Evidence map›Paper›PMID 40258039›Full record

ArticlePLOS global public health2025

Diagnostic yield of nine user-friendly bioinformatics tools for predicting Mycobacterium tuberculosis drug resistance: A systematic review and network meta-analysis.

Ya-Li Chen, Yu He, Victor Naestholt Dahl, Kan Yu, Yan-An Zhang, Cui-Ping Guan, Mao-Shui Wang

Abstract read
In one paragraph

Article in PLOS global public health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Open-access genomic drug resistance prediction tools forJournal of clinical microbiology · 2026
    Pooled it
  2. Review
  3. Article
  4. Review
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

7 authors.

Ya-Li ChenDepartment of Lab Medicine, Shandong Public Health Clinical Center, Shandong University, Jinan, China.ORCID https://orcid.org/0009-0007-7829-8002
Yu HeDepartment of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Victor Naestholt DahlDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.ORCID https://orcid.org/0000-0003-2965-6348
Kan YuThe Marshall Centre for Infectious Diseases, Research and Training, The University of Western Australia, Perth, Western Australia, Australia.
Yan-An ZhangShandong Key Laboratory of Infectious Respiratory Disease, Shandong Provincial Health Commission, Jinan, China.
Cui-Ping GuanDepartment of Lab Medicine, Shandong Public Health Clinical Center, Shandong University, Jinan, China.
Mao-Shui WangDepartment of Lab Medicine, Shandong Public Health Clinical Center, Shandong University, Jinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To compare the diagnostic yield of various bioinformatics tools for predicting Mycobacterium tuberculosis drug resistance. A systematic review of PubMed, Embase, Scopus, Web of Science, CINAHL and the Cochrane Library was performed to identify studies reporting the effectiveness of bioinformatic tools for predicting resistance to anti-tuberculosis (TB) drugs. Data were collected and pooled using random-effects meta-analysis and Bayesian network meta-analysis (NMA). Summary receiver operating characteristic curves (SROCs) analysis were performed, and superiority index (SI) and area under the curve (AUC) were calculated. Thirty-three studies evaluated 9 different bioinformatics tools for predicting resistance to 14 anti-TB drugs. NMA and SROCs demonstrated that TBProfiler, TGS-TB, Mykrobe, PhyResSE, and SAM-TB all exhibited satisfactory performance. Remarkably, TBProfiler stood out with its exceptional ability to predict resistance to the majority of anti-TB drugs, including isoniazid (SI: 3.39 [95% confidence interval (CI): 0.20, 11.00]; AUC: 0.97 [0.95, 0.98]), rifampicin (SI: 6.38 [0.60, 15.00]; AUC: 0.99 [0.98, 1.00]), ethambutol (SI: 5.15 [0.60, 13.00]; AUC: 0.96 [0.94, 0.97]), streptomycin (SI: 3.67 [0.60, 11.00]; AUC: 0.97 [0.95, 0.98], amikacin (SI: 2.49 [0.14, 11.00]; AUC: 0.97 [0.96, 0.99]), kanamycin (SI: 2.26 [0.14, 9.00]; AUC: 0.98 [0.97, 0.99]), levofloxacin (SI: 1.87 [0.11, 9.00]; AUC: 0.95 [0.93, 0.97]), and prothionamide (SI: 2.73 [0.20, 7.00]; AUC: 0.87 [0.84, 0.90]). Meanwhile, Mykrobe demonstrated superior accuracy specifically for moxifloxacin (SI: 3.96 [0.11, 13.00]; AUC: 0.97 [0.95, 0.98]). Lastly, TGS-TB had the best efficacy in predicting resistance to pyrazinamide (SI: 12.53 [1.67, 17.00]; AUC: 0.97 [0.95, 0.98]), capreomycin (SI: 4.22 [0.08, 15.00]; AUC: 1.00 [0.98, 1.00]), and ethionamide (SI: 2.15 [0.33, 7.00]; AUC: 0.96 [0.94, 0.98]). TBProfiler, TGS-TB, Mykrobe, PhyResSE and SAM-TB have all demonstrated outstanding accuracy in predicting resistance to anti-TB drugs. In particular, TBProfiler stood out for its exceptional performance in predicting resistance to most anti-TB drugs, while TGS-TB excelled in predicting resistance to pyrazinamide and certain second-line drugs. The efficacy of SAM-TB requires further investigation to fully establish its reliability and effectiveness. To ensure the accuracy and reliability of genotypic drug susceptibility testing, bioinformatics tools should be refined and adapted continuously to accommodate novel and current resistance-associated mutations.

Identifiers

PMID40258039
PMCPMC12011222

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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.