Evidence map›Paper›PMID 36005385›Full record

ArticlemSphere2022

Circular Whole-Transcriptome Amplification (cWTA) and mNGS Screening Enhanced by a Group Testing Algorithm (mEGA) Enable High-Throughput and Comprehensive Virus Identification.

Patrick Reteng, Linh Nguyen Thuy, Mizanur Rahman, Ana Maria Bispo de Filippis, Kyoko Hayashida, Tatsuki Sugi, Gabriel Gonzalez, William W Hall, Lan Anh Nguyen Thi, Junya Yamagishi

Open access · goldAbstract read
In one paragraph

Article in mSphere, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

10 authors at 4 institutions in 5 countries.

Patrick RetengDivision of Collaboration and Education, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Linh Nguyen ThuyLaboratory for Molecular Diagnostics, National Institute of Epidemiology and Health, Hanoi, Vietnam.
Mizanur RahmanEvercare Hospital Dhaka, Dhaka, Bangladesh.ORCID 0000-0002-0665-7447
Ana Maria Bispo de FilippisFlavivirus Laboratory, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro, Brazil.
Kyoko HayashidaDivision of Collaboration and Education, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Tatsuki SugiDivision of Collaboration and Education, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Gabriel GonzalezNational Virus Reference Laboratory, University College Dublin, Dublin, Ireland.
William W HallSchool of Medicine and Medical Research, University College Dublin, Dublin, Ireland.
Lan Anh Nguyen ThiLaboratory for Molecular Diagnostics, National Institute of Epidemiology and Health, Hanoi, Vietnam.
Junya YamagishiDivision of Collaboration and Education, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.ORCID 0000-0002-8385-5359
Hokkaido University · JPUniversity College Dublin · IEFundação Oswaldo Cruz · BRSquare Hospitals · BD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metagenomic next-generation sequencing (mNGS) offers a hypothesis-free approach for pathogen detection, but its applicability in clinical diagnosis, in addition to other factors, remains limited due to complicated library construction. The present study describes a PCR-free isothermal workflow for mNGS targeting RNA, based on a multiple displacement amplification, termed circular whole-transcriptome amplification (cWTA), as the template is circularized before amplification. The cWTA approach was validated with clinical samples and nanopore sequencing. Reads homologous to dengue virus 2 and chikungunya virus were detected in clinical samples from Bangladesh and Brazil, respectively. In addition, the practicality of a high-throughput detection system that combines mNGS and a group testing algorithm termed mNGS screening enhanced by a group testing algorithm (mEGA) was established. This approach enabled significant library size reduction while permitting trackability between samples and diagnostic results. Serum samples of patients with undifferentiated febrile illnesses from Vietnam (

Indexed as

Nucleic AcidsTranscriptomeAlgorithmsHigh-Throughput Nucleotide SequencingHumansRNANucleic AcidsRNAcomprehensive pathogen detectionfebrile illnessgroup testing algorithmmetagenomicmultiple displacement amplification

Identifiers

PMID36005385
PMCPMC9599668
OpenAlexW4293089114

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.