Evidence map›Paper›PMID 31504167›Full record

ArticleBioinformatics (Oxford, England)2020

Regulatory annotation of genomic intervals based on tissue-specific expression QTLs.

Tianlei Xu, Peng Jin, Zhaohui S Qin

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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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.

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3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

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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

3 authors.

Tianlei XuDepartment of Mathematics and Computer Science, Emory University, Atlanta, GA 30322, USA.
Peng JinDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.
Zhaohui S QinDepartment of Biostatics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA 30322, USA.

Funding

Computational Prediction and Functional Validation of Novel Epigenetic Risk Loci in Alzheimer's DiseaseR56AG062256 · NIA · EMORY UNIVERSITY · PI JIN, PENG, QIN, ZHAOHUI · 2018 to 2018
$788k
Computational Prediction and Functional Validation of Novel Risk Loci of Alzheimer's DiseaseR56AG060757 · NIA · EMORY UNIVERSITY · PI JIN, PENG, QIN, ZHAOHUI · 2018 to 2018
$788k
NIA NIH HHS R56 AG060757NIA NIH HHS R56 AG062256
6 · The paper itself

Abstract

motivationAnnotating a given genomic locus or a set of genomic loci is an important yet challenging task. This is especially true for the non-coding part of the genome which is enormous yet poorly understood. Since gene set enrichment analyses have demonstrated to be effective approach to annotate a set of genes, the same idea can be extended to explore the enrichment of functional elements or features in a set of genomic intervals to reveal potential functional connections.

resultsIn this study, we describe a novel computational strategy named loci2path that takes advantage of the newly emerged, genome-wide and tissue-specific expression quantitative trait loci (eQTL) information to help annotate a set of genomic intervals in terms of transcription regulation. By checking the presence or the absence of millions of eQTLs in a set of input genomic intervals, combined with grouping eQTLs by the pathways or gene sets that their target genes belong to, loci2path build a bridge connecting genomic intervals to functional pathways and pre-defined biological-meaningful gene sets, revealing potential for regulatory connection. Our method enjoys two key advantages over existing methods: first, we no longer rely on proximity to link a locus to a gene which has shown to be unreliable; second, eQTL allows us to provide the regulatory annotation under the context of specific tissue types. To demonstrate its utilities, we apply loci2path on sets of genomic intervals harboring disease-associated variants as query. Using 1 702 612 eQTLs discovered by the Genotype-Tissue Expression (GTEx) project across 44 tissues and 6320 pathways or gene sets cataloged in MSigDB as annotation resource, our method successfully identifies highly relevant biological pathways and revealed disease mechanisms for psoriasis and other immune-related diseases. Tissue specificity analysis of associated eQTLs provide additional evidence of the distinct roles of different tissues played in the disease mechanisms. AVAILABILITY AND IMPLEMENTATION: loci2path is published as an open source Bioconductor package, and it is available at http://bioconductor.org/packages/release/bioc/html/loci2path.html. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

GenomicsQuantitative Trait LociGene Expression RegulationGenome-Wide Association StudyOrgan SpecificityPolymorphism, Single Nucleotide

Identifiers

PMID31504167
PMCPMC8215915

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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.