Genomic Variations Explorer (GenVarX): a toolset for annotating promoter and CNV regions using genotypic and phenotypic differences

Frontiers in Genetics

Genetics

Jana Biová¹  Mária Škrabišová¹  Nicholas Dietz²  Anser Mahmood²  Kristin Bilyeu³  Yen On Chan⁴  Trupti Joshi⁵ 

[1] Department of Biochemistry, Faculty of Science, Palacky University in Olomouc, Olomouc, Czechia;Division of Plant Science and Technology, University of Missouri-Columbia, Columbia, MO, United States;Division of Plant Science and Technology, University of Missouri-Columbia, Columbia, MO, United States;Plant Genetics Research Unit, United States Department of Agriculture-Agricultural Research Service, Columbia, MO, United States;MU Institute for Data Science and Informatics, University of Missouri-Columbia, Columbia, MO, United States;MU Institute for Data Science and Informatics, University of Missouri-Columbia, Columbia, MO, United States;Christopher S. Bond Life Sciences Center, University of Missouri-Columbia, Columbia, MO, United States;Department of Electrical Engineering and Computer Science, University of Missouri-Columbia, Columbia, MO, United States;Department of Biomedical Informatics, Biostatistics and Medical Epidemiology, University of Missouri-Columbia, Columbia, MO, United States;

关键词: transcription factor;    promoter;    copy number variation;    whole genome re-sequencing data;    genomic variations;    SNPs;    Indels;    phenotypes;   

DOI  :  10.3389/fgene.2023.1251382

 received in 2023-07-01, accepted in 2023-09-27,  发布年份 2023

来源: Frontiers

【 摘 要 】

The rapid growth of sequencing technology and its increasing popularity in biology-related research over the years has made whole genome re-sequencing (WGRS) data become widely available. A large amount of WGRS data can unlock the knowledge gap between genomics and phenomics through gaining an understanding of the genomic variations that can lead to phenotype changes. These genomic variations are usually comprised of allele and structural changes in DNA, and these changes can affect the regulatory mechanisms causing changes in gene expression and altering the phenotypes of organisms. In this research work, we created the GenVarX toolset, that is backed by transcription factor binding sequence data in promoter regions, the copy number variations data, SNPs and Indels data, and phenotypes data which can potentially provide insights about phenotypic differences and solve compelling questions in plant research. Analytics-wise, we have developed strategies to better utilize the WGRS data and mine the data using efficient data processing scripts, libraries, tools, and frameworks to create the interactive and visualization-enhanced GenVarX toolset that encompasses both promoter regions and copy number variation analysis components. The main capabilities of the GenVarX toolset are to provide easy-to-use interfaces for users to perform queries, visualize data, and interact with the data. Based on different input windows on the user interface, users can provide inputs corresponding to each field and submit the information as a query. The data returned on the results page is usually displayed in a tabular fashion. In addition, interactive figures are also included in the toolset to facilitate the visualization of statistical results or tool outputs. Currently, the GenVarX toolset supports soybean, rice, and Arabidopsis. The researchers can access the soybean GenVarX toolset from SoyKB via https://soykb.org/SoybeanGenVarX/, rice GenVarX toolset, and Arabidopsis GenVarX toolset from KBCommons web portal with links https://kbcommons.org/system/tools/GenVarX/Osativa and https://kbcommons.org/system/tools/GenVarX/Athaliana, respectively.

【 授权许可】

Unknown   
Copyright © 2023 Chan, Biová, Mahmood, Dietz, Bilyeu, Škrabišová and Joshi.