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- README.md +120 -0
- fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.args.json +50 -0
- fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.batch_loss.tsv +0 -0
- fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.bias_formatting.stdout.txt +1 -0
- fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.chrombpnet_data_params.tsv +3 -0
- fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.chrombpnet_formatting.stdout.txt +1 -0
- fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.chrombpnet_model_params.tsv +9 -0
- fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.chrombpnet_no_bias_formatting.stdout.txt +1 -0
- fold_0/logs.models.fold_0.ENCSR749YCR/logfile.modelling.fold_0.ENCSR749YCR.epoch_loss.csv +14 -0
- fold_0/model.bias_scaled.fold_0.ENCSR749YCR.h5 +3 -0
- fold_0/model.bias_scaled.fold_0.ENCSR749YCR.tar +3 -0
- fold_0/model.chrombpnet.fold_0.ENCSR749YCR.h5 +3 -0
- fold_0/model.chrombpnet.fold_0.ENCSR749YCR.tar +3 -0
- fold_0/model.chrombpnet_nobias.fold_0.ENCSR749YCR.h5 +3 -0
- fold_0/model.chrombpnet_nobias.fold_0.ENCSR749YCR.tar +3 -0
- fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.args.json +50 -0
- fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.batch_loss.tsv +0 -0
- fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.bias_formatting.stdout.txt +1 -0
- fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.chrombpnet_data_params.tsv +3 -0
- fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.chrombpnet_formatting.stdout.txt +1 -0
- fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.chrombpnet_model_params.tsv +9 -0
- fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.chrombpnet_no_bias_formatting.stdout.txt +1 -0
- fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.epoch_loss.csv +15 -0
- fold_1/model.bias_scaled.fold_1.ENCSR749YCR.h5 +3 -0
- fold_1/model.bias_scaled.fold_1.ENCSR749YCR.tar +3 -0
- fold_1/model.chrombpnet.fold_1.ENCSR749YCR.h5 +3 -0
- fold_1/model.chrombpnet.fold_1.ENCSR749YCR.tar +3 -0
- fold_1/model.chrombpnet_nobias.fold_1.ENCSR749YCR.h5 +3 -0
- fold_1/model.chrombpnet_nobias.fold_1.ENCSR749YCR.tar +3 -0
- fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.args.json +50 -0
- fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.batch_loss.tsv +0 -0
- fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.bias_formatting.stdout.txt +1 -0
- fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.chrombpnet_data_params.tsv +3 -0
- fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.chrombpnet_formatting.stdout.txt +1 -0
- fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.chrombpnet_model_params.tsv +9 -0
- fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.chrombpnet_no_bias_formatting.stdout.txt +1 -0
- fold_2/logs.models.fold_2.ENCSR749YCR/logfile.modelling.fold_2.ENCSR749YCR.epoch_loss.csv +12 -0
- fold_2/model.bias_scaled.fold_2.ENCSR749YCR.h5 +3 -0
- fold_2/model.bias_scaled.fold_2.ENCSR749YCR.tar +3 -0
- fold_2/model.chrombpnet.fold_2.ENCSR749YCR.h5 +3 -0
- fold_2/model.chrombpnet.fold_2.ENCSR749YCR.tar +3 -0
- fold_2/model.chrombpnet_nobias.fold_2.ENCSR749YCR.h5 +3 -0
- fold_2/model.chrombpnet_nobias.fold_2.ENCSR749YCR.tar +3 -0
- fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.args.json +50 -0
- fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.batch_loss.tsv +0 -0
- fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.bias_formatting.stdout.txt +1 -0
- fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.chrombpnet_data_params.tsv +3 -0
- fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.chrombpnet_formatting.stdout.txt +1 -0
- fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.chrombpnet_model_params.tsv +9 -0
- fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.chrombpnet_no_bias_formatting.stdout.txt +1 -0
README.md
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| 1 |
+
---
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| 2 |
+
license: mit
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| 3 |
+
library_name: chrombpnet
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| 4 |
+
tags:
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| 5 |
+
- encode
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| 6 |
+
- chrombpnet
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| 7 |
+
- chromatin-accessibility
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| 8 |
+
- DNASE
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| 9 |
