Expanding the frontiers of transcriptome sequencing data (RNA-seq): selection signatures in chickens

Author(s)Adetunji, Modupeore O.
Date Accessioned2020-01-10T14:22:23Z
Date Available2020-01-10T14:22:23Z
Publication Date2019
SWORD Update2019-07-13T16:03:19Z
AbstractTranscriptome sequencing (RNA-seq) analysis is a highly exploited technique for defining transcript abundance and differential expression analysis but is underutilized for nucleotide variant detection. Given the ability of RNA-seq to reveal active regions of the genome, detection of RNA-seq SNPs can prove valuable in understanding the phenotypic diversity between populations. This dissertation showcases the applicability of RNA-seq data in currently unexplored but important areas of biological research; such as variant analysis and detection of selection signatures in commercial broilers. I have developed a novel computational workflow that takes advantage of multiple RNA-seq splice aware aligners to call SNPs using RNA-seq data only. Our workflow achieved high precision and sensitivity, furthermore, we discovered SNPs resulting from post-translational events that would have been missed in WGS data. The results demonstrate SNP identification from RNA-seq data be reliable and a potential resource in determining selection signatures from variants. The identification of regions that have undergone selection is important in understanding the variation patterns responsible for the underlying phenotypic changes between populations. Modern broilers are characterized from decades of extensive genetic selection for traits of economic importance. However, improvement in economic traits also resulted in negative complications, such as skeletal abnormalities, inability to adapt to heat stress and susceptibility to diseases. These phenotypic changes imply strong positive selection for the causal loci or polymorphisms controlling these traits. To offer insight into the variation patterns responsible for the underlying phenotypic changes, we investigated regions of selection using the SNPs derived from our RNA-seq workflow in commercial broilers. ☐ Given the vast amounts of data generated by next-generation sequencing (NGS) data for the today’s -omics era, the ability to efficiently manage the massive throughput from NGS analysis becomes a major challenge, especially when dealing with data that range on a terabyte to petabyte scale. Thus, innovative storage solutions that address this computational bottleneck are paramount. To this aim, we designed a hybrid (Relational & NoSQL) database framework, called TransAtlasDB, that addresses the crucial need for a smart and innovative storage solution for management and retrieval of large-scale transcriptomics data output relevant to basic, medical and agriculture research.en_US
AdvisorSchmidt, Carl J.
DegreePh.D.
DepartmentUniversity of Delaware, Center for Bioinformatics and Computational Biology
DepartmentUniversity of Delaware, Department of Animal and Food Sciences
DOIhttps://doi.org/10.58088/b1hm-hx82
Unique Identifier1135485290
URLhttp://udspace.udel.edu/handle/19716/24934
Languageen
PublisherUniversity of Delawareen_US
URIhttps://search.proquest.com/docview/2284204796?accountid=10457
TitleExpanding the frontiers of transcriptome sequencing data (RNA-seq): selection signatures in chickensen_US
TypeThesisen_US
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