Evidence map›Paper›PMID 34432798›Full record

ArticlePloS one2021

Oligonucleotide capture sequencing of the SARS-CoV-2 genome and subgenomic fragments from COVID-19 individuals.

Harsha Doddapaneni, Sara Javornik Cregeen, Richard Sucgang, Qingchang Meng, Xiang Qin, Vasanthi Avadhanula, Hsu Chao, Vipin Menon, Erin Nicholson, David Henke and 11 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.1field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. INTRA- AND INTER-HOST EVOLUTION OF HUMAN NOROVIRUS IN HEALTHY ADULTS.bioRxiv : the preprint server for biology · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. sgRNAs: A SARS-CoV-2 emerging issue.Aspects of molecular medicine · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Towards population-scale long-read sequencing.Nature reviews. Genetics · 2021
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 1 institution in 1 country.

Harsha DoddapaneniHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.ORCID 0000-0002-2433-633X
Sara Javornik CregeenAlkek Center for Metagenomics and Microbiome Research, Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, United States of America.
Richard SucgangAlkek Center for Metagenomics and Microbiome Research, Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, United States of America.
Qingchang MengHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
Xiang QinHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
Vasanthi AvadhanulaDepartment of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, United States of America.
Hsu ChaoHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
Vipin MenonHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
Erin NicholsonDepartment of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, United States of America.
David HenkeDepartment of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, United States of America.ORCID 0000-0003-2911-2834
Felipe-Andres PiedraDepartment of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, United States of America.
Anubama RajanDepartment of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, United States of America.ORCID 0000-0003-4773-4362
Zeineen MominHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
Kavya KottapalliHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
Kristi L HoffmanAlkek Center for Metagenomics and Microbiome Research, Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, United States of America.
Fritz J SedlazeckHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
Ginger MetcalfHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
Pedro A PiedraDepartment of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, United States of America.
Donna M MuznyHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
Joseph F PetrosinoAlkek Center for Metagenomics and Microbiome Research, Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, United States of America.
Richard A GibbsHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
Baylor College of Medicine · US

Funding

Viral Diversity and Pathogenicity in Mucosal Respiratory and Gastrointestinal DiseaseU19AI144297 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI ESTES, MARY KOLB, GIBBS, RICHARD A · 2019 to 2024
$30.1M
NIAID NIH HHS U19 AI144297NIH HHS 1U19 AI144297
6 · The paper itself

Abstract

The newly emerged and rapidly spreading SARS-CoV-2 causes coronavirus disease 2019 (COVID-19). To facilitate a deeper understanding of the viral biology we developed a capture sequencing methodology to generate SARS-CoV-2 genomic and transcriptome sequences from infected patients. We utilized an oligonucleotide probe-set representing the full-length genome to obtain both genomic and transcriptome (subgenomic open reading frames [ORFs]) sequences from 45 SARS-CoV-2 clinical samples with varying viral titers. For samples with higher viral loads (cycle threshold value under 33, based on the CDC qPCR assay) complete genomes were generated. Analysis of junction reads revealed regions of differential transcriptional activity among samples. Mixed allelic frequencies along the 20kb ORF1ab gene in one sample, suggested the presence of a defective viral RNA species subpopulation maintained in mixture with functional RNA in one sample. The associated workflow is straightforward, and hybridization-based capture offers an effective and scalable approach for sequencing SARS-CoV-2 from patient samples.

Indexed as

COVID-19DNA, ComplementaryGene FrequencyGenetic VariationGenome, ViralHumansOpen Reading FramesReal-Time Polymerase Chain ReactionRNA, ViralSARS-CoV-2Sequence Analysis, DNAViral LoadDNA, ComplementaryRNA, Viral

Identifiers

PMID34432798
PMCPMC8386831
OpenAlexW3193629630

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.