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- t-cell
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- hg38
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| 11 |
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---
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| 12 |
+
# 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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| 14 |
+
|
| 15 |
+
For more information about the models, see:
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| 16 |
+
- Main ENCODE 4 Paper
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| 17 |
+
- [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)
|
| 18 |
+
- [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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| 19 |
+
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| 20 |
+
## ChromBPNet model: DNASE in stimulated activated CD8-positive, alpha-beta memory T cell (ENCSR749YCR)
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| 21 |
+
- Model: ChromBPNet
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| 22 |
+
- Assay: DNASE-seq
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+
- Experiment: [ENCSR749YCR](https://www.encodeproject.org/experiments/ENCSR749YCR/)
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| 24 |
+
- Model annotation: [ENCSR712YRU](https://www.encodeproject.org/annotations/ENCSR712YRU/)
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| 25 |
+
- 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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| 26 |
+
- Cell slim(s): T-cell,CD8+-T-cell,leukocyte,hematopoietic-cell
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| 27 |
+
- Organ slim(s): bodily-fluid,blood
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| 28 |
+
- Developmental slim(s): None
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| 29 |
+
- System slim(s): immune-system
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| 30 |
+
- Assembly: hg38
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| 31 |
+
|
| 32 |
+
## Directory structure
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| 33 |
+
- `fold_0`: Model of 5-fold cross-validation: Fold 0
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| 34 |
+
- `model.chrombpnet.fold_0.encid.h5`: full chrombpnet model that combines both bias and corrected model in .h5 format
|
| 35 |
+
- `model.chrombpnet_nobias.fold_0.encid.h5`: bias-corrected accessibility model in .h5 format (Use for all biological discovery)
|
| 36 |
+
- `model.bias_scaled.fold_0.encid.h5`: bias model in .h5 format
|
| 37 |
+
- `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".
|
| 38 |
+
- `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".
|
| 39 |
+
- `model.bias_scaled.fold_0.encid.tar`: bias model in SavedModel format. After being untarred, it results in a directory named "bias_model_scaled".
|
| 40 |
+
- `logs.models.fold_0.encid`: folder containing log files for training models
|
| 41 |
+
- `fold_1`: Model of 5-fold coss-validation: Fold 1
|
| 42 |
+
- `fold_2`: Model of 5-fold cross-validation: Fold 2
|
| 43 |
+
- `fold_3`: Model of 5-fold cross-validation: Fold 3
|
| 44 |
+
- `fold_4`: Model of 5-fold cross-validation: Fold 4
|
| 45 |
+
|
| 46 |
+
# Instructions
|
| 47 |
+
## 1. Pseudocode for loading models in .h5 format
|
| 48 |
+
|
| 49 |
+
(1) Use the code in python after appropriately defining `model_in_h5_format` and `inputs`. \
|
| 50 |
+
(2) `inputs` is a one hot encoded sequence of shape (N,2114,4). Here N corresponds to the
|
| 51 |
+
number of tested sequences, 2114 is the input sequence length and 4 corresponds to [A,C,G,T].
|
| 52 |
+
|
| 53 |
+
```python
|
| 54 |
+
import tensorflow as tf
|
| 55 |
+
from tensorflow.keras.utils import get_custom_objects
|
| 56 |
+
from tensorflow.keras.models import load_model
|
| 57 |
+
|
| 58 |
+
custom_objects={"tf": tf}
|
| 59 |
+
get_custom_objects().update(custom_objects)
|
| 60 |
+
|
| 61 |
+
model=load_model(model_in_h5_format,compile=False)
|
| 62 |
+
outputs = model(inputs)
|
| 63 |
+
```
|
| 64 |
+
|
| 65 |
+
The list `outputs` consists of two elements. The first element has a shape of (N, 1000) and
|
| 66 |
+
contains logit predictions for a 1000-base-pair output. The second element, with a shape of
|
| 67 |
+
(N, 1), contains logcount predictions. To transform these predictions into per-base signals,
|
| 68 |
+
follow the provided pseudo code lines below.
