Convergence of regulatory mutations into oncogenic pathways across multiple tumor types

Thesis: S.M., Massachusetts Institute of Technology, Computation for Design and Optimization Program, 2017. === Cataloged from PDF version of thesis. === Includes bibliographical references (pages 65-74). === Cancer sequencing efforts have largely focused on profiling somatic variants in the protein...

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Bibliographic Details
Main Author: Murugadoss, Karthik
Other Authors: Manolis Kellis.
Format: Others
Language:English
Published: Massachusetts Institute of Technology 2017
Subjects:
Online Access:http://hdl.handle.net/1721.1/111510
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spelling ndltd-MIT-oai-dspace.mit.edu-1721.1-1115102019-05-02T16:25:25Z Convergence of regulatory mutations into oncogenic pathways across multiple tumor types Murugadoss, Karthik Manolis Kellis. Massachusetts Institute of Technology. Computation for Design and Optimization Program. Massachusetts Institute of Technology. Computation for Design and Optimization Program. Computation for Design and Optimization Program. Thesis: S.M., Massachusetts Institute of Technology, Computation for Design and Optimization Program, 2017. Cataloged from PDF version of thesis. Includes bibliographical references (pages 65-74). Cancer sequencing efforts have largely focused on profiling somatic variants in the protein-coding genome and characterizing their functional impact. In this study, we develop a computational pipeline to identify non-coding mutational drivers across multiple tumor types. We describe the non-coding mutational profiles of 854 samples, spread across 15 tumor types, in the context of their respective tissue type-specific reference epigenomes, using recent pan-cancer whole-genome sequencing data. We develop a novel method to detect significantly recurrent non-coding mutations by reestimating the background mutation density while adjusting for epigenomic covariates. Existing databases on enhancer-gene links allow us to capture the convergence of disparate mutations onto downstream target genes. We then systematically identify key immunomodulatory and tumor-suppressive genes enriched for non-coding mutations in their regulatory neighborhood and evaluate these in a pan-cancer context. Taken together, we show that low-frequency alterations converge into high-frequency recurrent events on downstream targets through tissue-specific regulatory interactions. by Karthik Murugadoss. S.M. 2017-09-15T15:37:21Z 2017-09-15T15:37:21Z 2017 2017 Thesis http://hdl.handle.net/1721.1/111510 1003324173 eng MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission. http://dspace.mit.edu/handle/1721.1/7582 74 pages application/pdf Massachusetts Institute of Technology
collection NDLTD
language English
format Others
sources NDLTD
topic Computation for Design and Optimization Program.
spellingShingle Computation for Design and Optimization Program.
Murugadoss, Karthik
Convergence of regulatory mutations into oncogenic pathways across multiple tumor types
description Thesis: S.M., Massachusetts Institute of Technology, Computation for Design and Optimization Program, 2017. === Cataloged from PDF version of thesis. === Includes bibliographical references (pages 65-74). === Cancer sequencing efforts have largely focused on profiling somatic variants in the protein-coding genome and characterizing their functional impact. In this study, we develop a computational pipeline to identify non-coding mutational drivers across multiple tumor types. We describe the non-coding mutational profiles of 854 samples, spread across 15 tumor types, in the context of their respective tissue type-specific reference epigenomes, using recent pan-cancer whole-genome sequencing data. We develop a novel method to detect significantly recurrent non-coding mutations by reestimating the background mutation density while adjusting for epigenomic covariates. Existing databases on enhancer-gene links allow us to capture the convergence of disparate mutations onto downstream target genes. We then systematically identify key immunomodulatory and tumor-suppressive genes enriched for non-coding mutations in their regulatory neighborhood and evaluate these in a pan-cancer context. Taken together, we show that low-frequency alterations converge into high-frequency recurrent events on downstream targets through tissue-specific regulatory interactions. === by Karthik Murugadoss. === S.M.
author2 Manolis Kellis.
author_facet Manolis Kellis.
Murugadoss, Karthik
author Murugadoss, Karthik
author_sort Murugadoss, Karthik
title Convergence of regulatory mutations into oncogenic pathways across multiple tumor types
title_short Convergence of regulatory mutations into oncogenic pathways across multiple tumor types
title_full Convergence of regulatory mutations into oncogenic pathways across multiple tumor types
title_fullStr Convergence of regulatory mutations into oncogenic pathways across multiple tumor types
title_full_unstemmed Convergence of regulatory mutations into oncogenic pathways across multiple tumor types
title_sort convergence of regulatory mutations into oncogenic pathways across multiple tumor types
publisher Massachusetts Institute of Technology
publishDate 2017
url http://hdl.handle.net/1721.1/111510
work_keys_str_mv AT murugadosskarthik convergenceofregulatorymutationsintooncogenicpathwaysacrossmultipletumortypes
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