Publications by authors named "Xiavan Roopnarinesingh"

Article Synopsis
  • The study aimed to uncover additional DNA methylation changes in lupus T cells, focusing on the link between genetic factors and epigenetic alterations.
  • Researchers analyzed DNA methylation patterns in T cells from 74 lupus patients compared to healthy controls, using extensive sampling and meQTL analysis to understand genetic influences.
  • The findings confirmed hypomethylation in interferon-regulated genes and identified changes in the miR-17-92 cluster, which are correlated with disease activity, but concluded that genetic factors minimally contribute to the observed epigenetic changes associated with lupus.
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Background Transcriptional correlation networks derived from publicly available gene expression microarrays have been previously shown to be predictive of known gene functions, but less is known about the predictive capacity of correlated DNA methylation at CpG sites. Guilt-by-association co-expression methods can adapted for use with DNA methylation when a representative methylation value is created for each gene. We examine how methylation compares to expression in predicting Gene Ontology terms using both co-methylation and traditional machine learning approaches across different types of representative methylation values per gene.

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Epigenetic alterations are a hallmark of aging and age-related diseases. Computational models using DNA methylation data can create "epigenetic clocks" which are proposed to reflect "biological" aging. Thus, it is important to understand the relationship between predictive clock sites and aging biology.

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Background: The number of publicly available metagenomic experiments in various environments has been rapidly growing, empowering the potential to identify similar shifts in species abundance between different experiments. This could be a potentially powerful way to interpret new experiments, by identifying common themes and causes behind changes in species abundance.

Results: We propose a novel framework for comparing microbial shifts between conditions.

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Background: NCBI's Gene Expression Omnibus (GEO) is a rich community resource containing millions of gene expression experiments from human, mouse, rat, and other model organisms. However, information about each experiment (metadata) is in the format of an open-ended, non-standardized textual description provided by the depositor. Thus, classification of experiments for meta-analysis by factors such as gender, age of the sample donor, and tissue of origin is not feasible without assigning labels to the experiments.

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