Evidence map›Paper›PMID 29615097›Full record

ArticleBiology direct2018

Multi-omics integration for neuroblastoma clinical endpoint prediction.

Margherita Francescatto, Marco Chierici, Setareh Rezvan Dezfooli, Alessandro Zandonà, Giuseppe Jurman, Cesare Furlanello

Abstract read
In one paragraph

Article in Biology direct, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
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  3. Review
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  5. Article
  6. Advances in proteomic profiling of pediatric kidney diseases.Pediatric nephrology (Berlin, Germany) · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Liquid biopsies and cancer omics.Cell death discovery · 2020
    Review
  12. Review
  13. Review
  14. Article
  15. Article
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  17. Review
  18. Article
  19. Article
  20. The application of artificial neural networks in metabolomics: a historical perspective.Metabolomics : Official journal of the Metabolomic Society · 2019
    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

6 authors.

Margherita FrancescattoFondazione Bruno Kessler, Via Sommarive 18, Trento, 38123, Italy. francescatto@fbk.eu.
Marco ChiericiFondazione Bruno Kessler, Via Sommarive 18, Trento, 38123, Italy.
Setareh Rezvan DezfooliFondazione Bruno Kessler, Via Sommarive 18, Trento, 38123, Italy.
Alessandro ZandonàFondazione Bruno Kessler, Via Sommarive 18, Trento, 38123, Italy.
Giuseppe JurmanFondazione Bruno Kessler, Via Sommarive 18, Trento, 38123, Italy.
Cesare FurlanelloFondazione Bruno Kessler, Via Sommarive 18, Trento, 38123, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHigh-throughput methodologies such as microarrays and next-generation sequencing are routinely used in cancer research, generating complex data at different omics layers. The effective integration of omics data could provide a broader insight into the mechanisms of cancer biology, helping researchers and clinicians to develop personalized therapies.

resultsIn the context of CAMDA 2017 Neuroblastoma Data Integration challenge, we explore the use of Integrative Network Fusion (INF), a bioinformatics framework combining a similarity network fusion with machine learning for the integration of multiple omics data. We apply the INF framework for the prediction of neuroblastoma patient outcome, integrating RNA-Seq, microarray and array comparative genomic hybridization data. We additionally explore the use of autoencoders as a method to integrate microarray expression and copy number data.

conclusionsThe INF method is effective for the integration of multiple data sources providing compact feature signatures for patient classification with performances comparable to other methods. Latent space representation of the integrated data provided by the autoencoder approach gives promising results, both by improving classification on survival endpoints and by providing means to discover two groups of patients characterized by distinct overall survival (OS) curves. REVIEWERS: This article was reviewed by Djork-Arné Clevert and Tieliu Shi.

Indexed as

AnimalsComputational BiologyGene Expression ProfilingGenomicsHigh-Throughput Nucleotide SequencingHumansNeuroblastomaAutoencoderClassificationIntegrationNeuroblastomaPrediction

Identifiers

PMID29615097
PMCPMC5907722

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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.