Evidence map›Paper›PMID 35072570›Full record

ArticleStatistical methods in medical research2022

ROSIE: RObust Sparse ensemble for outlIEr detection and gene selection in cancer omics data.

Antje Jensch, Marta B Lopes, Susana Vinga, Nicole Radde

Abstract read
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Article in Statistical methods in medical research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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. Challenges and Opportunities for Statistics in Omics Data Analysis.Advances in experimental medicine and biology · 2026
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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.

Antje JenschInstitute for Systems Theory and Automatic Control, 9149University of Stuttgart, Germany.
Marta B LopesCenter for Mathematics and Applications (CMA), NOVA School of Science and Technology, Caparica, Portugal.ORCID 0000-0002-4135-1857
Susana VingaINESC-ID, Instituto Superior Técnico, 72971Universidade de Lisboa, Portugal.ORCID 0000-0002-1954-5487
Nicole RaddeInstitute for Systems Theory and Automatic Control, 9149University of Stuttgart, Germany.ORCID 0000-0002-5145-0058

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The extraction of novel information from omics data is a challenging task, in particular, since the number of features (e.g. genes) often far exceeds the number of samples. In such a setting, conventional parameter estimation leads to ill-posed optimization problems, and regularization may be required. In addition, outliers can largely impact classification accuracy.Here we introduce ROSIE, an ensemble classification approach, which combines three sparse and robust classification methods for outlier detection and feature selection and further performs a bootstrap-based validity check. Outliers of ROSIE are determined by the rank product test using outlier rankings of all three methods, and important features are selected as features commonly selected by all methods.We apply ROSIE to RNA-Seq data from The Cancer Genome Atlas (TCGA) to classify observations into Triple-Negative Breast Cancer (TNBC) and non-TNBC tissue samples. The pre-processed dataset consists of

Indexed as

Triple Negative Breast NeoplasmsHumansbiomarkerclassificationEnsemblefeature selectionoutlierrobustsparsetriple-Negative Breast Cancer

Identifiers

PMID35072570
PMCPMC9014683

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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.