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Add BPNet model ENCSR262LEY (ENCSR267DFA)

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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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+ 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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+ - encode
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+ - ChIP-seq
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+ - hg38
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+ - qc-passed
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+ - FOXA1
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+ ---
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+
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+ # ENCODE BPNet -- FOXA1 ChIP-seq in HepG2 (ENCSR267DFA)
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+
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+ Trained BPNet model (ChIP-seq) from the ENCODE project.
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+
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+ - Experiment: [ENCSR267DFA](https://www.encodeproject.org/experiments/ENCSR267DFA/)
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+ - Model annotation: [ENCSR262LEY](https://www.encodeproject.org/annotations/ENCSR262LEY/)
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+ - Assembly: hg38 · Target: FOXA1 · Biosample: HepG2
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+
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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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+
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+ ## Files
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+ 5-fold cross-validation. Each `fold_*/` holds the trained model in two forms:
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+ - `model.h5` — Keras weights (needs the `bpnet` custom layer to load)
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+ - `saved_model/` — TensorFlow SavedModel (portable; loads with no extra deps)
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+
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+ ## Load
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+ ```python
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+ from huggingface_hub import snapshot_download
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+ import tensorflow as tf
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+ d = snapshot_download("kundajelab/encode-bpnet-FOXA1-ChIP-seq-HepG2-ENCSR267DFA-ENCSR262LEY")
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+ model = tf.saved_model.load(f"{d}/fold_0/saved_model") # portable
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+ # Keras .h5 (needs the bpnet package):
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+ # from bpnet.model.custommodel import CustomModel
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+ # m = tf.keras.models.load_model(f"{d}/fold_0/model.h5",
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+ # custom_objects={'CustomModel': CustomModel})
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+ ```
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+
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+ ## Inference inputs
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+ The `serving_default` signature takes **three** inputs (not sequence alone):
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+ - `sequence` — one-hot DNA, shape `(N, 2114, 4)`
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+ - `profile_bias_input_0` — control (bias) profile track, shape `(N, 1000, 2)`
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+ - `counts_bias_input_0` — control log-count(s), shape `(N, 2)`
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+
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+ The bias inputs are the experiment's matched control signal (the model file's `derived_from` control bigWigs on the ENCODE portal). Outputs: `profile_predictions` `(N, 1000, 2)` and `logcounts_predictions` `(N, 1)`. Reverse-complement averaging is the production default.
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+
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+ ## License & citation
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+ Released under CC-BY-4.0, matching the [ENCODE data-use policy](https://www.encodeproject.org/about/data-use-policy/). Please cite the ENCODE Project Consortium and the model software: [BPNet](https://github.com/kundajelab/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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+ },
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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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+ },
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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, 78.55819845179451],
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+ "counts_loss": "MSE"
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+ }
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