Datasets:
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README.md
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## Dataset Description
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### Dataset Structure
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## Dataset Description
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To train and assess our prediction models, we assembled a comprehensive phage sequence database from diverse sources.
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As of July 9, 2023, we procured viral sequences and annotations from the RefSeq database. By isolating entries labeled 'phage', we obtained 6,075 contigs.
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Our database was further enriched with the inclusion of the TemPhD database, adding another 192,326 phage contigs extracted from 148,229 assemblies.
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To address sequence redundancy present in both the RefSeq and TemPhD databases, we applied the CD-HIT algorithm (using CD-HIT-EST with a default word size of 5).
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While several clustering thresholds (0.99, 0.95, 0.90) were experimented with and found to produce similar outcomes, we settled on a threshold of 0.99.
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This process resulted in a refined set of 40,512 distinct phage sequences, with an average length of approximately 43,356 base pairs, culminating in a total of 3.5 billion base pairs.
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Notably, these sequences target a wide spectrum of 660 bacterial genera. Subsequent to sequence curation, phage sequences were mapped to their respective bacterial hosts.
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It is a sample dataset consisting of 10,000 segments, representing random samples and segments of phage genomes.
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The full dataset is available on [Zenodo](https://zenodo.org/records/10057832).
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## Features
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- **Phage-Host Associations**: Our dataset represents bacteriophages and their bacterial hosts.
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- **Balanced Representation**: The dataset is structured to mitigate bias by evenly representing phages and their hosts across various genera, incorporating reverse-complement sequences for completeness.
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- **Dataset Composition**: The final collection includes sequences of varying lengths to accommodate different research needs, with a balanced distribution across training, validation, and testing sets.
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- **Sampling Strategy**: To ensure a comprehensive yet manageable dataset, we performed undersampling and upsampling techniques, creating a diverse array of sequence lengths and ensuring no overlap between training and testing sets at the species level.
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### Dataset Structure
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