Cited by 295Bioinformatics and Genomic NetworksCancer Genomics and DiagnosticsGene expression and cancer classification

The DOI matches its Crossref record; 88 of the 89 references it cites were found in a registry or an index, and 1 are not checked yet.

Integrative Multi-Omics Approaches in Cancer Research: From Biological Networks to Clinical Subtypes

Open access
Heo, Yong Jin, Hwa, Chanwoong, Lee, Gang-Hee, Park, Jae-Min, An, Joon-Yong·2021·Molecules and Cells

Abstract

Multi-omics approaches are novel frameworks that integrate multiple omics datasets generated from the same patients to better understand the molecular and clinical features of cancers. A wide range of emerging omics and multi-view clustering algorithms now provide unprecedented opportunities to further classify cancers into subtypes, improve the survival prediction and therapeutic outcome of these subtypes, and understand key pathophysiological processes through different molecular layers. In this review, we overview the concept and rationale of multi-omics approaches in cancer research. We also introduce recent advances in the development of multi-omics algorithms and integration methods for multiple-layered datasets from cancer patients. Finally, we summarize the latest findings from large-scale multi-omics studies of various cancers and their implications for patient subtyping and drug development.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.14348/molcells.2021.0042

Cites

88 of 89 references verified0 citation errors · 0 not checkable

Statistics

Figures

Fig. 1 Overview of multi-omics approaches in cancer research. The integration of omics datasets is a crucial step in multi-omics studies. Datasets such as somatic mutations, CNV, gene expression, methylation, and proteome datasets are merged using various computational frameworks with distinct methods. The integration enables the comparison of molecular features across multiple viewpoints and the clustering of patients with relevant clinical features. Possible outcomes include enhanced identification of clinical subtypes, understanding of cancer pathophysiology, prediction of potential drug targets, and clinical decision support.
Fig. 1 Overview of multi-omics approaches in cancer research. The integration of omics datasets is a crucial step in multi-omics studies. Datasets such as somatic mutations, CNV, gene expression, methylation, and proteome datasets are merged using various computational frameworks with distinct methods. The integration enables the comparison of molecular features across multiple viewpoints and the clustering of patients with relevant clinical features. Possible outcomes include enhanced identification of clinical subtypes, understanding of cancer pathophysiology, prediction of potential drug targets, and clinical decision support.CC BY-NC-SA · PubMed Central
Fig. 2 Latest findings in cancer multi-omics research. Multi-omics approaches integrate various high-throughput sequencing datasets across a range of molecular layers. Biological features are subject to multi-view clustering methods and account for distinct subtypes of cancer patients based on relevant clinical features.
Fig. 2 Latest findings in cancer multi-omics research. Multi-omics approaches integrate various high-throughput sequencing datasets across a range of molecular layers. Biological features are subject to multi-view clustering methods and account for distinct subtypes of cancer patients based on relevant clinical features.CC BY-NC-SA · PubMed Central

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 88 references

Cited by

Sorted by citations

See all 295

Metadata

Authors
Heo, Y. J., Hwa, C., Lee, G.-H., Park, J.-M., & An, J.-Y.
Affiliations
Korea University (KR)
Venue
Molecules and Cells
Publisher
Elsevier BV
Published
2021-07
Volume
44
Issue
7
Pages
433-443
ISSN
  • 0219-1032 (ISSN-L)
  • 1016-8478
OpenAlex
W3180571536
Cited by
294
References
88
Citations by year
2026: 66 · 2025: 81 · 2024: 75 · 2023: 56 · 2022: 15
FWCI
3.86
Type
journal article
Language
en
Open access
Locations
  • Molecules and Cells (publishedVersion, cc-by-nc-sa)
  • PubMed Central (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
Funders
National Research Foundation of Korea (2019M3E5D3073568)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer Genomics and Diagnostics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene expression and cancer classification
Keywords
multi-omics integration, cancer subtyping, multi-view clustering, biological networks, survival prediction, therapeutic outcome prediction, drug development, cancer genomics
MeSH terms
Humans, Neoplasms, Survival Analysis, Computational Biology, Biomedical Research, Metabolomics

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review