Evidence map›Paper›PMID 36135379›Full record

ArticleMicrobiology spectrum2022

Background Filtering of Clinical Metagenomic Sequencing with a Library Concentration-Normalized Model.

Juan Du, Jingjia Zhang, Dong Zhang, Yiwen Zhou, Pengfei Wu, Wenchao Ding, Jun Wang, Chuan Ouyang, Qiwen Yang

Abstract read
In one paragraph

Article in Microbiology spectrum, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
  2. Observational
  3. Article
  4. Article
  5. Beyond the Urogenital Tract, the Role ofDiagnostics (Basel, Switzerland) · 2025
    Article
  6. Article
  7. Detection ofFrontiers in cellular and infection microbiology · 2025
    Article
  8. Article
  9. Article
  10. 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

9 authors.

Juan Du *Department of Clinical Laboratory, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospitalgrid.413106.1, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
Jingjia Zhang *Department of Clinical Laboratory, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospitalgrid.413106.1, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
Dong Zhang *Department of Clinical Laboratory, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospitalgrid.413106.1, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
Yiwen Zhou *Hangzhou Matridx Biotechnology Co., Ltd., Hangzhou, Zhejiang, China.
Pengfei WuHangzhou Matridx Biotechnology Co., Ltd., Hangzhou, Zhejiang, China.
Wenchao DingHangzhou Matridx Biotechnology Co., Ltd., Hangzhou, Zhejiang, China.
Jun WangHangzhou Matridx Biotechnology Co., Ltd., Hangzhou, Zhejiang, China.
Chuan OuyangHangzhou Matridx Biotechnology Co., Ltd., Hangzhou, Zhejiang, China.ORCID 0000-0003-1667-191X
Qiwen YangDepartment of Clinical Laboratory, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospitalgrid.413106.1, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.ORCID 0000-0001-7272-3900

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metagenomic next-generation sequencing (mNGS) can accurately detect pathogens in clinical samples. However, wet-lab contamination constrains mNGS analysis and may result in erroneous interpretation of results. Many existing methods rely on large-scale observational microbiome studies and may not be applicable to clinical mNGS tests. By generation of a pretrained profile of common laboratory contaminants, we developed an mNGS noise-filtering model based on the inverse linear relationship between microbial sequencing reads and sample library concentration, named the background elimination and correction by library concentration-normalized (BECLEAN) model. Its efficacy was evaluated with bacteria- and yeast-spiked samples and 28 cerebrospinal fluid (CSF) specimens. The diagnostic accuracy, precision, sensitivity, and specificity of BECLEAN with reference to conventional methods and diagnosis were 92.9%, 86.7%, 100%, and 86.7%, respectively. BECLEAN led to a dramatic reduction of background noise without affecting the true-positive rate and thus can provide a time-saving and convenient tool in various clinical settings.

Indexed as

MetagenomeMetagenomicsGene LibraryHigh-Throughput Nucleotide SequencingSensitivity and Specificitybackground filteringclinical settingslinear regressionmetagenomic sequencingpremodeling

Identifiers

PMID36135379
PMCPMC9603461

What OpenQuestion holds

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Registered trials

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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.