The Application of Modern Statistical Methods to the Advance of Probabilistic Genotyping

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dc.contributor.advisor Curran, James M.
dc.contributor.advisor Buckleton, John B.
dc.contributor.author Cheng, Kae-Wen (Kevin)
dc.date.accessioned 2022-09-16T02:08:15Z
dc.date.available 2022-09-16T02:08:15Z
dc.date.issued 2022 en
dc.identifier.uri https://hdl.handle.net/2292/61267
dc.description.abstract In forensic casework, DNA evidence profiles are generated by amplifying short tandemly repeated lengths of DNA (STRs) using a polymerase chain reaction (PCR). DNA profiles can be challenging to interpret when they are low-level, and there is the presence of more than one individual in the DNA profile. DNA mixture interpretation can be subjective. However, forensic scientists have developed methodologies to facilitate a more objective and consistent approach to complex DNA profile interpretation over the past three decades. These are known as probabilistic genotyping methods and many of them have been coded into software. Recently, laboratories have considered adopting next-generation sequencing technologies (NGS), also known as massively parallel sequencing (MPS), for forensic DNA profiling. Sequenced-based information can increase the discriminatory power of STRs and have been advertised as improving the resolution of profiles containing more than individual (called mixtures). Few sophisticated probabilistic genotyping solutions are currently available for the interpretation of NGS DNA profiles. We explore, in this thesis, the current state of probabilistic genotyping for the interpretation of forensic STR DNA profiles generated using capillary electrophoresis (CE) instruments (Chapter 2). In Chapter 3, we describe how NGS DNA profiles are generated. Using our understanding of continuous models for CE DNA profiles and how NGS DNA profiles are generated, we develop models to calculate expected allelic and stutter signals in NGS DNA profiles. The models developed are implemented within a probabilistic genotyping software, and we test the performance of these models on the interpretation of mixtures in Chapter 4. This body of work demonstrates that we can interpret DNA mixtures generated using a sequencing technique. However, even though this solution is available, laboratories must consider several other factors before implementing the technology in their workflow and reporting the results.
dc.publisher ResearchSpace@Auckland en
dc.relation.ispartof PhD Thesis - University of Auckland en
dc.relation.isreferencedby UoA en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.rights.uri http://creativecommons.org/licenses/by-nc-sa/3.0/nz/
dc.title The Application of Modern Statistical Methods to the Advance of Probabilistic Genotyping
dc.type Thesis en
thesis.degree.discipline Statistics
thesis.degree.grantor The University of Auckland en
thesis.degree.level Doctoral en
thesis.degree.name PhD en
dc.date.updated 2022-08-16T01:59:06Z
dc.rights.holder Copyright: The author en
dc.rights.accessrights http://purl.org/eprint/accessRights/OpenAccess en


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