Evidence map›Paper›PMID 39230700›Full record

ArticleBioinformatics (Oxford, England)2024

Metadata-guided feature disentanglement for functional genomics.

Alexander Rakowski, Remo Monti, Viktoriia Huryn, Marta Lemanczyk, Uwe Ohler, Christoph Lippert

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 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. 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.

Alexander RakowskiDigital Health Machine Learning, Hasso Plattner Institute for Digital Engineering, Digital Engineering, University of Potsdam, Campus III Building G2, Rudolf-Breitscheid-Strasse 187, Potsdam, Brandenburg, 14482, Germany.
Remo MontiDigital Health Machine Learning, Hasso Plattner Institute for Digital Engineering, Digital Engineering, University of Potsdam, Campus III Building G2, Rudolf-Breitscheid-Strasse 187, Potsdam, Brandenburg, 14482, Germany.
Viktoriia HurynMax-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin Institute for Medical Systems Biology, Department of Biology, Humboldt Universität Berlin, Hannoversche Strasse 28, Building 101, Room 1.05, Berlin, 10115, Germany.
Marta LemanczykData Analytics and Computational Statistics, Hasso Plattner Institute for Digital Engineering, Digital Engineering, University of Potsdam, Potsdam, Brandenburg, 14482, Germany.
Uwe OhlerMax-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin Institute for Medical Systems Biology, Department of Biology, Humboldt Universität Berlin, Hannoversche Strasse 28, Building 101, Room 1.05, Berlin, 10115, Germany.
Christoph LippertDigital Health Machine Learning, Hasso Plattner Institute for Digital Engineering, Digital Engineering, University of Potsdam, Campus III Building G2, Rudolf-Breitscheid-Strasse 187, Potsdam, Brandenburg, 14482, Germany.

Funding

Deutsche Forschungsgemeinschaft LI 3333/5-1European Commission 101016775Helmholtz Einstein International Berlin Research School in Data ScienceHPI Research School on Data Science and Engineering
6 · The paper itself

Abstract

With the development of high-throughput technologies, genomics datasets rapidly grow in size, including functional genomics data. This has allowed the training of large Deep Learning (DL) models to predict epigenetic readouts, such as protein binding or histone modifications, from genome sequences. However, large dataset sizes come at a price of data consistency, often aggregating results from a large number of studies, conducted under varying experimental conditions. While data from large-scale consortia are useful as they allow studying the effects of different biological conditions, they can also contain unwanted biases from confounding experimental factors. Here, we introduce Metadata-guided Feature Disentanglement (MFD)-an approach that allows disentangling biologically relevant features from potential technical biases. MFD incorporates target metadata into model training, by conditioning weights of the model output layer on different experimental factors. It then separates the factors into disjoint groups and enforces independence of the corresponding feature subspaces with an adversarially learned penalty. We show that the metadata-driven disentanglement approach allows for better model introspection, by connecting latent features to experimental factors, without compromising, or even improving performance in downstream tasks, such as enhancer prediction, or genetic variant discovery. The code will be made available at https://github.com/HealthML/MFD.

Indexed as

GenomicsMetadataDeep LearningHumans

Identifiers

PMID39230700
PMCPMC11373386

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.