Title Page
ABSTRACT
Contents
1. INTRODUCTION 9
2. MATERIALS AND METHODS 13
2.1. Data Source 13
2.2. Hi-C Sequencing Library Preparation 13
2.3. Hi-C Data Processing 14
2.4. Structural Variants Detection 15
2.5. Haplotype Phasing 15
3. RESULTS 16
3.1. Hi-C data set of tissue samples from HNSCC patients 16
3.2. Translocation Identification in HNSCC Hi-C data 16
3.3. Cross-validation with SVs detected in WGS 17
3.4. Haplotype-resolved SVs identification 17
4. DISCUSSION 25
5. REFERENCES 27
국문 초록 30
Figure 1. Hi-C data set of tissue samples from HNSCC patients 20
Figure 2. Cross-validation with SVs detected in WGS 21
Figure 3. Translocation Identification in HNSCC Hi-C data 22
Figure 4. Haplotype-resolved SVs identification 23