Evidence map›Paper›PMID 31861998›Full record

ArticleBMC bioinformatics2019

Challenges in proteogenomics: a comparison of analysis methods with the case study of the DREAM proteogenomics sub-challenge.

Tara Eicher, Andrew Patt, Esko Kautto, Raghu Machiraju, Ewy Mathé, Yan Zhang

Abstract readComparative Study
In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Synthetic data generation with probabilistic Bayesian Networks.Mathematical biosciences and engineering : MBE · 2021
    Article
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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

6 authors.

Tara EicherDepartment of Computer Science and Engineering, The Ohio State University, Columbus, OH, 43210, USA.
Andrew PattDepartment of Biomedical Informatics, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Esko KauttoDepartment of Biomedical Informatics, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Raghu MachirajuDepartment of Computer Science and Engineering, The Ohio State University, Columbus, OH, 43210, USA. machiraju.1@osu.edu.
Ewy MathéDepartment of Biomedical Informatics, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA. ewy.mathe@osumc.edu.
Yan ZhangDepartment of Biomedical Informatics, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA. yan.zhang@osumc.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProteomic measurements, which closely reflect phenotypes, provide insights into gene expression regulations and mechanisms underlying altered phenotypes. Further, integration of data on proteome and transcriptome levels can validate gene signatures associated with a phenotype. However, proteomic data is not as abundant as genomic data, and it is thus beneficial to use genomic features to predict protein abundances when matching proteomic samples or measurements within samples are lacking.

resultsWe evaluate and compare four data-driven models for prediction of proteomic data from mRNA measured in breast and ovarian cancers using the 2017 DREAM Proteogenomics Challenge data. Our results show that Bayesian network, random forests, LASSO, and fuzzy logic approaches can predict protein abundance levels with median ground truth-predicted correlation values between 0.2 and 0.5. However, the most accurately predicted proteins differ considerably between approaches.

conclusionsIn addition to benchmarking aforementioned machine learning approaches for predicting protein levels from transcript levels, we discuss challenges and potential solutions in state-of-the-art proteogenomic analyses.

Indexed as

ProteogenomicsBayes TheoremGene Expression RegulationHumansProteomeRNA, MessengerTranscriptomeProteomeRNA, MessengerBayesian networksFuzzy logicmRNAProteogenomicsRandom forests

Identifiers

PMID31861998
PMCPMC6923881

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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.