Detect inosine using nanopore sequencing

Adenosine to Inosine (A-to-I) editing is one of the most prevalent post-transcriptional RNA modifications. It plays numerous crucial roles in determining a cell's fate. Until now, there is no direct approach to detect Inosine in RNA yet. Here, we introduce a method to detect Inosine using Nanop...

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Main Author: Nguyen, Tram Anh
Other Authors: Tan Meng How
Format: Final Year Project
Language:English
Published: Nanyang Technological University 2021
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Online Access:https://hdl.handle.net/10356/151918
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1519182021-07-09T12:08:02Z Detect inosine using nanopore sequencing Nguyen, Tram Anh Tan Meng How School of Chemical and Biomedical Engineering mh.tan@ntu.edu.sg Engineering::Bioengineering Adenosine to Inosine (A-to-I) editing is one of the most prevalent post-transcriptional RNA modifications. It plays numerous crucial roles in determining a cell's fate. Until now, there is no direct approach to detect Inosine in RNA yet. Here, we introduce a method to detect Inosine using Nanopore direct RNA sequencing with high overall accuracy and area under the curve (AUC) of receiver operating characteristic (ROC) and precision-recall (PR) around 90%. Our method is based on the differences in current signal, as well as base-calling and alignment errors from Inosine. We also explored that the sequence context goes beyond the widely used 5-mer in Nanopore. A series of convolutional neural networks (CNN) was built to detect Inosine from not only Adenosine but also single nucleotide polymorphism (SNP). We then show that our method can be generalized to identify edit sites from unseen organisms. Our result will shed light on the future of investigating more about RNA modifications and their roles in the cells. Bachelor of Engineering (Bioengineering) 2021-07-08T00:29:46Z 2021-07-08T00:29:46Z 2021 Final Year Project (FYP) Nguyen, T. A. (2021). Detect inosine using nanopore sequencing. Final Year Project (FYP), Nanyang Technological University, Singapore. https://hdl.handle.net/10356/151918 https://hdl.handle.net/10356/151918 en application/pdf Nanyang Technological University
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Bioengineering
spellingShingle Engineering::Bioengineering
Nguyen, Tram Anh
Detect inosine using nanopore sequencing
description Adenosine to Inosine (A-to-I) editing is one of the most prevalent post-transcriptional RNA modifications. It plays numerous crucial roles in determining a cell's fate. Until now, there is no direct approach to detect Inosine in RNA yet. Here, we introduce a method to detect Inosine using Nanopore direct RNA sequencing with high overall accuracy and area under the curve (AUC) of receiver operating characteristic (ROC) and precision-recall (PR) around 90%. Our method is based on the differences in current signal, as well as base-calling and alignment errors from Inosine. We also explored that the sequence context goes beyond the widely used 5-mer in Nanopore. A series of convolutional neural networks (CNN) was built to detect Inosine from not only Adenosine but also single nucleotide polymorphism (SNP). We then show that our method can be generalized to identify edit sites from unseen organisms. Our result will shed light on the future of investigating more about RNA modifications and their roles in the cells.
author2 Tan Meng How
author_facet Tan Meng How
Nguyen, Tram Anh
format Final Year Project
author Nguyen, Tram Anh
author_sort Nguyen, Tram Anh
title Detect inosine using nanopore sequencing
title_short Detect inosine using nanopore sequencing
title_full Detect inosine using nanopore sequencing
title_fullStr Detect inosine using nanopore sequencing
title_full_unstemmed Detect inosine using nanopore sequencing
title_sort detect inosine using nanopore sequencing
publisher Nanyang Technological University
publishDate 2021
url https://hdl.handle.net/10356/151918
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