EvoAug: improving generalization and interpretability of genomic deep neural networks with evolution-inspired data augmentations - Genome Biology

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EvoAug: improving generalization and interpretability of genomic deep neural networks with evolution-inspired data augmentations - Genome Biology
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An article published in GenomeBiology discusses EvoAug: a suite of evolution-inspired augmentations that enhance the training of genomic Deep neural networks by increasing genetic variation.

EvoAug is comprised of a set of data augmentations given by the following:

Mutation: a transformation where single nucleotide mutations are randomly applied to a given wild-type sequence. This is implemented as follows: given the hyperparameter of the fraction of nucleotides in each sequence to mutate , the number of mutations for a given sequence length is calculated; a position along the sequence is randomly sampled for each number of mutations; and the selected positions are mutagenized to a random nucleotide.

Deletion: a transformation where a random, contiguous segment of a wild-type sequence is removed, and the shortened sequence is then padded with random DNA sequence to maintain the same length as wild-type.

Inversion: a transformation where a random subsequence is replaced by its reverse-complement.

For the Basset and DeepSTARR models, each augmentation has an optimal setting that was determined from a hyperparameter search independently using the validation set . For the Basset models, the hyperparameters were set to:

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