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Elucidation of transcriptional regul...
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Jin, Jiaqi.
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Elucidation of transcriptional regulation by analyzing Next-Generation Sequencing data.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Elucidation of transcriptional regulation by analyzing Next-Generation Sequencing data./
作者:
Jin, Jiaqi.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2016,
面頁冊數:
214 p.
附註:
Source: Dissertation Abstracts International, Volume: 77-12(E), Section: B.
Contained By:
Dissertation Abstracts International77-12B(E).
標題:
Genetics. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10155152
ISBN:
9781369102376
Elucidation of transcriptional regulation by analyzing Next-Generation Sequencing data.
Jin, Jiaqi.
Elucidation of transcriptional regulation by analyzing Next-Generation Sequencing data.
- Ann Arbor : ProQuest Dissertations & Theses, 2016 - 214 p.
Source: Dissertation Abstracts International, Volume: 77-12(E), Section: B.
Thesis (Ph.D.)--Yale University, 2016.
The advancements in the Next-Generation Sequencing (NGS) technology have enabled researchers to study complex genomic questions at the whole genome level. At the same time, the unprecedented massive data generated from NGS experiments poses serious challenges in data analysis and interpretation. One of the most intriguing questions in genomics is how gene transcription is regulated by different elements, such as transcription factors (TFs), histone modifications and DNA methylation. My research primarily focused on analyzing, interpreting and integrating different NGS data sets to understand transcriptional regulation by distinct genomic elements and the associated biological significances in various scenarios.
ISBN: 9781369102376Subjects--Topical Terms:
530508
Genetics.
Elucidation of transcriptional regulation by analyzing Next-Generation Sequencing data.
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The advancements in the Next-Generation Sequencing (NGS) technology have enabled researchers to study complex genomic questions at the whole genome level. At the same time, the unprecedented massive data generated from NGS experiments poses serious challenges in data analysis and interpretation. One of the most intriguing questions in genomics is how gene transcription is regulated by different elements, such as transcription factors (TFs), histone modifications and DNA methylation. My research primarily focused on analyzing, interpreting and integrating different NGS data sets to understand transcriptional regulation by distinct genomic elements and the associated biological significances in various scenarios.
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The first chapter briefly overviews the molecular mechanisms of transcriptional regulation by TFs, histone modifications and DNA methylation.
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In the second chapter, we address the problem of peak detection in ChIP-seq experiments for TFs. Numerous algorithms have been developed to detect TF binding sites from ChIP-seq data. However all of these algorithms have several shortcomings, including requirement for matched negative controls and susceptibility to false positives (artifacts). We present Ritornello, a novel control-free and high-fidelity peak calling algorithm we developed for TF binding sites detection.
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In the third chapter, we study the role of BCOR as a subunit of a non-canonical PRC1 in repressing the transcription of genes associated with differentiation in human Embryonic Stem Cells (hESCs). We identify the direct gene targets repressed by BCOR and establish the requirement for BCOR in hESC maintenance.
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