Evidence map›Paper›PMID 35215811›Full record

ArticleViruses2022

ViralFlow: A Versatile Automated Workflow for SARS-CoV-2 Genome Assembly, Lineage Assignment, Mutations and Intrahost Variant Detection.

Filipe Zimmer Dezordi, Antonio Marinho da Silva Neto, Túlio de Lima Campos, Pedro Miguel Carneiro Jeronimo, Cleber Furtado Aksenen, Suzana Porto Almeida, Gabriel Luz Wallau, On Behalf Of The Fiocruz Covid-Genomic Surveillance Network

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
7.8field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 75 citations in OpenAlex.

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  16. Whole Genome Sequencing of DENV-2 isolated frombioRxiv : the preprint server for biology · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Filipe Zimmer DezordiDepartment of Entomology and Bioinformatics Core, Aggeu Magalhães Institute-Oswaldo Cruz Foundation (Fiocruz), Campus UFPE-Av. Prof. Moraes Rego s/n, Recife 50670-420, Brazil.
Antonio Marinho da Silva NetoBioinformatics Core, Aggeu Magalhães Institute-Oswaldo Cruz Foundation (Fiocruz), Campus UFPE-Av. Prof. Moraes Rego s/n, Recife 50670-420, Brazil.
Túlio de Lima CamposBioinformatics Core, Aggeu Magalhães Institute-Oswaldo Cruz Foundation (Fiocruz), Campus UFPE-Av. Prof. Moraes Rego s/n, Recife 50670-420, Brazil.ORCID 0000-0003-0446-848X
Pedro Miguel Carneiro JeronimoOswaldo Cruz Foundation (Fiocruz), Branch Ceará, Eusebio 61760-000, Brazil.ORCID 0000-0002-2509-5822
Cleber Furtado AksenenOswaldo Cruz Foundation (Fiocruz), Branch Ceará, Eusebio 61760-000, Brazil.
Suzana Porto AlmeidaOswaldo Cruz Foundation (Fiocruz), Branch Ceará, Eusebio 61760-000, Brazil.
Gabriel Luz WallauDepartment of Entomology and Bioinformatics Core, Aggeu Magalhães Institute-Oswaldo Cruz Foundation (Fiocruz), Campus UFPE-Av. Prof. Moraes Rego s/n, Recife 50670-420, Brazil.ORCID 0000-0002-1419-5713
On Behalf Of The Fiocruz Covid-Genomic Surveillance Network
Fundação Oswaldo Cruz · BR

Funding

Coordenação de Aperfeicoamento de Pessoal de Nível Superior Finance Code 001National Council for Scientific and Technological Development 303902/2019-1
6 · The paper itself

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.

Indexed as

Genome, ViralMutationWorkflowAutomation, LaboratoryComputational BiologyGenomicsHumansPhylogenySARS-CoV-2Spike Glycoprotein, CoronavirusVirus AssemblySpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2genomicsgenomic variantsgenotypingSARS-CoV-2softwarevirus bioinformaticsviruses

Identifiers

PMID35215811
PMCPMC8877152
OpenAlexW4206915450

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.