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  1. README.md +120 -0
  2. fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.args.json +50 -0
  3. fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.batch_loss.tsv +0 -0
  4. fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.bias_formatting.stdout.txt +1 -0
  5. fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.chrombpnet_data_params.tsv +3 -0
  6. fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.chrombpnet_formatting.stdout.txt +1 -0
  7. fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.chrombpnet_model_params.tsv +9 -0
  8. fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.chrombpnet_no_bias_formatting.stdout.txt +1 -0
  9. fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.epoch_loss.csv +14 -0
  10. fold_0/model.bias_scaled.fold_0.ENCSR749YCR.h5 +3 -0
  11. fold_0/model.bias_scaled.fold_0.ENCSR749YCR.tar +3 -0
  12. fold_0/model.chrombpnet.fold_0.ENCSR749YCR.h5 +3 -0
  13. fold_0/model.chrombpnet.fold_0.ENCSR749YCR.tar +3 -0
  14. fold_0/model.chrombpnet_nobias.fold_0.ENCSR749YCR.h5 +3 -0
  15. fold_0/model.chrombpnet_nobias.fold_0.ENCSR749YCR.tar +3 -0
  16. fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.args.json +50 -0
  17. fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.batch_loss.tsv +0 -0
  18. fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.bias_formatting.stdout.txt +1 -0
  19. fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.chrombpnet_data_params.tsv +3 -0
  20. fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.chrombpnet_formatting.stdout.txt +1 -0
  21. fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.chrombpnet_model_params.tsv +9 -0
  22. fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.chrombpnet_no_bias_formatting.stdout.txt +1 -0
  23. fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.epoch_loss.csv +15 -0
  24. fold_1/model.bias_scaled.fold_1.ENCSR749YCR.h5 +3 -0
  25. fold_1/model.bias_scaled.fold_1.ENCSR749YCR.tar +3 -0
  26. fold_1/model.chrombpnet.fold_1.ENCSR749YCR.h5 +3 -0
  27. fold_1/model.chrombpnet.fold_1.ENCSR749YCR.tar +3 -0
  28. fold_1/model.chrombpnet_nobias.fold_1.ENCSR749YCR.h5 +3 -0
  29. fold_1/model.chrombpnet_nobias.fold_1.ENCSR749YCR.tar +3 -0
  30. fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.args.json +50 -0
  31. fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.batch_loss.tsv +0 -0
  32. fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.bias_formatting.stdout.txt +1 -0
  33. fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.chrombpnet_data_params.tsv +3 -0
  34. fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.chrombpnet_formatting.stdout.txt +1 -0
  35. fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.chrombpnet_model_params.tsv +9 -0
  36. fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.chrombpnet_no_bias_formatting.stdout.txt +1 -0
  37. fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.epoch_loss.csv +12 -0
  38. fold_2/model.bias_scaled.fold_2.ENCSR749YCR.h5 +3 -0
  39. fold_2/model.bias_scaled.fold_2.ENCSR749YCR.tar +3 -0
  40. fold_2/model.chrombpnet.fold_2.ENCSR749YCR.h5 +3 -0
  41. fold_2/model.chrombpnet.fold_2.ENCSR749YCR.tar +3 -0
  42. fold_2/model.chrombpnet_nobias.fold_2.ENCSR749YCR.h5 +3 -0
  43. fold_2/model.chrombpnet_nobias.fold_2.ENCSR749YCR.tar +3 -0
  44. fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.args.json +50 -0
  45. fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.batch_loss.tsv +0 -0
  46. fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.bias_formatting.stdout.txt +1 -0
  47. fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.chrombpnet_data_params.tsv +3 -0
  48. fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.chrombpnet_formatting.stdout.txt +1 -0
  49. fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.chrombpnet_model_params.tsv +9 -0
  50. fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.chrombpnet_no_bias_formatting.stdout.txt +1 -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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+ - DNASE
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+ - t-cell
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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: DNASE in stimulated activated CD8-positive, alpha-beta memory T cell (ENCSR749YCR)
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+ - Model: ChromBPNet
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+ - Assay: DNASE-seq
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+ - Experiment: [ENCSR749YCR](https://www.encodeproject.org/experiments/ENCSR749YCR/)
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+ - Model annotation: [ENCSR712YRU](https://www.encodeproject.org/annotations/ENCSR712YRU/)
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+ - Biosample: stimulated activated CD8-positive, alpha-beta memory T cell (Full name: Homo sapiens stimulated activated CD8-positive, alpha-beta memory T cell male adult (38 years) treated with anti-CD3 and anti-CD28 coated beads for 1 hour, 100 ng/mL Interleukin-7 for 1 hour)
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+ - Cell slim(s): T-cell,CD8+-T-cell,leukocyte,hematopoietic-cell
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+ - Organ slim(s): bodily-fluid,blood
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+ - Developmental slim(s): None
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+ - System slim(s): immune-system
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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``,
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+ 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.
