Statistical Analysis of Quantitative PCR Data

This thesis seeks to develop a better understanding of the analysis of gene expression to find the amount of transcript in a sample. The mainstream method used is called Polymerase Chain Reaction (PCR) and it exploits the DNA's ability to replicate. The comparative CT method estimate the starti...

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Main Author: Lien, Tonje Gulbrandsen
Format: Others
Language:English
Published: Norges teknisk-naturvitenskapelige universitet, Institutt for matematiske fag 2011
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Online Access:http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-13094
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spelling ndltd-UPSALLA1-oai-DiVA.org-ntnu-130942013-01-08T13:32:16ZStatistical Analysis of Quantitative PCR DataengLien, Tonje GulbrandsenNorges teknisk-naturvitenskapelige universitet, Institutt for matematiske fagInstitutt for matematiske fag2011ntnudaim:6159MTFYMA fysikk og matematikkIndustriell matematikkThis thesis seeks to develop a better understanding of the analysis of gene expression to find the amount of transcript in a sample. The mainstream method used is called Polymerase Chain Reaction (PCR) and it exploits the DNA's ability to replicate. The comparative CT method estimate the starting fluorescence level f0 by assuming constant amplification in each PCR cycle, and it uses the fluorescence level which has risen above a certain threshold. We present a generalization of this method, where different threshold values can be used. The main aim of this thesis is to evaluate a new method called the Enzymological method. It estimates f0 by considering a cycle dependent amplification and uses a larger part of the fluorescence curves, than the two CT methods. All methods are tested on dilution series, where the dilution factors are known. In one of the datasets studied, the Clusterin dilution-dataset, we get better estimates from the Enzymological method compared to the two CT methods. Student thesisinfo:eu-repo/semantics/bachelorThesistexthttp://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-13094Local ntnudaim:6159application/pdfinfo:eu-repo/semantics/openAccess
collection NDLTD
language English
format Others
sources NDLTD
topic ntnudaim:6159
MTFYMA fysikk og matematikk
Industriell matematikk
spellingShingle ntnudaim:6159
MTFYMA fysikk og matematikk
Industriell matematikk
Lien, Tonje Gulbrandsen
Statistical Analysis of Quantitative PCR Data
description This thesis seeks to develop a better understanding of the analysis of gene expression to find the amount of transcript in a sample. The mainstream method used is called Polymerase Chain Reaction (PCR) and it exploits the DNA's ability to replicate. The comparative CT method estimate the starting fluorescence level f0 by assuming constant amplification in each PCR cycle, and it uses the fluorescence level which has risen above a certain threshold. We present a generalization of this method, where different threshold values can be used. The main aim of this thesis is to evaluate a new method called the Enzymological method. It estimates f0 by considering a cycle dependent amplification and uses a larger part of the fluorescence curves, than the two CT methods. All methods are tested on dilution series, where the dilution factors are known. In one of the datasets studied, the Clusterin dilution-dataset, we get better estimates from the Enzymological method compared to the two CT methods.
author Lien, Tonje Gulbrandsen
author_facet Lien, Tonje Gulbrandsen
author_sort Lien, Tonje Gulbrandsen
title Statistical Analysis of Quantitative PCR Data
title_short Statistical Analysis of Quantitative PCR Data
title_full Statistical Analysis of Quantitative PCR Data
title_fullStr Statistical Analysis of Quantitative PCR Data
title_full_unstemmed Statistical Analysis of Quantitative PCR Data
title_sort statistical analysis of quantitative pcr data
publisher Norges teknisk-naturvitenskapelige universitet, Institutt for matematiske fag
publishDate 2011
url http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-13094
work_keys_str_mv AT lientonjegulbrandsen statisticalanalysisofquantitativepcrdata
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