|
| 69 |
+
|
| 70 |
+
```python
|
| 71 |
+
import numpy as np
|
| 72 |
+
|
| 73 |
+
def softmax(x, temp=1):
|
| 74 |
+
norm_x = x - np.mean(x,axis=1, keepdims=True)
|
| 75 |
+
return np.exp(temp*norm_x)/np.sum(np.exp(temp*norm_x), axis=1, keepdims=True)
|
| 76 |
+
|
| 77 |
+
predictions = softmax(outputs[0]) * (np.exp(outputs[1])-1)
|
| 78 |
+
```
|
| 79 |
+
|
| 80 |
+
## 2. Pseudocode for loading models in .tar format
|
| 81 |
+
|
| 82 |
+
(1) First untar the directory as follows `tar -xvf model.tar`. \
|
| 83 |
+
(2) Use the code below in python after appropriately defining `model_dir_untared` and `inputs`. \
|
| 84 |
+
(3) `inputs` is a one hot encoded sequence of shape (N,2114,4). Here N corresponds to the number
|
| 85 |
+
of tested sequences, 2114 is the input sequence length and 4 corresponds to ACGT.
|
| 86 |
+
|
| 87 |
+
Reference: https://www.tensorflow.org/api_docs/python/tf/saved_model/load
|
| 88 |
+
|
| 89 |
+
```python
|
| 90 |
+
import tensorflow as tf
|
| 91 |
+
|
| 92 |
+
model = tf.saved_model.load('model_dir_untared')
|
| 93 |
+
outputs = model.signatures['serving_default'](**{'sequence':inputs.astype('float32')})
|
| 94 |
+
```
|
| 95 |
+
|
| 96 |
+
The variable `outputs` represents a dictionary containing two key-value pairs. The first key
|
| 97 |
+
is `logits_profile_predictions`, holding a value with a shape of (N, 1000). This value corresponds
|
| 98 |
+
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)
|
| 107 |
+
|
| 108 |
+
predictions = softmax(outputs["logits_profile_predictions"]) * (np.exp(outputs["logcount_predictions"])-1)
|
| 109 |
+
```
|
| 110 |
+
|
| 111 |
+
## Docker image to load and use the models
|
| 112 |
+
- https://hub.docker.com/r/kundajelab/chrombpnet-atlas/ (tag:v1)
|
| 113 |
+
|
| 114 |
+
## Code for ChromBPNet
|
| 115 |
+
- https://github.com/kundajelab/chrombpnet/
|
| 116 |
+
|
| 117 |
+
# License & citation
|
| 118 |
+
External data users may freely download, analyze and publish results based on any ENCODE data without restrictions.
|
| 119 |
+
|
| 120 |
+
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
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| 1 |
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{
|
| 2 |
+
"cmd": "pipeline",
|
| 3 |
+
"genome": "/oak/stanford/groups/akundaje/ziwei75/atac_seq_pipeline/hg38/GRCh38_no_alt_analysis_set_GCA_000001405.15.fasta",
|
| 4 |
+
"chrom_sizes": "/oak/stanford/groups/akundaje/ziwei75/atac_seq_pipeline/hg38/GRCh38_EBV.chrom.sizes.tsv",
|
| 5 |
+
"input_bam_file": "/oak/stanford/groups/akundaje/projects/chromatin-atlas-2022/DNASE/ENCSR749YCR/preprocessing/bigWigs/ENCSR749YCR.bigWig",
|
| 6 |
+
"input_fragment_file": null,
|
| 7 |
+
"input_tagalign_file": null,
|
| 8 |
+
"output_dir": "/oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_0",
|
| 9 |
+
"data_type": "DNASE",
|
| 10 |
+
"peaks": "/oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_0/auxiliary/filtered.peaks.bed",
|
| 11 |
+
"nonpeaks": "/oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_0/auxiliary/filtered.nonpeaks.bed",
|
| 12 |
+
"chr_fold_path": "/oak/stanford/groups/akundaje/projects/chromatin-atlas-2022/splits/fold_0.json",
|
| 13 |
+
"outlier_threshold": 0.9999,
|
| 14 |
+
"ATAC_ref_path": null,
|
| 15 |
+
"DNASE_ref_path": null,
|
| 16 |
