DEVELOPMENTS TOWARDS SINGLE MOLECULE AND SINGLE CELL GENETIC AND EPIGENETIC ANALYSIS TECHNOLOGIES

New discoveries in the realm of biology often come hand-in-hand with innovations in technology. Over the last two decades, advancements in microfabrication and microscopy have opened biological phenomena to be studied in fundamental units rather than as a collective entity. From these efforts, the axioms upon which we built our fundamental concepts in anatomy and physiology have been reshaped. We now understand that even within a subpopulation of cells taken from the same tissue, cell-to-cell variations exist in both phenotypic and genotypic expression. These variations are found to play critical roles in disease state and progression, thus, research into single cells and single molecules are a necessity to improving treatment. In this work, methods of single molecule analysis of native human chromatin fibers are presented as well as methods and devices for multi- and single cell genome analysis. As the handling of single molecules and single cells are facilitated by microfabricated devices, discussed herein are their designs, fabrication methods, operational procedures, working principles, and experimental results representative of their biologically relevant impact. Our findings point towards potential platform technologies in high-throughput chromatin linearization for fluorescence based epigenetic mapping and single cell whole genome amplification with reduced amplification bias and improved genome coverage.

Name thesis:degree_name

Ph. D., Biomedical Engineering

Level thesis:degree_level

Doctor of Philosophy

Discipline thesis:degree_discipline

Biomedical Engineering

Grantor

Cornell University

Year dc:date.issued

2017

Author dc:creator

• Tian, Harvey Chen

Committee members dc:contributor.committeemember

• Luo, Dan
• Zipfel, Warren R

• Amplification
• DNA
• Microfluidic
• Micropillar
• Sequencing
• Single Cell
• Genetics
• Biomedical engineering

Language dc:language.iso

en_US

DOI

https://doi.org/10.7298/X4DJ5CRT

Dc Identifier Other

ProQuest Submission ID: 10206
ProQuest Publication ID: 10258101

OAI identifier oai:identifier

oai:ecommons.cornell.edu:1813/51584