Chapter 2 - University of British Columbia

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2.3.6 Analysis of data from a single assay type The first, and most basic, level of analysis is from a single assay type. For array CGH, multiple options for segmentation algorithms are available within the program and results from externally run segmentation can be imported as well. However, each segmentation algorithm has its advantages and disadvantages depending on the type of data used and the quality of data at hand. A unique feature of SIGMA 2 is the ability to take a consensus of multiple algorithms using "And" or "Or" logic between algorithms. Moreover, a level of consensus can be specified (Figure 2.5a). For example, if an experiment is analyzed using five approaches, the user can select areas of gain and loss which were detected by one algorithm, at least three algorithms, all five algorithms, etc. For LOH, basic analysis using the number of consecutive markers that exhibit LOH is used to determine its status. Affinity-based approaches for DNA methylation and histone modification states or bead-based percentage of CpG island methylation is analyzed by either direct thresholding or z-transform thresholding. For any of the different assay types, when examining across a number of samples, a frequency of alteration can be calculated and plotted. For data from different array platforms, but assaying the same biological measurement, the algorithm for integration is used to derive common data. This feature is most applicable to DNA copy number data due to the number of array CGH platforms. This allows for better utilization of publicly available data and thus, increasing sample size for statistical analysis. Similar to the multiple sample analysis of data on the sample platform, a frequency of altered states can be generated and plotted. Figure 5A shows the concerted analysis of a sample profiled on the Affymetrix 500K SNP array, Agilent 244K CGH array and the whole genome tiling path BAC array (Figure 2.5b). 29
2.3.7 Analysis of data from multiple assays in a given 'omics dimension Within a given 'omics dimension, multiple assay types can be analyzed in combination. For example, it is useful to investigate copy number and LOH and the interplay between DNA methylation and different states of histone modification. Typically, in regions of copy number loss, LOH is also observed. However, LOH can also occur in regions which are copy number neutral, indicating a change in allelic status which is not interpretable by one dimension alone. Here, we show a sample for which copy number and LOH information exists, a region of copy number loss associated with LOH (Figure 2.6). In terms of epigenetics, DNA methylation and states of histone methylation and acetylation have been known to be biologically relevant. With high throughput technologies available to assay these dimensions, this type of analysis will become more prevalent. 2.3.8 Combinatorial analysis of multiple 'omics dimensions - gene dosage and gene expression The most common analysis of multiple 'omics dimensions is the influence of the genome on the transcriptome. A number of software packages have started to incorporate approaches to examining gene dosage and gene expression [8, 9, 27]. In SIGMA 2 , there are multiple functionalities which allow the user to link DNA copy number to gene expression. For a single group of samples, with matching DNA copy number and gene expression profiles, the user can determine associations through two main options: a) using a correlation-based approach, correlating the log ratios with the normalized gene expression intensities and b) using a statistical-based approach comparing the expression in samples with copy number changes against those without copy number change utilizing the Mann Whitney U test, analogous to approaches taken in previous studies [27]. Spearman, Kendall or Pearson correlation coefficients can be calculated for option a). Similarly, this functionality is also available for correlating epigenetic profiles and gene expression. 30
Page 1 and 2: DEVELOPMENT AND APPLICATION OF AN I
Page 3 and 4: Table of Contents Abstract ........
