Evidence map›Paper›PMID 40794770›Full record

ReviewCancer research2025

Challenges and Opportunities in Analyzing Cancer-Associated Microbiomes.

Minghao Chia, Mihai Pop, Steven L Salzberg, Niranjan Nagarajan

Abstract readReview
In one paragraph

Review in Cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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

4 authors.

Minghao ChiaGenome Institute of Singapore (GIS), Agency for Science, Technology and Research (A*STAR), Genome, Singapore, Republic of Singapore.ORCID 0000-0001-6473-9881
Mihai PopDepartment of Computer Science, University of Maryland Institute for Advanced Computer Studies (UMIACS), University of Maryland, College Park, Maryland.ORCID 0000-0001-9617-5304
Steven L SalzbergCenter for Computational Biology, Johns Hopkins University, Baltimore, Maryland.ORCID 0000-0002-8859-7432
Niranjan NagarajanGenome Institute of Singapore (GIS), Agency for Science, Technology and Research (A*STAR), Genome, Singapore, Republic of Singapore.ORCID 0000-0003-0850-5604

Funding

Computational Methods for Genome Assembly, Transcript Assembly, and Variant DiscoveryR01HG006677 · NHGRI · JOHNS HOPKINS UNIVERSITY · PI SALZBERG, STEVEN L. · 2011 to 2025
$10.7M
Computational Methods for Microbial and Microbiome Sequence AnalysisR35GM130151 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Steven L. Salzberg · 2019 to 2026
$2.9M
National Human Genome Research Institute (NHGRI) R01-HG006677National Institute of General Medical Sciences (NIGMS) R35-GM130151National Medical Research Council (NMRC) OFYIRG21nov-0024National Research Foundation Singapore (NRF) NRFI09-0015NHGRI NIH HHS R01 HG006677NIGMS NIH HHS R35 GM130151
6 · The paper itself

Abstract

The study of cancer-associated microbiomes has gained significant attention in recent years, spurred by advances in high-throughput sequencing and metagenomic analysis. Microbiome research holds promise for identifying noninvasive biomarkers and possibly new paradigms for cancer treatment. In this review, we explore the key computational challenges and opportunities in analyzing cancer-associated microbiomes (in tumor/normal tissues and other body sites, e.g., gut, oral, and skin), focusing on sequencing-driven strategies and associated considerations for taxonomic and functional characterization. The discussion covers the strengths and limitations of current analysis tools for identifying contamination, determining compositional bias, and resolving species and strains, as well as the statistical, metabolic, and network inferences that are essential to uncover host-microbiome interactions. Several key considerations are required to guide the choice of databases used for metagenomic analysis in such studies. Recent advances in spatial and single-cell technologies have provided insights into cancer-associated microbiomes, and Artificial Intelligence-driven protein function prediction might enable rapid advances in this field. Finally, we provide a perspective on how the field can evolve to manage the ever-growing size of datasets and generate robust and testable hypotheses. This article is part of a special series: Driving Cancer Discoveries with Computational Research, Data Science, and Machine Learning/AI .

Indexed as

MetagenomicsMicrobiotaNeoplasmsComputational BiologyHigh-Throughput Nucleotide SequencingHumans

Identifiers

PMID40794770
PMCPMC12419811

What OpenQuestion holds

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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.