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An integrative analysis of ctDNA fragmentomics and methylation across breast cancer subtypes to identify subtype-specific prognostic biomarkers

bracu.type.groupStudent Works
dc.contributor.advisorShishir, Tushar Ahmed
dc.contributor.authorRaida, Ruhin Rahman
dc.contributor.authorKaniz, Nafisa
dc.contributor.authorFerdaus, Tarunima
dc.contributor.departmentDepartment of Mathematics and Natural Sciences
dc.date.accessioned2026-02-22T05:51:58Z
dc.date.available2026-02-22T05:51:58Z
dc.date.copyright2025
dc.date.copyright2025
dc.date.issued2025-12
dc.descriptionThis thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Science in Biotechnology, 2025.en_US
dc.descriptionCatalogued from PDF version of thesis.
dc.descriptionIncludes bibliographical references (pages 63-69).
dc.description.abstractIn cancer patients, a substantial fraction of cell-free DNA (cfDNA), derived from tumor cells, offers a non-invasive opportunity to interrogate tumor biology. This study aimed to extract, profile and identify unique fragmentation and methylation patterns in four different breast cancer subtypes (HER2+, Luminal B, Triple Negative Breast Cancer, Triple Positive Breast Cancer) compared to healthy controls. Furthermore, it utilizes the fragmentation feature profiles along with epigenetic analysis to evaluate their potential for subtype -specific detection. Public cfDNA sequencing datasets from healthy controls and four types of breast cancer subtypes cases were retrieved from the NCBI SRA repository. Fragmentation features including Fragment Size Distribution (FSD), Fragmentation Size Ratio (FSR), Fragmentation Size Coverage (FSC), BreakPoint Motif (BPM), End Motif (EDM), Copy Number Variation (CNV) and epigenetics profiles like methylation profiles were searched using a python based workflow and downstream analyzed in R. Our findings indicated subtype specific distinctions in TNBC and TPBC, where notable differences in fragmentation and methylation patterns were observed when compared with controls and other subtypes. Among the fragmentomic features evaluated, Fragment Size Ratio showed noticeable difference for TPBC and TNBC but did not demonstrate the same level of distinction for LB or HER2+. In methylation, end motif and breakpoint motif analyses, observable patterns were also more prominent in TNBC and TPBC, while clear differentiation was not consistently evident for LB and HER2+ within this dataset. The integrated analysis of cfDNA hypermethylation and fragmentomic features reveal distinct fragmentation signatures in TPBC and TNBC, emphasizing the potential of cfDNA-based assays for precise, non-invasive molecular subtyping and the development of liquid biopsy strategies for early detection and disease monitoring.en_US
dc.description.degreeBachelor of Science in Biotechnology
dc.description.statementofresponsibilityRuhin Rahman Raida
dc.description.statementofresponsibilityNafisa Kaniz
dc.description.statementofresponsibilityTarunima Ferdaus
dc.format.extent73 pages
dc.identifier.otherID 21336025
dc.identifier.otherID 21336012
dc.identifier.otherID 21236063
dc.identifier.urihttp://hdl.handle.net/10361/27539
dc.language.isoenen_US
dc.publisherBRAC Universityen_US
dc.rightsBRAC University theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission.
dc.subjectcfDNAen_US
dc.subjectFragmentomicsen_US
dc.subjectMethylationen_US
dc.subjectBreast canceren_US
dc.subjectMolecular subtypesen_US
dc.subject.lcshBreast--Cancer.
dc.subject.lcshDNA--Methylation.
dc.subject.lcshBiological markers.
dc.subject.lcshMolecular microbiology.
dc.titleAn integrative analysis of ctDNA fragmentomics and methylation across breast cancer subtypes to identify subtype-specific prognostic biomarkersen_US
dc.typeThesisen_US

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