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type: pytorch |
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args: |
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module_file: pretrained_model_reloaded_th.py |
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module_obj: model |
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weights: |
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md5: 4878981d84499eb575abd0f3b45570d3 |
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url: https://zenodo.org/record/1466068/files/pretrained_model_reloaded_th.pth?download=1 |
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default_dataloader: |
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defined_as: kipoiseq.dataloaders.SeqIntervalDl |
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default_args: |
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alphabet_axis: 0 |
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auto_resize_len: 600 |
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dtype: np.float32 |
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dummy_axis: 2 |
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dependencies: |
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conda: |
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- python=3.6 |
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- h5py=2.10.0 |
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- _pytorch_select=0.2=gpu_0 |
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- pytorch=1.3.1=cuda100py36h53c1284_0 |
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- pip=20.3.3 |
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- pysam=0.15.3 |
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- cython=0.29.23 |
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pip: |
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- kipoiseq |
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info: |
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authors: |
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- github: davek44 |
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name: David R. Kelley |
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cite_as: https://doi.org/10.1101/gr.200535.115 |
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contributors: |
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- github: krrome |
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name: Roman Kreuzhuber |
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trained_on: "From 2,071,886 total sites, 71,886 randomly reserved for testing and 70,000 for validation, leaving 1,930,000 for training." |
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doc: "This is the Basset model published by David Kelley converted to pytorch by\ |
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\ Roman Kreuzhuber. It categorically predicts probabilities of accesible genomic\ |
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\ regions in 164 cell types (ENCODE project and Roadmap Epigenomics Consortium). Data was generated using DNAse-seq. The sequence\ |
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\ length the model uses as input is 600bp. The input of the tensor has to be (N,\ |
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\ 4, 600, 1) for N samples, 600bp window size and 4 nucleotides. Per sample, 164\ |
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\ probabilities of accessible chromatin will be predicted. \n" |
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license: MIT |
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name: Basset |
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tags: |
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- DNA accessibility |
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version: 0.1.0 |
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schema: |
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inputs: |
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associated_metadata: ranges |
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doc: DNA sequence |
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name: seq |
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shape: (4,600,1) |
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special_type: DNASeq |
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targets: |
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column_labels: |
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- target_labels.txt |
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doc: Probability of accessible chromatin in 164 cell types |
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name: DHS_probs |
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shape: (164, ) |
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test: |
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expect: |
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url: https://s3.eu-central-1.amazonaws.com/kipoi-models/predictions/14f9bf4b49e21c7b31e8f6d6b9fc69ed88e25f43/Basset/predictions.h5 |
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md5: 9df59f9899b27e65ab95426cb9557ad3 |