Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.746540
Title: Improving the prediction of transcription factor binding sites to aid the interpretation of non-coding single nucleotide variants
Author: Jayaram, N.
ISNI:       0000 0004 7224 4688
Awarding Body: UCL (University College London)
Current Institution: University College London (University of London)
Date of Award: 2017
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Please try the link below.
Access from Institution:
Abstract:
Single nucleotide variants (SNVs) that occur in transcription factor binding sites (TFBSs) can disrupt the binding of transcription factors and alter gene expression which can cause inherited diseases and act as driver SNVs in cancer. The identification of SNVs in TFBSs has historically been challenging given the limited number of experimentally characterised TFBSs. The recent ENCODE project has resulted in the availability of ChIP-Seq data that provides genome wide sets of regions bound by transcription factors. These data have the potential to improve the identification of SNVs in TFBSs. However, as the ChIP-Seq data identify a broader range of DNA in which a transcription factor binds, computational prediction is required to identify the precise TFBS. Prediction of TFBSs involves scanning a DNA sequence with a Position Weight Matrix (PWM) using a pattern matching tool. This thesis focusses on the prediction of TFBSs by: (a) evaluating a set of locally-installable pattern-matching tools and identifying the best performing tool (FIMO), (b) using the ENCODE ChIP-Seq data to evaluate a set of de novo motif discovery tools that are used to derive PWMs which can handle large volumes of data, (c) identifying the best performing tool (rGADEM), (d) using rGADEM to generate a set of PWMs from the ENCODE ChIP-Seq data and (e) by finally checking that the selection of the best pattern matching tool is not unduly influenced by the choice of PWMs. These analyses were exploited to obtain a set of predicted TFBSs from the ENCODE ChIP-Seq data. The predicted TFBSs were utilised to analyse somatic cancer driver, and passenger SNVs that occur in TFBSs. Clear signals in conservation and therefore Shannon entropy values were identified, and subsequently exploited to identify a threshold that can be used to prioritize somatic cancer driver SNVs for experimental validation.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.746540  DOI: Not available
Share: