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Towards molecular autopsies: Internal validation of the Qubit 1 X dsDNA HS Assay Kit

Molecular autopsies are post-mortem genetic analyses that can be used to aid in cause of death determination, especially in sudden unexpected death cases. Molecular autopsies involve analysing the decedent's DNA to identify potential pathogenic genetic variants. Accurate quantification of the DNA an...

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Main Author: Naidoo, Adele
Other Authors: Abrahams, Shameemah
Format: Thesis
Language:Eng
Published: Department of Pathology 2025
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access_status_str Open Access
author Naidoo, Adele
author2 Abrahams, Shameemah
author_browse Abrahams, Shameemah
Naidoo, Adele
author_facet Abrahams, Shameemah
Naidoo, Adele
author_sort Naidoo, Adele
collection Thesis
description Molecular autopsies are post-mortem genetic analyses that can be used to aid in cause of death determination, especially in sudden unexpected death cases. Molecular autopsies involve analysing the decedent's DNA to identify potential pathogenic genetic variants. Accurate quantification of the DNA and associated sequencing libraries is essential, however, no validation studies have been published on the recommended fluorometric quantification methods. The aim of this study was to internally validate the Qubit™ 1X dsDNA HS Assay Kit on the Qubit™ 4 Fluorometer as part of a molecular autopsy workflow for forensic applications. The Qubit™ 1X dsDNA HS Assay workflow was optimised and then used to assess the DNA concentration of control Lambda DNA, extracted DNA from forensic samples and DNA sequencing libraries. The accuracy, precision, dynamic range, and sensitivity were established in accordance with ISO 17025 standards. All parameters met the manufacturer's criteria of acceptance except for the precision of measurements for samples with DNA concentrations ≥ 0.5 ng/µl which were expected to be < 1% CV. The precision of the measurements (1.54% CV – 2.47 % CV), however, was deemed acceptable for our laboratory, as downstream DNA sequencing results surpassed quality thresholds. Additionally, DNA concentration measurements obtained from this DNA quantification workflow were similar to those obtained from other methods that have previously been validated in our laboratory. Overall, the Qubit™ 1X dsDNA HS Assay Kit was considered internally validated for DNA quantification in our laboratory and deemed fit for purpose. This study has enabled the use of this assay in the forensic setting for the first time and has advanced our progression towards implementing a molecular autopsy sequencing workflow in South Africa
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institution University of Cape Town (South Africa)
language Eng
last_indexed 2026-06-10T12:32:54.720Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2025
publishDateRange 2025
publishDateSort 2025
publisher Department of Pathology
publisherStr Department of Pathology
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source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/41175 Towards molecular autopsies: Internal validation of the Qubit 1 X dsDNA HS Assay Kit Naidoo, Adele Abrahams, Shameemah Pathology Molecular autopsies are post-mortem genetic analyses that can be used to aid in cause of death determination, especially in sudden unexpected death cases. Molecular autopsies involve analysing the decedent's DNA to identify potential pathogenic genetic variants. Accurate quantification of the DNA and associated sequencing libraries is essential, however, no validation studies have been published on the recommended fluorometric quantification methods. The aim of this study was to internally validate the Qubit™ 1X dsDNA HS Assay Kit on the Qubit™ 4 Fluorometer as part of a molecular autopsy workflow for forensic applications. The Qubit™ 1X dsDNA HS Assay workflow was optimised and then used to assess the DNA concentration of control Lambda DNA, extracted DNA from forensic samples and DNA sequencing libraries. The accuracy, precision, dynamic range, and sensitivity were established in accordance with ISO 17025 standards. All parameters met the manufacturer's criteria of acceptance except for the precision of measurements for samples with DNA concentrations ≥ 0.5 ng/µl which were expected to be < 1% CV. The precision of the measurements (1.54% CV – 2.47 % CV), however, was deemed acceptable for our laboratory, as downstream DNA sequencing results surpassed quality thresholds. Additionally, DNA concentration measurements obtained from this DNA quantification workflow were similar to those obtained from other methods that have previously been validated in our laboratory. Overall, the Qubit™ 1X dsDNA HS Assay Kit was considered internally validated for DNA quantification in our laboratory and deemed fit for purpose. This study has enabled the use of this assay in the forensic setting for the first time and has advanced our progression towards implementing a molecular autopsy sequencing workflow in South Africa 2025-03-13T12:50:44Z 2025-03-13T12:50:44Z 2024 2025-03-13T12:40:13Z Thesis / Dissertation Masters MPhil http://hdl.handle.net/11427/41175 Eng application/pdf Department of Pathology Faculty of Health Sciences University of Cape Town
spellingShingle Pathology
Naidoo, Adele
Towards molecular autopsies: Internal validation of the Qubit 1 X dsDNA HS Assay Kit
thesis_degree_str Master's
title Towards molecular autopsies: Internal validation of the Qubit 1 X dsDNA HS Assay Kit
title_full Towards molecular autopsies: Internal validation of the Qubit 1 X dsDNA HS Assay Kit
title_fullStr Towards molecular autopsies: Internal validation of the Qubit 1 X dsDNA HS Assay Kit
title_full_unstemmed Towards molecular autopsies: Internal validation of the Qubit 1 X dsDNA HS Assay Kit
title_short Towards molecular autopsies: Internal validation of the Qubit 1 X dsDNA HS Assay Kit
title_sort towards molecular autopsies internal validation of the qubit 1 x dsdna hs assay kit
topic Pathology
url http://hdl.handle.net/11427/41175
work_keys_str_mv AT naidooadele towardsmolecularautopsiesinternalvalidationofthequbit1xdsdnahsassaykit