Identification of insertion-induced enhancers linked to gene drivers within non-coding DNA using a pipeline for diffuse large b-cell lymphoma H3K27ac ChIP-seq data

dc.contributor.advisorBendou, Hocine
dc.contributor.authorJassiem, Wardah
dc.date.accessioned2023-05-18T08:12:44Z
dc.date.accessioned2024-05-17T07:20:05Z
dc.date.available2023-05-18T08:12:44Z
dc.date.available2024-05-17T07:20:05Z
dc.date.issued2022
dc.descriptionMasters of Scienceen_US
dc.description.abstractDiffuse large B-cell lymphoma (DLBCL) is the most common subtype of non-Hodgkin lymphoma (NHL) and incorporates a diverse range of illnesses with varying biology, clinical manifestations, and therapeutic responses. Functional insertion mutations represent the driving mechanism behind many oncologic illnesses. Research has shown that variants associated with cancer in the non-coding portion of the genome, which is enriched with enhancer elements, is greatly underappreciated. The present study designed a bioinformatics pipeline using Nextflow DSL2 to identify insertion-induced enhancers associated with DLBCL oncogenes within the non-coding genome using H3K27ac ChIP-seq data. Gapped DLBCL reads identified by bowtie were mapped to the human reference genome with bowtie2. Non-coding insertions were identified with BEDTools and verified by pBla.en_US
dc.identifier.urihttps://hdl.handle.net/10566/15224
dc.language.isoenen_US
dc.publisherUniversity of the Western Capeen_US
dc.rights.holderUniversity of the Western Capeen_US
dc.subjectCanceren_US
dc.subjectDiffuse large B-cell lymphomaen_US
dc.subjectEnhanceren_US
dc.subjectInsertionen_US
dc.subjectPipelineen_US
dc.titleIdentification of insertion-induced enhancers linked to gene drivers within non-coding DNA using a pipeline for diffuse large b-cell lymphoma H3K27ac ChIP-seq dataen_US

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