Evidence map›Paper›PMID 32005884›Full record

ArticleScientific reports2020

Performance comparison of next generation sequencing analysis pipelines for HIV-1 drug resistance testing.

Emma R Lee, Neil Parkin, Cheryl Jennings, Chanson J Brumme, Eric Enns, Maria Casadellà, Mark Howison, Mia Coetzer, Santiago Avila-Rios, Rupert Capina and 11 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
1.2field-weighted citation impact, top 12% 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

41 citing papers in PubMed, 66 citations in OpenAlex.

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  17. Full-spectrum HIV drug resistance mutation detection by high-resolution complete pol gene sequencing.Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology · 2023
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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

21 authors at 8 institutions in 4 countries.

Emma R LeeNational HIV and Retrovirology Laboratories, National Microbiology Laboratory at JC Wilt Infectious Diseases Research Centre, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
Neil ParkinData First Consulting Inc., Belmont, California, USA.
Cheryl JenningsVirology Quality Assurance Program, Rush Medical College, Chicago, USA.
Chanson J BrummeBritish Columbia Center for Excellence in HIV/AIDS, Vancouver, British Columbia, Canada.
Eric EnnsBioinformatics Core at the National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
Maria CasadellàIrsiCaixa AIDS Research Institute, Badalona, Catalonia, Spain.
Mark HowisonResearch Improving People's Lives, Providence, Rhode Island, USA.
Mia CoetzerDivision of Infectious Diseases, Brown University Alpert Medical School, Providence, Rhode Island, USA.
Santiago Avila-RiosCentre for Research in Infectious Diseases, National Institute of Respiratory Diseases, Mexico City, Mexico.
Rupert CapinaNational HIV and Retrovirology Laboratories, National Microbiology Laboratory at JC Wilt Infectious Diseases Research Centre, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
Eric MarinierBioinformatics Core at the National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
Gary Van DomselaarBioinformatics Core at the National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.ORCID http://orcid.org/0000-0003-1139-4458
Marc Noguera-JulianIrsiCaixa AIDS Research Institute, Badalona, Catalonia, Spain.ORCID http://orcid.org/0000-0002-6194-1395
Don KirkbyBritish Columbia Center for Excellence in HIV/AIDS, Vancouver, British Columbia, Canada.
Jeff KnaggsBritish Columbia Center for Excellence in HIV/AIDS, Vancouver, British Columbia, Canada.
Richard HarriganDivision of AIDS, Department of Medicine, University of British Columbia, Vancouver, Canada.
Miguel Quiñones-MateuDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Roger ParedesIrsiCaixa AIDS Research Institute, Badalona, Catalonia, Spain.ORCID http://orcid.org/0000-0002-6553-691X
Rami KantorDivision of Infectious Diseases, Brown University Alpert Medical School, Providence, Rhode Island, USA.
Paul SandstromNational HIV and Retrovirology Laboratories, National Microbiology Laboratory at JC Wilt Infectious Diseases Research Centre, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
Hezhao JiNational HIV and Retrovirology Laboratories, National Microbiology Laboratory at JC Wilt Infectious Diseases Research Centre, Public Health Agency of Canada, Winnipeg, Manitoba, Canada. hezhao.ji@canada.ca.
Public Health Agency of Canada · CAUniversity of British Columbia · CAIrsiCaixa · ESBrown University · USFirst Consulting Group (United States) · USProvidence College · USRush University Medical Center · USUniversity of Otago · NZ

Funding

Translational ScienceP30AI042853 · NIAID · MIRIAM HOSPITAL · PI CURT G BECKWITH · 1998 to 2026
$51.7M
Optimizing HIV Treatment Monitoring under Resource ConstraintsR01AI108441 · NIAID · BROWN UNIVERSITY · PI HOGAN, JOSEPH W, KANTOR, RAMI · 2015 to 2019
$3.5M
NIAID NIH HHS P30 AI042853NIAID NIH HHS R01 AI108441
6 · The paper itself

Abstract

Next generation sequencing (NGS) is a trending new standard for genotypic HIV-1 drug resistance (HIVDR) testing. Many NGS HIVDR data analysis pipelines have been independently developed, each with variable outputs and data management protocols. Standardization of such analytical methods and comparison of available pipelines are lacking, yet may impact subsequent HIVDR interpretation and other downstream applications. Here we compared the performance of five NGS HIVDR pipelines using proficiency panel samples from NIAID Virology Quality Assurance (VQA) program. Ten VQA panel specimens were genotyped by each of six international laboratories using their own in-house NGS assays. Raw NGS data were then processed using each of the five different pipelines including HyDRA, MiCall, PASeq, Hivmmer and DEEPGEN. All pipelines detected amino acid variants (AAVs) at full range of frequencies (1~100%) and demonstrated good linearity as compared to the reference frequency values. While the sensitivity in detecting low abundance AAVs, with frequencies between 1~20%, is less a concern for all pipelines, their specificity dramatically decreased at AAV frequencies <2%, suggesting that 2% threshold may be a more reliable reporting threshold for ensured specificity in AAV calling and reporting. More variations were observed among the pipelines when low abundance AAVs are concerned, likely due to differences in their NGS read quality control strategies. Findings from this study highlight the need for standardized strategies for NGS HIVDR data analysis, especially for the detection of minority HIVDR variants.

Indexed as

Amino AcidsDrug Resistance, ViralGenetic VariationGenotypeHigh-Throughput Nucleotide SequencingHIV-1HIV InfectionsHIV SeropositivityHumansSensitivity and SpecificityAmino Acids

Identifiers

PMID32005884
PMCPMC6994664
OpenAlexW3004204832

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.