Evidence map›Paper›PMID 38940181›Full record

ArticleBioinformatics (Oxford, England)2024

Adaptive digital tissue deconvolution.

Franziska Görtler, Malte Mensching-Buhr, Ørjan Skaar, Stefan Schrod, Thomas Sterr, Andreas Schäfer, Tim Beißbarth, Anagha Joshi, Helena U Zacharias, Sushma Nagaraja Grellscheid and 1 more

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. 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

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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. HIDE: hierarchical cell-type deconvolution.Bioinformatics (Oxford, England) · 2025
    Article
  4. Virtual tissue expression analysis.Bioinformatics (Oxford, England) · 2024
    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

11 authors.

Franziska GörtlerComputational Biology Unit, Department of Biological Sciences, University of Bergen, N-5008 Bergen, Norway.ORCID 0000-0003-2015-5766
Malte Mensching-BuhrDepartment of Medical Bioinformatics, University Medical Center Göttingen, 37075 Göttingen, Germany.
Ørjan SkaarDepartment of Informatics, Computational Biology Unit, University of Bergen, N-5008 Bergen, Norway.
Stefan SchrodDepartment of Medical Bioinformatics, University Medical Center Göttingen, 37075 Göttingen, Germany.ORCID 0000-0001-9936-3984
Thomas SterrInstitute of Theoretical Physics, University of Regensburg, 93053 Regensburg, Germany.
Andreas SchäferInstitute of Theoretical Physics, University of Regensburg, 93053 Regensburg, Germany.
Tim BeißbarthDepartment of Medical Bioinformatics, University Medical Center Göttingen, 37075 Göttingen, Germany.ORCID 0000-0001-6509-2143
Anagha JoshiDepartment of Clinical Science, Computational Biology Unit, University of Bergen, N-5008 Bergen, Norway.ORCID 0000-0003-1184-3305
Helena U ZachariasPeter L. Reichertz Institute for Medical Informatics of TU Braunschweig and Hannover Medical School, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0003-3633-1330
Sushma Nagaraja GrellscheidComputational Biology Unit, Department of Biological Sciences, University of Bergen, N-5008 Bergen, Norway.ORCID 0000-0001-6410-1749
Michael AltenbuchingerDepartment of Medical Bioinformatics, University Medical Center Göttingen, 37075 Göttingen, Germany.ORCID 0000-0003-1102-6532

Funding

BMBF 01KD2208ADeutsche ForschungsgemeinschaftDFG 408885537Digital Tissue Deconvolution-Aus Einzelzelldaten lernen 420069742European Union's Horizon 2020 754688German Federal Ministry of Education and Research 01ZX1912AGerman Research Foundation AL 2355/1-1Trond Mohn Stiftelse BFS2017TMT01
6 · The paper itself

Abstract

motivationThe inference of cellular compositions from bulk and spatial transcriptomics data increasingly complements data analyses. Multiple computational approaches were suggested and recently, machine learning techniques were developed to systematically improve estimates. Such approaches allow to infer additional, less abundant cell types. However, they rely on training data which do not capture the full biological diversity encountered in transcriptomics analyses; data can contain cellular contributions not seen in the training data and as such, analyses can be biased or blurred. Thus, computational approaches have to deal with unknown, hidden contributions. Moreover, most methods are based on cellular archetypes which serve as a reference; e.g. a generic T-cell profile is used to infer the proportion of T-cells. It is well known that cells adapt their molecular phenotype to the environment and that pre-specified cell archetypes can distort the inference of cellular compositions.

resultsWe propose Adaptive Digital Tissue Deconvolution (ADTD) to estimate cellular proportions of pre-selected cell types together with possibly unknown and hidden background contributions. Moreover, ADTD adapts prototypic reference profiles to the molecular environment of the cells, which further resolves cell-type specific gene regulation from bulk transcriptomics data. We verify this in simulation studies and demonstrate that ADTD improves existing approaches in estimating cellular compositions. In an application to bulk transcriptomics data from breast cancer patients, we demonstrate that ADTD provides insights into cell-type specific molecular differences between breast cancer subtypes. AVAILABILITY AND IMPLEMENTATION: A python implementation of ADTD and a tutorial are available at Gitlab and zenodo (doi:10.5281/zenodo.7548362).

Indexed as

Machine LearningAlgorithmsBreast NeoplasmsComputational BiologyFemaleGene Expression ProfilingHumansTranscriptome

Identifiers

PMID38940181
PMCPMC11256946

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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.