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+
102
+ ```python
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+ import numpy as np
104
+ 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["logits_profile_predictions"]) * (np.exp(outputs["logcount_predictions"])-1)
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+ ```
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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).
fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.args.json ADDED
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+ {
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+ "cmd": "pipeline",
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+ "genome": "/oak/stanford/groups/akundaje/ziwei75/atac_seq_pipeline/hg38/GRCh38_no_alt_analysis_set_GCA_000001405.15.fasta",
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+ "output_dir": "/oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_0",
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+ "data_type": "DNASE",
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+ "chr_fold_path": "/oak/stanford/groups/akundaje/projects/chromatin-atlas-2022/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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+ ],
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+ "architecture_from_file": "/home/users/vhecht/chrombpnet/chrombpnet/chrombpnet/training/models/chrombpnet_with_bias_model.py",
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+ "file_prefix": null,
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+ "html_prefix": "./",
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+ "negative_sampling_ratio": 0.1,
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+ "filters": 512,
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+ "n_dilation_layers": 8,
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+ "max_jitter": 500,
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+ "batch_size": 64,
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+ "output_prefix": "/oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_0/models/chrombpnet",
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+ "bigwig": "/oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_0/auxiliary/data_unstranded.bw",
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+ "plus_shift": null,
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+ "minus_shift": null,
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+ "chr": "chr8",
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+ "pwm_width": 24,
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+ "params": "/oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_0/logs/chrombpnet_model_params.tsv"
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+ }
fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.batch_loss.tsv ADDED
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+ Converting /oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_0/models/bias_model_scaled.h5 to /oak/stanford/groups/akundaje/vhecht/chromatin-atlas-2022/DNASE/ENCSR749YCR/fold_0/new_model_format/bias_model_scaled.tar with get_new_tf_model_format.py
fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.chrombpnet_data_params.tsv ADDED
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+ counts_sum_min_thresh 1.0
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+ counts_sum_max_thresh 2413.66
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+ trainings_pts_post_thresh 165851
fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.chrombpnet_formatting.stdout.txt ADDED
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+ Converting /oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_0/models/chrombpnet.h5 to /oak/stanford/groups/akundaje/vhecht/chromatin-atlas-2022/DNASE/ENCSR749YCR/fold_0/new_model_format/chrombpnet.tar with get_new_tf_model_format.py
fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.chrombpnet_model_params.tsv ADDED
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+ counts_loss_weight 1.9
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+ filters 512
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+ n_dil_layers 8
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+ bias_model_path /oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_0/models/bias_model_scaled.h5
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+ inputlen 2114
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+ outputlen 1000
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+ max_jitter 500
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+ chr_fold_path /oak/stanford/groups/akundaje/projects/chromatin-atlas-2022/splits/fold_0.json
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+ negative_sampling_ratio 0.1
fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.chrombpnet_no_bias_formatting.stdout.txt ADDED
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