Predicting cell population-specific gene expression from genomic sequence
Frontiers in Bioinformatics, vol. 4, pp. 1347276
Abstract
Most regulatory elements, especially enhancer sequences, are cell population-specific. One could even argue that a distinct set of regulatory elements is what defines a cell population. However, discovering which non-coding regions of the DNA are essential in which context, and as a result, which genes are expressed, is a difficult task. Some computational models tackle this problem by predicting gene expression directly from the genomic sequence. These models are currently limited to predicting bulk measurements and mainly make tissue-specific predictions. Here, we present a model that leverages single-cell RNA-sequencing data to predict gene expression. We show that cell population-specific models outperform tissue-specific models, especially when the expression profile of a cell population and the corresponding tissue are dissimilar. Further, we show that our model can prioritize GWAS variants and learn motifs of transcription factor binding sites. We envision that our model can be useful for delineating cell population-specific regulatory elements.
Authors 3
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Lieke Michielsen Aachen Department of Human Genetics Leiden Computational Biology Center Leiden Computational Biology Centre
Leiden University · Leiden University Medical Center · Delft University of Technology
Affiliation as printed
Delft Bioinformatics Lab, Delft University of Technology, Delft, Netherlands
Department of Human Genetics, Leiden University Medical Center, Leiden, Netherlands
Leiden Computational Biology Center, Leiden University Medical Center, Leiden, Netherlands
Delft Bioinformatics Lab, Netherlands
Department of Human Genetics, Netherlands
Leiden Computational Biology Center, Netherlands
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Marcel J. T. Reinders Aachen Department of Human Genetics Leiden Computational Biology Center Leiden Computational Biology Centre
Leiden University · Leiden University Medical Center · Delft University of Technology
Affiliation as printed
Delft Bioinformatics Lab, Delft University of Technology, Delft, Netherlands
Department of Human Genetics, Leiden University Medical Center, Leiden, Netherlands
Leiden Computational Biology Center, Leiden University Medical Center, Leiden, Netherlands
Delft Bioinformatics Lab, Netherlands
Department of Human Genetics, Netherlands
Leiden Computational Biology Center, Netherlands
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Ahmed Essam Mahfouz corresponding Aachen Department of Human Genetics Leiden Computational Biology Center Leiden Computational Biology Centre
Leiden University · Leiden University Medical Center · Delft University of Technology
Affiliation as printed
Delft Bioinformatics Lab, Delft University of Technology, Delft, Netherlands
Department of Human Genetics, Leiden University Medical Center, Leiden, Netherlands
Leiden Computational Biology Center, Leiden University Medical Center, Leiden, Netherlands
Delft Bioinformatics Lab, Netherlands
Department of Human Genetics, Netherlands
Leiden Computational Biology Center, Netherlands
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