+
"num_samples": 10000,
|
| 17 |
+
"inputlen": 2114,
|
| 18 |
+
"outputlen": 1000,
|
| 19 |
+
"seed": 1234,
|
| 20 |
+
"epochs": 50,
|
| 21 |
+
"early_stop": 5,
|
| 22 |
+
"learning_rate": 0.001,
|
| 23 |
+
"trackables": [
|
| 24 |
+
"logcount_predictions_loss",
|
| 25 |
+
"loss",
|
| 26 |
+
"logits_profile_predictions_loss",
|
| 27 |
+
"val_logcount_predictions_loss",
|
| 28 |
+
"val_loss",
|
| 29 |
+
"val_logits_profile_predictions_loss"
|
| 30 |
+
],
|
| 31 |
+
"architecture_from_file": "/home/users/vhecht/chrombpnet/chrombpnet/chrombpnet/training/models/chrombpnet_with_bias_model.py",
|
| 32 |
+
"file_prefix": null,
|
| 33 |
+
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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
|
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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
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Converting /oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_0/models/chrombpnet_nobias.h5 to /oak/stanford/groups/akundaje/vhecht/chromatin-atlas-2022/DNASE/ENCSR749YCR/fold_0/new_model_format/chrombpnet_nobias.tar with get_new_tf_model_format.py
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fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.batch_loss.tsv
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fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.bias_formatting.stdout.txt
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Converting /oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_1/models/chrombpnet.h5 to /oak/stanford/groups/akundaje/vhecht/chromatin-atlas-2022/DNASE/ENCSR749YCR/fold_1/new_model_format/chrombpnet.tar with get_new_tf_model_format.py
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fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.chrombpnet_no_bias_formatting.stdout.txt
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Converting /oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_1/models/chrombpnet_nobias.h5 to /oak/stanford/groups/akundaje/vhecht/chromatin-atlas-2022/DNASE/ENCSR749YCR/fold_1/new_model_format/chrombpnet_nobias.tar with get_new_tf_model_format.py
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fold_1/logs.models.fold_1.ENCSR749YCR/logfile.modelling.fold_1.ENCSR749YCR.epoch_loss.csv
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"output_dir": "/oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_3",
|
| 9 |
+
"data_type": "DNASE",
|
| 10 |
+
"peaks": "/oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_3/auxiliary/filtered.peaks.bed",
|
| 11 |
+
"nonpeaks": "/oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_3/auxiliary/filtered.nonpeaks.bed",
|
| 12 |
+
"chr_fold_path": "/oak/stanford/groups/akundaje/projects/chromatin-atlas-2022/splits/fold_3.json",
|
| 13 |
+
"outlier_threshold": 0.9999,
|
| 14 |
+
"ATAC_ref_path": null,
|
| 15 |
+
"DNASE_ref_path": null,
|
| 16 |
+
"num_samples": 10000,
|
| 17 |
+
"inputlen": 2114,
|
| 18 |
+
"outputlen": 1000,
|
| 19 |
+
"seed": 1234,
|
| 20 |
+
"epochs": 50,
|
| 21 |
+
"early_stop": 5,
|
| 22 |
+
"learning_rate": 0.001,
|
| 23 |
+
"trackables": [
|
| 24 |
+
"logcount_predictions_loss",
|
| 25 |
+
"loss",
|
| 26 |
+
"logits_profile_predictions_loss",
|
| 27 |
+
"val_logcount_predictions_loss",
