Using high-throughput sequencing data to identify the transcriptional start sites of mouse microRNAs

碩士 === 國立中興大學 === 基因體暨生物資訊學研究所 === 101 === MicroRNAs (miRNAs) are non-coding small RNAs that inhibit protein coding gene expression by hybridizing with messenger RNAs (mRNAs). MiRNAs are involved in a lot of diverse biological processes and various diseases. To identify miRNA transcription start sit...

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Main Authors: Hao-Yu Fang, 方浩宇
Other Authors: 謝立青
Format: Others
Language:zh-TW
Published: 2013
Online Access:http://ndltd.ncl.edu.tw/handle/32453885381096374336
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spelling ndltd-TW-101NCHU51050892017-10-29T04:34:20Z http://ndltd.ncl.edu.tw/handle/32453885381096374336 Using high-throughput sequencing data to identify the transcriptional start sites of mouse microRNAs 利用高通量定序資料預測老鼠微核醣核酸轉錄起始位置 Hao-Yu Fang 方浩宇 碩士 國立中興大學 基因體暨生物資訊學研究所 101 MicroRNAs (miRNAs) are non-coding small RNAs that inhibit protein coding gene expression by hybridizing with messenger RNAs (mRNAs). MiRNAs are involved in a lot of diverse biological processes and various diseases. To identify miRNA transcription start sites (TSSs) is important for studying the upstream regulatory networks of miRNAs. Up to now the studies regarding miRNA TSS identification are all focus on human miRNAs. We are interested in other species and our aim in this study is to identify mouse miRNA TSSs and the result would contribute to understanding the evolution of upstream regulatory networks of miRNAs. In this study, we integrated two types of high-throughput sequencing data, i.e. transcription start sites sequencing (TSSseq) and Cap Analysis of Gene Expression (CAGE), as the evidence of miRNA TSSs. A machine-learning-based Support Vector Machine (SVM) was developed to identify mouse miRNA TSSs. In addition, we also incorporated the ESTs (expression sequence tag) and sequence conservation information to provide evidence for mouse miRNA TSSs. 謝立青 2013 學位論文 ; thesis 44 zh-TW
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language zh-TW
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description 碩士 === 國立中興大學 === 基因體暨生物資訊學研究所 === 101 === MicroRNAs (miRNAs) are non-coding small RNAs that inhibit protein coding gene expression by hybridizing with messenger RNAs (mRNAs). MiRNAs are involved in a lot of diverse biological processes and various diseases. To identify miRNA transcription start sites (TSSs) is important for studying the upstream regulatory networks of miRNAs. Up to now the studies regarding miRNA TSS identification are all focus on human miRNAs. We are interested in other species and our aim in this study is to identify mouse miRNA TSSs and the result would contribute to understanding the evolution of upstream regulatory networks of miRNAs. In this study, we integrated two types of high-throughput sequencing data, i.e. transcription start sites sequencing (TSSseq) and Cap Analysis of Gene Expression (CAGE), as the evidence of miRNA TSSs. A machine-learning-based Support Vector Machine (SVM) was developed to identify mouse miRNA TSSs. In addition, we also incorporated the ESTs (expression sequence tag) and sequence conservation information to provide evidence for mouse miRNA TSSs.
author2 謝立青
author_facet 謝立青
Hao-Yu Fang
方浩宇
author Hao-Yu Fang
方浩宇
spellingShingle Hao-Yu Fang
方浩宇
Using high-throughput sequencing data to identify the transcriptional start sites of mouse microRNAs
author_sort Hao-Yu Fang
title Using high-throughput sequencing data to identify the transcriptional start sites of mouse microRNAs
title_short Using high-throughput sequencing data to identify the transcriptional start sites of mouse microRNAs
title_full Using high-throughput sequencing data to identify the transcriptional start sites of mouse microRNAs
title_fullStr Using high-throughput sequencing data to identify the transcriptional start sites of mouse microRNAs
title_full_unstemmed Using high-throughput sequencing data to identify the transcriptional start sites of mouse microRNAs
title_sort using high-throughput sequencing data to identify the transcriptional start sites of mouse micrornas
publishDate 2013
url http://ndltd.ncl.edu.tw/handle/32453885381096374336
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