Evidence map›Paper›PMID 38570615›Full record

ArticleCommunications biology2024

Multi-Attribute Subset Selection enables prediction of representative phenotypes across microbial populations.

Konrad Herbst, Taiyao Wang, Elena J Forchielli, Meghan Thommes, Ioannis Ch Paschalidis, Daniel Segrè

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Explainable rule-based prediction of cultivation media for microbes.Computational and structural biotechnology journal · 2025
    Article
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.

Konrad Herbst *Bioinformatics Program, Boston University, Boston, MA, USA.ORCID 0000-0003-1296-1522
Taiyao Wang *Division of Systems Engineering, Boston University, Boston, MA, USA.ORCID 0000-0002-0331-3892
Elena J Forchielli *Biological Design Center, Boston University, Boston, MA, USA.
Meghan Thommes *Biological Design Center, Boston University, Boston, MA, USA.
Ioannis Ch PaschalidisDivision of Systems Engineering, Boston University, Boston, MA, USA. yannisp@bu.edu.ORCID 0000-0002-3343-2913
Daniel SegrèBioinformatics Program, Boston University, Boston, MA, USA. dsegre@bu.edu.ORCID 0000-0003-4859-1914

Funding

Identifying protective omics profiles in centenarians and translating these into preventive and therapeutic strategiesUH2AG064704 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI PERLS, THOMAS T, SEBASTIANI, PAOLA · 2019 to 2021
$9.4M
NIA NIH HHS UH2 AG064704
6 · The paper itself

Abstract

The interpretation of complex biological datasets requires the identification of representative variables that describe the data without critical information loss. This is particularly important in the analysis of large phenotypic datasets (phenomics). Here we introduce Multi-Attribute Subset Selection (MASS), an algorithm which separates a matrix of phenotypes (e.g., yield across microbial species and environmental conditions) into predictor and response sets of conditions. Using mixed integer linear programming, MASS expresses the response conditions as a linear combination of the predictor conditions, while simultaneously searching for the optimally descriptive set of predictors. We apply the algorithm to three microbial datasets and identify environmental conditions that predict phenotypes under other conditions, providing biologically interpretable axes for strain discrimination. MASS could be used to reduce the number of experiments needed to identify species or to map their metabolic capabilities. The generality of the algorithm allows addressing subset selection problems in areas beyond biology.

Indexed as

AlgorithmsPhenotype

Identifiers

PMID38570615
PMCPMC10991586

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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.