PT  - JOURNAL ARTICLE
AU  - Sayantani Basu
AU  - Roy H. Campbell
TI  - Classifying COVID-19 variants based on genetic sequences using deep learning models
AID  - 10.1101/2021.06.29.450335
DP  - 2021 Jan 01
TA  - bioRxiv
PG  - 2021.06.29.450335
4099  - http://biorxiv.org/content/early/2021/06/30/2021.06.29.450335.short
4100  - http://biorxiv.org/content/early/2021/06/30/2021.06.29.450335.full
AB  - The COrona VIrus Disease (COVID-19) pandemic led to the occurrence of several variants with time. This has led to an increased importance of understanding sequence data related to COVID-19. In this chapter, we propose an alignment-free k-mer based LSTM (Long Short-Term Memory) deep learning model that can classify 20 different variants of COVID-19. We handle the class imbalance problem by sampling a fixed number of sequences for each class label. We handle the vanishing gradient problem in LSTMs arising from long sequences by dividing the sequence into fixed lengths and obtaining results on individual runs. Our results show that one-vs-all classifiers have test accuracies as high as 92.5% with tuned hyperparameters compared to the multi-class classifier model. Our experiments show higher overall accuracies for B.1.1.214, B.1.177.21, B.1.1.7, B.1.526, and P.1 on the one-vs-all classifiers, suggesting the presence of distinct mutations in these variants. Our results show that embedding vector size and batch sizes have insignificant improvement in accuracies, but changing from 2-mers to 3-mers mostly improves accuracies. We also studied individual runs which show that most accuracies improved after the 20th run, indicating that these sequence positions may have more contributions to distinguishing among different COVID-19 variants.Competing Interest StatementThe authors have declared no competing interest.