0
  31. fold_2/model.chrombpnet.fold_2.ENCSR654UYP.h5 +3 -0
  32. fold_2/model.chrombpnet.fold_2.ENCSR654UYP.tar +3 -0
  33. fold_2/model.chrombpnet_nobias.fold_2.ENCSR654UYP.h5 +3 -0
  34. fold_2/model.chrombpnet_nobias.fold_2.ENCSR654UYP.tar +3 -0
  35. fold_3/logs.models.fold_3.ENCSR654UYP/logfile.modelling.fold_3.ENCSR654UYP.args.json +23 -0
  36. fold_3/logs.models.fold_3.ENCSR654UYP/logfile.modelling.fold_3.ENCSR654UYP.batch_loss.tsv +0 -0
  37. fold_3/logs.models.fold_3.ENCSR654UYP/logfile.modelling.fold_3.ENCSR654UYP.chrombpnet_data_params.tsv +3 -0
  38. fold_3/logs.models.fold_3.ENCSR654UYP/logfile.modelling.fold_3.ENCSR654UYP.chrombpnet_model_params.tsv +9 -0
  39. fold_3/logs.models.fold_3.ENCSR654UYP/logfile.modelling.fold_3.ENCSR654UYP.epoch_loss.csv +11 -0
  40. fold_3/model.bias_scaled.fold_3.ENCSR654UYP.h5 +3 -0
  41. fold_3/model.bias_scaled.fold_3.ENCSR654UYP.tar +3 -0
  42. fold_3/model.chrombpnet.fold_3.ENCSR654UYP.h5 +3 -0
  43. fold_3/model.chrombpnet.fold_3.ENCSR654UYP.tar +3 -0
  44. fold_3/model.chrombpnet_nobias.fold_3.ENCSR654UYP.h5 +3 -0
  45. fold_3/model.chrombpnet_nobias.fold_3.ENCSR654UYP.tar +3 -0
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  48. fold_4/logs.models.fold_4.ENCSR654UYP/logfile.modelling.fold_4.ENCSR654UYP.chrombpnet_data_params.tsv +3 -0
  49. fold_4/logs.models.fold_4.ENCSR654UYP/logfile.modelling.fold_4.ENCSR654UYP.chrombpnet_model_params.tsv +9 -0
  50. fold_4/logs.models.fold_4.ENCSR654UYP/logfile.modelling.fold_4.ENCSR654UYP.epoch_loss.csv +13 -0
README.md ADDED
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+ ---
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+ license: mit
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+ library_name: chrombpnet
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+ tags:
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+ - encode
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+ - chrombpnet
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+ - chromatin-accessibility
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+ - ATAC
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+ - breast
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+ - hg38
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+ ---
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+ # ENCODE ChromBPNet Atlas
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+ As part of the ENCODE 4 Project, we trained ChromBPNet models on 1,512 ENCODE DNAse-seq and ATAC-seq across 408 biosamples. Here, we provide all models for open-source use.
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+
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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 factor binding and chromatin accessibility assays](https://doi.org/10.5281/zenodo.17123347) (Deshpande et al., Zenodo 2025)
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+ - [ChromBPNet: bias factorized, base-resolution deep learning models of chromatin accessibility reveal cis-regulatory sequence syntax, transcription factor footprints and regulatory variants](https://doi.org/10.1101/2024.12.25.630221) (Pampari et al., bioRxiv 2024)
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+
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+ ## ChromBPNet model: ATAC in breast epithelium (ENCSR654UYP)
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+ - Model: ChromBPNet
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+ - Assay: ATAC-seq
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+ - Experiment: [ENCSR654UYP](https://www.encodeproject.org/experiments/ENCSR654UYP/)
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+ - Model annotation: [ENCSR930HKW](https://www.encodeproject.org/annotations/ENCSR930HKW/)
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+ - Biosample: breast epithelium (Full name: Homo sapiens breast epithelium tissue female adult (53 years))
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+ - Cell slim(s): None
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+ - Organ slim(s): epithelium,breast
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+ - Developmental slim(s): None
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+ - System slim(s): None
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+ - Assembly: hg38
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+
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+ ## Directory structure
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+ - `fold_0`: Model of 5-fold cross-validation: Fold 0
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+ - `model.chrombpnet.fold_0.encid.h5`: full chrombpnet model that combines both bias and corrected model in .h5 format
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+ - `model.chrombpnet_nobias.fold_0.encid.h5`: bias-corrected accessibility model in .h5 format (Use for all biological discovery)
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+ - `model.bias_scaled.fold_0.encid.h5`: bias model in .h5 format
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+ - `model.chrombpnet.fold_0.encid.tar`: full chrombpnet model that combines both bias and corrected model in SavedModel format. After being untarred, it results in a directory named "chrombpnet".
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+ - `model.chrombpnet_nobias.fold_0.encid.tar`: bias-corrected accessibility model in SavedModel format (Use for all biological discovery). After being untarred, it results in a directory named "chrombpnet_wo_bias".
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+ - `model.bias_scaled.fold_0.encid.tar`: bias model in SavedModel format. After being untarred, it results in a directory named "bias_model_scaled".
