Evidence map›Paper›PMID 37584673›Full record

ArticleBioinformatics (Oxford, England)2023

Anomaly detection in mixed high-dimensional molecular data.

Lena Buck, Tobias Schmidt, Maren Feist, Philipp Schwarzfischer, Dieter Kube, Peter J Oefner, Helena U Zacharias, Michael Altenbuchinger, Katja Dettmer, Wolfram Gronwald and 1 more

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. 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

11 authors.

Lena BuckDepartment of Statistical Bioinformatics, University of Regensburg, 93040 Regensburg, Germany.ORCID 0000-0002-2575-6969
Tobias SchmidtDepartment of Statistical Bioinformatics, University of Regensburg, 93040 Regensburg, Germany.
Maren FeistDepartment of Hematology and Medical Oncology, University Medicine Gottingen, 37075 Gottingen, Germany.
Philipp SchwarzfischerInstitute of Functional Genomics, University of Regensburg, 93040 Regensburg, Germany.
Dieter KubeDepartment of Hematology and Medical Oncology, University Medicine Gottingen, 37075 Gottingen, Germany.
Peter J OefnerInstitute of Functional Genomics, University of Regensburg, 93040 Regensburg, Germany.
Helena U ZachariasPeter L. Reichertz Institute for Medical Informatics of TU Braunschweig and Hannover Medical School, Hannover Medical School, 30625 Hannover, Germany.
Michael AltenbuchingerDepartment of Medical Bioinformatics, University Medical Center Göttingen, 37075 Göttingen, Germany.ORCID 0000-0003-1102-6532
Katja DettmerInstitute of Functional Genomics, University of Regensburg, 93040 Regensburg, Germany.
Wolfram GronwaldInstitute of Functional Genomics, University of Regensburg, 93040 Regensburg, Germany.
Rainer SpangDepartment of Statistical Bioinformatics, University of Regensburg, 93040 Regensburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationMixed molecular data combines continuous and categorical features of the same samples, such as OMICS profiles with genotypes, diagnoses, or patient sex. Like all high-dimensional molecular data, it is prone to incorrect values that can stem from various sources for example the technical limitations of the measurement devices, errors in the sample preparation, or contamination. Most anomaly detection algorithms identify complete samples as outliers or anomalies. However, in most cases, not all measurements of those samples are erroneous but only a few one-dimensional features within the samples are incorrect. These one-dimensional data errors are continuous measurements that are either located outside or inside the normal ranges of their features but in both cases show atypical values given all other continuous and categorical features in the sample. Additionally, categorical anomalies can occur for example when the genotype or diagnosis was submitted wrongly.

resultsWe introduce ADMIRE (Anomaly Detection using MIxed gRaphical modEls), a novel approach for the detection and correction of anomalies in mixed high-dimensional data. Hereby, we focus on the detection of single (one-dimensional) data errors in the categorical and continuous features of a sample. For that the joint distribution of continuous and categorical features is learned by mixed graphical models, anomalies are detected by the difference between measured and model-based estimations and are corrected using imputation. We evaluated ADMIRE in simulation and by screening for anomalies in one of our own metabolic datasets. In simulation experiments, ADMIRE outperformed the state-of-the-art methods of Local Outlier Factor, stray, and Isolation Forest. AVAILABILITY AND IMPLEMENTATION: All data and code is available at https://github.com/spang-lab/adadmire. ADMIRE is implemented in a Python package called adadmire which can be found at https://pypi.org/project/adadmire.

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AlgorithmsSoftwareComputer SimulationGenotypeHumans

Identifiers

PMID37584673
PMCPMC10457663

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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.