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Add BPNet model ENCSR759WXZ (ENCSR054JMQ)

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.gitattributes CHANGED
@@ -33,3 +33,8 @@ saved_model/**/* filter=lfs diff=lfs merge=lfs -text
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  *.zip filter=lfs diff=lfs merge=lfs -text
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  *.zst filter=lfs diff=lfs merge=lfs -text
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  *tfevents* filter=lfs diff=lfs merge=lfs -text
 
 
 
 
 
 
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  *.zip filter=lfs diff=lfs merge=lfs -text
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  *.zst filter=lfs diff=lfs merge=lfs -text
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  *tfevents* filter=lfs diff=lfs merge=lfs -text
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+ fold_0/saved_model/variables/variables.data-00000-of-00001 filter=lfs diff=lfs merge=lfs -text
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+ fold_1/saved_model/variables/variables.data-00000-of-00001 filter=lfs diff=lfs merge=lfs -text
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+ fold_2/saved_model/variables/variables.data-00000-of-00001 filter=lfs diff=lfs merge=lfs -text
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+ fold_3/saved_model/variables/variables.data-00000-of-00001 filter=lfs diff=lfs merge=lfs -text
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+ fold_4/saved_model/variables/variables.data-00000-of-00001 filter=lfs diff=lfs merge=lfs -text
README.md ADDED
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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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+
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+ # ENCODE BPNet Atlas
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+
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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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+
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+ For more information about the models, see:
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+
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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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+
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+ ## BPNet model: REST ChIP-seq in K562 (ENCSR054JMQ)
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+
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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: [ENCSR054JMQ](https://www.encodeproject.org/experiments/ENCSR054JMQ/)
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+ - Model annotation: [ENCSR759WXZ](https://www.encodeproject.org/annotations/ENCSR759WXZ/)
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+ - Biosample: K562 (Full name: Homo sapiens K562 genetically modified (insertion) using CRISPR targeting H. sapiens REST)
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+ - Cell slim(s): hematopoietic cell, leukocyte, cancer cell
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+ - Organ slim(s): bodily fluid, blood
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+ - Developmental slim(s): mesoderm
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+ - System slim(s): immune system
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+ - Assembly: hg38
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+
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+ ## QC
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+
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+ - Status: passed
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+ - Notes: Found direct motif (counts, profile);
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+
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+ ## Directory structure
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+
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+ 5-fold cross-validation. Each `fold_*/` contains the trained BPNet model in two formats:
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+
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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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+
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+ ## Instructions
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+
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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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+
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+ ### 1. Loading the SavedModel and making predictions
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+
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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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+
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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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+
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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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+
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+ plus, minus, logcounts = vectorized_prediction_to_profile(predictions)
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+ ```
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+
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+ ### 2. Loading the .h5 (Keras) and making predictions
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+
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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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+
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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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+
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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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+
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+ ## Docker image to load and use the models
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+
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+ `kundajelab/bpnet-atlas` (placeholder — image forthcoming).
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+
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+ ## Code
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+
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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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+
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+ ## License & citation
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+
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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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+
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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).
config.json ADDED
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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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+ "syntax_module_params": {
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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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+ "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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+ },
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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, 115.85285299806577],
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+ "counts_loss": "MSE"
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+ }
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