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Torch-eCpG: A fast and scalable eQTM mapper for thousands of molecular phenotypes with graphical processing units.
Kober, Kord M; Berger, Liam; Roy, Ritu; Olshen, Adam.
Afiliação
  • Kober KM; School of Nursing, University of California San Francisco, San Francisco, California, USA.
  • Berger L; Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California, USA.
  • Roy R; Bakar Computational Health Sciences Institute, University of California San Francisco, San Francisco, California, USA.
  • Olshen A; School of Nursing, University of California San Francisco, San Francisco, California, USA.
bioRxiv ; 2023 Mar 10.
Article em En | MEDLINE | ID: mdl-36945384
ABSTRACT

Background:

Gene expression may be regulated by the DNA methylation of regulatory elements in cis, distal, and trans regions. One method to evaluate the relationship between DNA methylation and gene expression is the mapping of expression quantitative trait methylation (eQTM) loci (also called expression associated CpG loci, eCpG). However, no open-source tools are available to provide eQTM mapping. In addition, eQTM mapping can involve a large number of comparisons which may prevent the analyses due to limitations of computational resources. Here, we describe Torch-eCpG, an open-source tool to perform eQTM mapping that includes an optimized implementation that can use the graphical processing unit (GPU) to reduce runtime.

Results:

We demonstrate the analyses using the tool are reproducible, up to 18x faster using the GPU, and scale linearly with increasing methylation loci.

Conclusions:

Torch-eCpG is a fast, reliable, and scalable tool to perform eQTM mapping. Source code for Torch-eCpG is available at https//github.com/kordk/torch-ecpg.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2023 Tipo de documento: Article