|
| 28 |
+
"val_loss",
|
| 29 |
+
"val_logits_profile_predictions_loss"
|
| 30 |
+
],
|
| 31 |
+
"architecture_from_file": "/home/users/vhecht/chrombpnet/chrombpnet/chrombpnet/training/models/chrombpnet_with_bias_model.py",
|
| 32 |
+
"file_prefix": null,
|
| 33 |
+
"html_prefix": "./",
|
| 34 |
+
"bsort": false,
|
| 35 |
+
"tmpdir": null,
|
| 36 |
+
"no_st": false,
|
| 37 |
+
"bias_model_path": "/oak/stanford/groups/akundaje/projects/chromatin-atlas-2022/reference/ENCSR283TME/fold_3/bias.h5",
|
| 38 |
+
"negative_sampling_ratio": 0.1,
|
| 39 |
+
"filters": 512,
|
| 40 |
+
"n_dilation_layers": 8,
|
| 41 |
+
"max_jitter": 500,
|
| 42 |
+
"batch_size": 64,
|
| 43 |
+
"output_prefix": "/oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_3/models/chrombpnet",
|
| 44 |
+
"bigwig": "/oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_3/auxiliary/data_unstranded.bw",
|
| 45 |
+
"plus_shift": null,
|
| 46 |
+
"minus_shift": null,
|
| 47 |
+
"chr": "chr6",
|
| 48 |
+
"pwm_width": 24,
|
| 49 |
+
"params": "/oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_3/logs/chrombpnet_model_params.tsv"
|
| 50 |
+
}
|
fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.batch_loss.tsv
ADDED
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|
|
fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.bias_formatting.stdout.txt
ADDED
|
@@ -0,0 +1 @@
|
|
|
|
|
|
|
| 1 |
+
Converting /oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_3/models/bias_model_scaled.h5 to /oak/stanford/groups/akundaje/vhecht/chromatin-atlas-2022/DNASE/ENCSR749YCR/fold_3/new_model_format/bias_model_scaled.tar with get_new_tf_model_format.py
|
fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.chrombpnet_data_params.tsv
ADDED
|
@@ -0,0 +1,3 @@
|
|
|
|
|
|
|
|
|
|
|
|
|
| 1 |
+
counts_sum_min_thresh 1.0
|
| 2 |
+
counts_sum_max_thresh 2442.21
|
| 3 |
+
trainings_pts_post_thresh 166104
|
fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.chrombpnet_formatting.stdout.txt
ADDED
|
@@ -0,0 +1 @@
|
|
|
|
|
|
|
| 1 |
+
Converting /oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_3/models/chrombpnet.h5 to /oak/stanford/groups/akundaje/vhecht/chromatin-atlas-2022/DNASE/ENCSR749YCR/fold_3/new_model_format/chrombpnet.tar with get_new_tf_model_format.py
|
fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.chrombpnet_model_params.tsv
ADDED
|
@@ -0,0 +1,9 @@
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| 1 |
+
counts_loss_weight 1.9
|
| 2 |
+
filters 512
|
| 3 |
+
n_dil_layers 8
|
| 4 |
+
bias_model_path /oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_3/models/bias_model_scaled.h5
|
| 5 |
+
inputlen 2114
|
| 6 |
+
outputlen 1000
|
| 7 |
+
max_jitter 500
|
| 8 |
+
chr_fold_path /oak/stanford/groups/akundaje/projects/chromatin-atlas-2022/splits/fold_3.json
|
| 9 |
+
negative_sampling_ratio 0.1
|
fold_3/logs.models.fold_3.ENCSR749YCR/logfile.modelling.fold_3.ENCSR749YCR.chrombpnet_no_bias_formatting.stdout.txt
ADDED
|
@@ -0,0 +1 @@
|
|
|
|
|
|
|
| 1 |
+
Converting /oak/stanford/groups/akundaje/vhecht/chromatin_atlas_bias_corrected/DNASE_model/ENCSR749YCR/fold_3/models/chrombpnet_nobias.h5 to /oak/stanford/groups/akundaje/vhecht/chromatin-atlas-2022/DNASE/ENCSR749YCR/fold_3/new_model_format/chrombpnet_nobias.tar with get_new_tf_model_format.py
|