Deep learning forward and reverse primer design to detect SARS-CoV-2 emerging variants. (arXiv:2209.13591v1 [q-bio.GN])

Surges that have been observed at different periods in the number of COVID-19
cases are associated with the emergence of multiple SARS-CoV-2 (Severe Acute
Respiratory Virus) variants. The design of methods to support laboratory
detection are crucial in the monitoring of these variants. Hence, in this
paper, we develop a semi-automated method to design both forward and reverse
primer sets to detect SARS-CoV-2 variants. To proceed, we train deep
Convolution Neural Networks (CNNs) to classify labelled SARS-CoV-2 variants and
identify partial genomic features needed for the forward and reverse Polymerase
Chain Reaction (PCR) primer design. Our proposed approach supplements existing
ones while promoting the emerging concept of neural network assisted primer
design for PCR. Our CNN model was trained using a database of SARS-CoV-2
full-length genomes from GISAID and tested on a separate dataset from NCBI,
with 98% accuracy for the classification of variants. This result is based on
the development of three different methods of feature extraction, and the
selected primer sequences for each SARS-CoV-2 variant detection (except
Omicron) were present in more than 95 % of sequences in an independent set of
5000 same variant sequences, and below 5 % in other independent datasets with
5000 sequences of each variant. In total, we obtain 22 forward and reverse
primer pairs with flexible length sizes (18-25 base pairs) with an expected
amplicon length ranging between 42 and 3322 nucleotides. Besides the feature
appearance, in-silico primer checks confirmed that the identified primer pairs
are suitable for accurate SARS-CoV-2 variant detection by means of PCR tests.

Source: https://arxiv.org/abs/2209.13591

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