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1.
J Virol ; 98(1): e0140423, 2024 Jan 23.
Article in English | MEDLINE | ID: mdl-38088350

ABSTRACT

Coronaviruses are large RNA viruses that can infect and spread among humans and animals. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), responsible for coronavirus disease 2019, has evolved since its first detection in December 2019. Deletions are a common occurrence in SARS-CoV-2 evolution, particularly in specific genomic sites, and may be associated with the emergence of highly competent lineages. While deletions typically have a negative impact on viral fitness, some persist and become fixed in viral populations, indicating that they may confer advantageous benefits for the virus's adaptive evolution. This work presents a literature review and data analysis on structural losses in the SARS-CoV-2 genome and the potential relevance of specific signatures for enhanced viral fitness and spread.


Subject(s)
COVID-19 , SARS-CoV-2 , Animals , Humans , COVID-19/virology , Genome, Viral , SARS-CoV-2/genetics , Evolution, Molecular
2.
Viruses ; 14(2)2022 01 23.
Article in English | MEDLINE | ID: mdl-35215811

ABSTRACT

The COVID-19 pandemic is driven by Severe Acute Respiratory Syndrome coronavirus 2 (SARS-CoV-2) that emerged in 2019 and quickly spread worldwide. Genomic surveillance has become the gold standard methodology used to monitor and study this fast-spreading virus and its constantly emerging lineages. The current deluge of SARS-CoV-2 genomic data generated worldwide has put additional pressure on the urgent need for streamlined bioinformatics workflows. Here, we describe a workflow developed by our group to process and analyze large-scale SARS-CoV-2 Illumina amplicon sequencing data. This workflow automates all steps of SARS-CoV-2 reference-based genomic analysis: data processing, genome assembly, PANGO lineage assignment, mutation analysis and the screening of intrahost variants. The pipeline is capable of processing a batch of around 100 samples in less than half an hour on a personal laptop or in less than five minutes on a server with 50 threads. The workflow presented here is available through Docker or Singularity images, allowing for implementation on laptops for small-scale analyses or on high processing capacity servers or clusters. Moreover, the low requirements for memory and CPU cores and the standardized results provided by ViralFlow highlight it as a versatile tool for SARS-CoV-2 genomic analysis.


Subject(s)
Automation, Laboratory/methods , Genome, Viral , Mutation , SARS-CoV-2/classification , SARS-CoV-2/genetics , Workflow , Computational Biology/instrumentation , Computational Biology/methods , Genomics/instrumentation , Genomics/methods , Humans , Phylogeny , Spike Glycoprotein, Coronavirus/genetics , Virus Assembly/genetics
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