Authors
Roy, Christian K.Faculty Advisor
Melissa J. Moore, PhD; Phillip D. Zamore, PhDAcademic Program
Biochemistry and Molecular PharmacologyUMass Chan Affiliations
RNA Therapeutics InstituteDocument Type
Doctoral DissertationPublication Date
2014-05-21Keywords
Dissertations, UMMSDNA
Gene Expression
Gene Expression Profiling
High-Throughput Nucleotide Sequencing
Protein Isoforms
RNA
RNA, Small Interfering
Sequence Analysis, DNA
Transcriptome
DNA
Gene Expression
Gene Expression Profiling
High-Throughput Nucleotide Sequencing
Protein Isoforms
RNA
Small Interfering RNA
DNA Sequence Analysis
Transcriptome
Biochemistry
Bioinformatics
Computational Biology
Genetics
Genomics
Systems Biology
Metadata
Show full item recordAbstract
Analysis of gene expression has undergone a technological revolution. What was impossible 6 years ago is now routine. High-throughput DNA sequencing machines capable of generating hundreds of millions of reads allow, indeed force, a major revision toward the study of the genome’s functional output—the transcriptome. This thesis examines the history of DNA sequencing, measurement of gene expression by sequencing, isoform complexity driven by alternative splicing and mammalian piRNA precursor biogenesis. Examination of these topics is framed around development of a novel RNA-templated DNA-DNA ligation assay (SeqZip) that allows for efficient analysis of abundant, complex, and functional long RNAs. The discussion focuses on the future of transcriptome analysis, development and applications of SeqZip, and challenges presented to biomedical researchers by extremely large and rich datasets.DOI
10.13028/M2X60KPermanent Link to this Item
http://hdl.handle.net/20.500.14038/32086Rights
Copyright is held by the author, with all rights reserved.ae974a485f413a2113503eed53cd6c53
10.13028/M2X60K