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Massachusetts Institute of Technology

Automated, highly scalable RNA-seq analysis

Abstract

dc:description.abstract

RNA-sequencing is a sensitive method for inferring gene expression and provides additional information regarding splice variants, polymorphisms and novel genes and isoforms. Using this extra information greatly increases the complexity of an analysis and prevents novice investigators from analyzing their own data. The first chapter of this work introduces a solution to this issue. It describes a community-curated, scalable RNA-seq analysis framework for performing differential transcriptome expression, transcriptome assembly, variant and RNA-editing calling. It handles the entire stack of an analysis, from downloading and installing hundreds of tools, libraries and genomes to running an analysis that is able to be scaled to handle thousands of samples simultaneously. It can be run on a local machine, any high performance cluster or on the cloud and new tools can be plugged in at will. The second chapter of this work uses this software to examine transcriptome changes in the cortex of a mouse model of tuberous sclerosis with a neuron-specific knockout of Tsc1. We show that upregulation of the serotonin receptor Htr2c causes aberrant calcium spiking in the Tsc1 knockout mouse, and implicate it as a novel therapeutic target for tuberous sclerosis. The third chapter of this work investigates transcriptome regulation in the superior colliculus with prolonged eye closure. We show that while the colliculus undergoes long term anatomical changes with light deprivation, the gene expression in the colliculus is unchanged, barring a module of genes involved in energy production. We use the gene expression data to resolve a long-standing debate regarding the expression of dopamine receptors in the superior colliculus and found a striking segregation of the Drd1 and Drd2 dopamine receptors into distinct functional zones.

Degree

thesis:*
Department dc:contributor.department
Harvard--MIT Program in Health Sciences and Technology.
Grantor dc:publisher
Massachusetts Institute of Technology
Year dc:date.issued
2015

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Kirchner, Rory
Advisor dc:contributor.advisor
  • Martha Constantine-Paton.

Subjects

dc:subject × 1

Rights

dc:rights
Statement dc:rights
  • M.I.T. 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. See provided URL for inquiries about permission.
Language dc:language.iso
eng

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/1721.1/101340
OAI identifier oai:identifier
oai:dspace.mit.edu:1721.1/101340

Chain of custody

source
Harvested from
MIT
Base URL
dspace.mit.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Kirchner, Rory. Automated, highly scalable RNA-seq analysis. Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/101340