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README.md ADDED
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+ ---
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+ # For reference on model card metadata, see the spec: https://github.com/huggingface/hub-docs/blob/main/datasetcard.md?plain=1
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+ # Doc / guide: https://huggingface.co/docs/hub/datasets-cards
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+ {}
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+ ---
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+
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+ # Dataset Card for Dataset Name
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+ The `nucleotide_transformer_downstream_tasks` dataset features the 18 downstream tasks presented in the Nucleotide Transformer paper. They consist of both binary and multi-class classification tasks that aim at providing a consistent genomics benchmark.
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+
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+
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+ ## Dataset Description
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+
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+ - **Repository:** [Nucleotide Transformer](https://github.com/instadeepai/nucleotide-transformer)
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+ - **Paper:** [The Nucleotide Transformer: Building and Evaluating Robust Foundation Models for Human Genomics](https://www.biorxiv.org/content/10.1101/2023.01.11.523679v1)
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+
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+ ### Dataset Summary
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+
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+ The different datasets are collected from 4 different genomics papers:
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+ - [DeePromoter: Robust Promoter Predictor Using Deep Learning](https://www.frontiersin.org/articles/10.3389/fgene.2019.00286/full): The datasets features 3,065 TATA promoters and 26,532 non-TATA promoters, with each promoter yielding a negative sequence by randomly sampling parts of the sequence. The `promoter_all` dataset will feature all the promoters and their negative counterparts, while the `promoter_tata` and `promoter_no_tata` respectively provide the TATA and non-TATA parts of the dataset.
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+ - [A deep learning framework for enhancer prediction using word embedding and sequence generation](https://www.sciencedirect.com/science/article/abs/pii/S0301462222000643): To build the training dataset, the authors collect 742 strong
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+ enhancers, 742 weak enhancers and 1484 non-enhancers, and augment the dataset with 6000 synthetic enhancers and 6000 synthetic non-enhancers produced with a generative model. The test dataset is comprised of 100 strong enhancers, 100 weak enhancers and 200 non enhancers. The original paper uses this dataset to do both binary classification (i.e a sample gets classified as non-enhancer or enhancer) and 3-class classification (i.e a sample gets classified as non-enhancer, weak enhancer or strong enhancer). Both tasks are respectively tackled in the `enhancers` and `enhancers_types` datasets.
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+ - [SpliceFinder: ab initio prediction of splice sites using convolutional neural network](https://pubmed.ncbi.nlm.nih.gov/31881982): The authors introduce a dataset containing 10,000 samples of donor site, acceptor site, and non-splice-site, resulting in 30,000 total samples that are featured in the `splice_sites_all` dataset.
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+ - [Spliceator: multi-species splice site prediction using convolutional neural networks](https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-021-04471-3): Two datasets are introduced by this paper, each of them contain splice sites and their corresponding negative datasets. The dataset `splice_sites_acceptor` features acceptor splice sites and the other, `splice_sites_donor`, donor splice sites.
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+ - [Qualitatively predicting acetylation and methylation areas in DNA sequences](https://pubmed.ncbi.nlm.nih.gov/16901084/): The paper introduces a set of datasets featuring epigenetic marks identified in the yeast genome, namely acetylation and metylation nucleosome occupancies. Nucleosome occupancy values in these ten datasets were obtained with Chip-Chip experiments and further processed into positive and negative observations to provide the datasets corresponding to the following histone marks: `H3`, `H4`, `H3K9ac`, `H3K14ac`, `H4ac`, `H3K4me1`, `H3K4me2`, `H3K4me3`, `H3K36me3` and `H3K79me3`
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+
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+ ## Dataset Structure
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+ ```
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+ | Task | Number of train sequences | Number of test sequences | Number of labels | Sequence length |
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+ | --------------------- | ------------------------- | ------------------------ | ---------------- | --------------- |
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+ | promoter_all | 30,000 | 1,584 | 2 | 300 |
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+ | promoter_tata | 5,062 | 212 | 2 | 300 |
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+ | promoter_no_tata | 30,000 | 1,372 | 2 | 300 |
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+ | enhancers | 30,000 | 3,000 | 2 | 400 |
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+ | enhancers_types | 30,000 | 3,000 | 3 | 400 |
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+ | splice_sites_all | 30,000 | 3,000 | 3 | 600 |
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+ | splice_sites_acceptor | 30,000 | 3,000 | 2 | 600 |
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+ | splice_sites_donor | 30,000 | 3,000 | 2 | 600 |
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+ | H2AFZ | 30,000 | 3,000 | 2 | 1,000 |
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+ | H3K27ac | 30,000 | 1,616 | 2 | 1,000 |
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+ | H3K27me3 | 30,000 | 3,000 | 2 | 1,000 |
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+ | H3K36me3 | 30,000 | 3,000 | 2 | 1,000 |
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+ | H3K4me1 | 30,000 | 3,000 | 2 | 1,000 |
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+ | H3K4me2 | 30,000 | 2,138 | 2 | 1,000 |
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+ | H3K4me3 | 30,000 | 776 | 2 | 1,000 |
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+ | H3K9ac | 23,274 | 1,004 | 2 | 1,000 |
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+ | H3K9me3 | 27,438 | 850 | 2 | 1,000 |
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+ | H4K20me1 | 30,000 | 2,270 | 2 | 1,000 |
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+ ```
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+
nucleotide_transformer_downstream_tasks_v2.py → nucleotide_transformer_downstream_tasks_revised.py RENAMED
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