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+ - `logs.models.fold_0.encid`: folder containing log files for training models
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+ - `fold_1`: Model of 5-fold coss-validation: Fold 1
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+ - `fold_2`: Model of 5-fold cross-validation: Fold 2
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+ - `fold_3`: Model of 5-fold cross-validation: Fold 3
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+ - `fold_4`: Model of 5-fold cross-validation: Fold 4
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+
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+ # Instructions
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+ ## 1. Pseudocode for loading models in .h5 format
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+
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+ (1) Use the code in python after appropriately defining `model_in_h5_format` and `inputs`. \
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+ (2) `inputs` is a one hot encoded sequence of shape (N,2114,4). Here N corresponds to the
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+ number of tested sequences, 2114 is the input sequence length and 4 corresponds to [A,C,G,T].
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+
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+ ```python
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+ import tensorflow as tf
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+ from tensorflow.keras.utils import get_custom_objects
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+ from tensorflow.keras.models import load_model
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+
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+ custom_objects={"tf": tf}
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+ get_custom_objects().update(custom_objects)
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+
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+ model=load_model(model_in_h5_format,compile=False)
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+ outputs = model(inputs)
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+ ```
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+
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+ The list `outputs` consists of two elements. The first element has a shape of (N, 1000) and
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+ contains logit predictions for a 1000-base-pair output. The second element, with a shape of
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+ (N, 1), contains logcount predictions. To transform these predictions into per-base signals,
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+ follow the provided pseudo code lines below.
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+
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+ ```python
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+ import numpy as np
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+
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+ def softmax(x, temp=1):
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+ norm_x = x - np.mean(x,axis=1, keepdims=True)
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+ return np.exp(temp*norm_x)/np.sum(np.exp(temp*norm_x), axis=1, keepdims=True)
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+
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+ predictions = softmax(outputs[0]) * (np.exp(outputs[1])-1)
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+ ```
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+
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+ ## 2. Pseudocode for loading models in .tar format
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+
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+ (1) First untar the directory as follows `tar -xvf model.tar`. \
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+ (2) Use the code below in python after appropriately defining `model_dir_untared` and `inputs`. \
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+ (3) `inputs` is a one hot encoded sequence of shape (N,2114,4). Here N corresponds to the number
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+ of tested sequences, 2114 is the input sequence length and 4 corresponds to ACGT.
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+
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+ Reference: https://www.tensorflow.org/api_docs/python/tf/saved_model/load
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+
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+ ```python
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+ import tensorflow as tf
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+
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+ model = tf.saved_model.load('model_dir_untared')
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+ outputs = model.signatures['serving_default'](**{'sequence':inputs.astype('float32')})
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+ ```
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+
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+ The variable `outputs` represents a dictionary containing two key-value pairs. The first key
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+ is `logits_profile_predictions`, holding a value with a shape of (N, 1000). This value corresponds
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+ to logit predictions for a 1000-base-pair output. The second key, named `logcount_predictions``,
99
+ is associated with a value of shape (N, 1), representing logcount predictions. To transform these
100
+ predictions into per-base signals, utilize the provided pseudo code lines mentioned below.
101
+
102
+ ```python
103
+ import numpy as np
104
+ def softmax(x, temp=1):
105
+ norm_x = x - np.mean(x,axis=1, keepdims=True)
106
+ return np.exp(temp*norm_x)/np.sum(np.exp(temp*norm_x), axis=1, keepdims=True)
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+
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+ predictions = softmax(outputs["logits_profile_predictions"]) * (np.exp(outputs["logcount_predictions"])-1)
109
+ ```
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+
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+ ## Docker image to load and use the models
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+ - https://hub.docker.com/r/kundajelab/chrombpnet-atlas/ (tag:v1)
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+
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+ ## Code for ChromBPNet
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+ - https://github.com/kundajelab/chrombpnet/
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+
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+ # License & citation
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+ External data users may freely download, analyze and publish results based on any ENCODE data without restrictions.
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+
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+ Released under the [ENCODE data-use policy](https://www.encodeproject.org/about/data-use-policy/). Please cite the ENCODE Project Consortium and the model software: [ChromBPNet](https://github.com/kundajelab/chrombpnet) (Pampari et al., bioRxiv 2024).
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+ "cmd": "pipeline",
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+ "chr_fold_path": "/oak/stanford/groups/akundaje/cmyun/chromatlas/reference/splits/fold_0.json",
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+ "outlier_threshold": 0.9999,
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+ "ATAC_ref_path": null,
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+ "DNASE_ref_path": null,
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+ "num_samples": 10000,
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+ "inputlen": 2114,
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+ "outputlen": 1000,
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+ "seed": 1234,
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+ "epochs": 50,
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+ "early_stop": 5,
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+ "learning_rate": 0.001,
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+ "trackables": [
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+ "logcount_predictions_loss",
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+ "loss",
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+ "logits_profile_predictions_loss",
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+ "val_logcount_predictions_loss",
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+ "val_loss",
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+ "val_logits_profile_predictions_loss"
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+ "output_prefix": "/oak/stanford/groups/akundaje/cmyun/chromatlas/ATAC/ENCSR654UYP/chrombpnet_model_fold_0/models/chrombpnet",
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