Page 5 and 6: 3.3.2 Multi-dimensional analysis (M
Page 7 and 8: List of Tables Table 2.1. Features
Page 9 and 10: Figure 5.3. Overlay of chromosomal
Page 11 and 12: RB1 Retinoblastoma 1 RNA Ribonuclei
Page 13 and 14: Dedication To my family. xiii
Page 15 and 16: Chapter 5: Chari R, Thu KL, Wilson
Page 17 and 18: 1.1 Lung cancer Lung cancer has the
Page 19 and 20: expression changes are reactive to
Page 21 and 22: number of different cancer types. M
Page 23 and 24: large number of tumors, that a give
Page 25 and 26: (B) By using an integrative approac
Page 27 and 28: platforms, with one of the latest s
Page 29 and 30: 1.12.1 Development of tools for gen
Page 31 and 32: quantitative PCR experiments as wel
Page 33 and 34: 1.13 References 1. Jemal A, Siegel
Page 35 and 36: 33. Garber ME, Troyanskaya OG, Schl
Page 37 and 38: 71. Shivapurkar N, Gazdar AF: DNA M
Page 39 and 40: Chapter 2: SIGMA 2 : A system for t
Page 41 and 42: Here, we present SIGMA 2 , a novel
Page 43: datasets. To utilize this, the user
Page 47 and 48: expression (Figure 2.8). ERBB2 has
Page 49 and 50: Figure 2.1 R -Segmentation -Statist
Page 51 and 52: Figure 2.3 numSamples
Page 53 and 54: Figure 2.5. Consensus calling and h
Page 55 and 56: Figure 2.6 HCC2218 HCC2218 HCC2218B
Page 57 and 58: Figure 2.8. Multi-dimensional persp
Page 59 and 60: Table 2.1. Features required for in
Page 61 and 62: 2.6 References 1. Garnis C, Buys TP
Page 63 and 64: Chapter 3: An integrative multi-dim
Page 65 and 66: observed gene expression deregulati
Page 67 and 68: Raw gene expression profiles from a
Page 69 and 70: screening approach to gene amplific
Page 71 and 72: many regions of frequent LOH/AI do
Page 73 and 74: approach to examining the whole gen
Page 75 and 76: PTEN expression [44]. Using this pa
Page 77 and 78: mechanisms at the DNA and RNA level
Page 79 and 80: In this study, three DNA dimensions
Page 81 and 82: Figure 3.2. Quantitative and qualit
Page 83 and 84: Figure 3.3 a Proportion of genes in
Page 85 and 86: 70 Figure 3.5 -log(pvalue) 5.0 4.0
Page 87 and 88: 72 Figure 3.7 Sample: HCC1008 Copy
Page 89 and 90: Figure 3.8 a b Proportion of random
Page 91 and 92: 16. Chari R, Lockwood WW, Coe BP, C
Page 93 and 94: 50. Giovane A, Pintzas A, Maira SM,
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4.1 Introduction Genetic alteration
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4.2.3 Determining frequent regions
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etween loss and UPD (Figure 4.3). S
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obtained, profiled and used as the
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Figure 4.1. Detection of UPD using
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Figure 4.2. Comparison of frequent
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Figure 4.3 Gain Loss 642 441 7 Figu
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94 Figure 4.4 1 2 3 4 5 6 7 8 9 10
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Figure 4.6 a b c Percent of cases A
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Figure 4.7 a b 6p25.3 Log2 fold cha
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Chr BPStart BPEnd # of Chr BPStart
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Table 4.3. Overlap of oncogenes in
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Table 4.5. Cell lines and oncogene
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Table 4.7. RefSeq genes in focal re
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4.6 References 1. Bell DW: Our chan
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33. Garnis C, Coe BP, Lam SL, MacAu
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5.1 Introduction In the past decade
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polymorphism (SNP) arrays with over
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substitutions) and UV exposure (C t
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developed antibodies and methylated
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Histone modification states. While
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metastasis [226]. High throughput a
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Implications on sample size require
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analyzed using the "minet" package
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expression. The next challenge is t
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Figure 5.2 # of copies Total copy n
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Figure 5.4. Integration of copy num
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Figure 5.5. Integration of copy num
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Figure 5.6 SHC1 GRB2 SOS2 RRAS ER R
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Figure 5.8 a Log2 Fold Change (T vs
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Figure 5.10 (a) (b) Figure 5.10. Au
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Table 5.2. List of genomic resource
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5.5 References 1. Pinkel D, Segrave
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37. Oliphant A, Barker DL, Stuelpna
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75. Selzer RR, Richmond TA, Pofahl
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111. Melcher R, Al-Taie O, Kudlich
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145. Takai D, Yagi Y, Wakazono K, O
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179. Kondo M, Suzuki H, Ueda R, Osa
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alterations in human prostate cance
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248. Xi L, Feber A, Gupta V, Wu M,
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281. Fernandez-Ranvier GG, Weng J,
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Chapter 6: Conclusions 162
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can identify nearly three times as
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was identified in a small set of sa
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will be done at the pathway level a
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previously described genetic and ep
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16. Zhang K, Li JB, Gao Y, Egli D,
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APPENDIX I: List of publications Th
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This publication is described in se
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This chapter details the technologi
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epigenetic alteration. This led to
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This manuscript describes the curre
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APPENDIX III: Sources of data Sampl
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APPENDIX V: Kaplan-Meier and Oncomi
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APPENDIX VI: Summary of Kaplan-Meie
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University of British Columbia - Br
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Chapter 2 - University of British Columbia

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