Jiang, Yan
(2019)
Estimating DNA methylation levels for single-cell bisulfite sequencing (BS-SEQ) data.
Master's Thesis, University of Pittsburgh.
(Unpublished)
Abstract
DNA methylation is among the most studied epigenetic marks, with essential influence on biological growths, disease developments and potential public health benefits. Modified from the well-established measuring method bisulfite sequencing (BS-seq), single-cell bisulfite sequencing (scBS-seq) emerged recently to identify DNA methylation status within a single cell to profile and study heterogeneities better. With the unique features of the single-cell DNA methylation data, there is in need of developing a new method to assign the methylation status for each CpG site more accurately and precisely to represent the underlying truth. In this study, we propose a method using Bayes rule and compare its performance with a simple one-third rule method. A simulation study with various settings is conducted to compare the accuracy, precision and bias. The Bayes’ method shows an improvement in dimensions of accuracy and bias.
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Details
Item Type: |
University of Pittsburgh ETD
|
Status: |
Unpublished |
Creators/Authors: |
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ETD Committee: |
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Date: |
25 June 2019 |
Date Type: |
Publication |
Defense Date: |
12 April 2019 |
Approval Date: |
25 June 2019 |
Submission Date: |
4 April 2019 |
Access Restriction: |
No restriction; Release the ETD for access worldwide immediately. |
Number of Pages: |
26 |
Institution: |
University of Pittsburgh |
Schools and Programs: |
School of Public Health > Biostatistics |
Degree: |
MS - Master of Science |
Thesis Type: |
Master's Thesis |
Refereed: |
Yes |
Uncontrolled Keywords: |
DNA methylation; single-cell bisulfite sequencing (scBS-seq); Bayes’ rule |
Date Deposited: |
25 Jun 2019 14:40 |
Last Modified: |
25 Jun 2019 14:40 |
URI: |
http://d-scholarship.pitt.edu/id/eprint/36276 |
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