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Dissertation/Thesis Abstract

Classification of Breast Cancer Patients and NCI-60 Cell Lines Using a Novel SNV-based Phylogenetic Analysis Method
by Faison, William J., M.S., The George Washington University, 2014, 48; 1556736
Abstract (Summary)

Next-generation sequencing data can be mapped to a reference genome to identify singlenucleotide polymorphisms/variations (SNPs/SNVs; called SNPs hereafter). In theory, SNPs can be compared across several samples and the differences can be used to create phylogenetic trees depicting relatedness among the samples. However, in practice this is difficult because currently there is no stand-alone tool that takes SNP data directly as input and produces phylogenetic trees. In response to this need, PhyloSNP application was created with two analysis methods: 1) a quantitative method that creates the presence/absence matrix which can be directly used to generate phylogenetic trees or creates a tree from a shrunk genome alignment (includes additional bases surrounding the SNP position), and 2) a qualitative method that clusters samples based on the frequency of different bases found at a particular position. The algorithms were used to generate trees from Poliovirus, Burkholderia and human cancer genomics NGS datasets.

The NCI-60 cell line has been extensively researched [1-3]. These lines were aligned and profiled from lllumina exome data using the High-performance Integrated Virtual Environment (HIVE) and phylogenetic trees were generated using PhyloSNP and FastTree based on the discovered SNPs. These trees were used to determine whether there were any noticeable relationships between the cancer lines. We noticed that several melanoma cell lines (ME:MDA_MB_435, ME:MDA_N, ME:UACC_62, and ME:M14) and breast (BR:HS578T, BR:T47D, and BR:MCF7) grouped together in both total variation and non-dbSNP variation trees with near 100% bootstrap support (10,000 replicates). Preliminary findings show that the observed phylogenetic clustering of these seven cell lines is at least partially due to some altered motif and common involvement of the TP53 gene to each of these cancer types. However, more in depth analysis is required to elucidate on these potential findings.

Indexing (document details)
Advisor: Mazumder, Raja
Commitee: Nair, Sujit
School: The George Washington University
Department: School of Medicine and Health Sciences
School Location: United States -- District of Columbia
Source: MAI 53/01M(E), Masters Abstracts International
Subjects: Bioinformatics, Oncology
Keywords: Breast cancer, Cancer genomics, Next-generation sequencing, Phylogenetic, SNP, SNV
Publication Number: 1556736
ISBN: 978-1-303-92725-6
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