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Single-cell next Generation Sequencing and Its Applications in Cancer Biology.- Utility of Next Generation Sequencing in Cancer Drug Development and Clinical Trials.- Next-Generation Sequencing in the Era of Cancer-Targeted Therapies: Towards the Personalised Medicine.- Mutational Similarities Across Cancers: Implications for Research, Diagnostics and Personalized Therapy Design.- Standardized Decision Support in NGS Reports of Somatic Cancer Variants.- Clinical Considerations in the Conduct of Cancer Next Generation Sequencing Testing and Genetic Counselling.- Next Generation Sequencing for Cancer Biomarker Discovery.- Validation and Implementation of Next Generation Sequencing Technologies in a Clinical Molecular Diagnostic Laboratory.- Next Generation Sequencing Technologies and Formalin Fixed Paraffin Embedded Tissue: Application to Clinical Cancer Research.- Applications of NGS to Screen FFPE Tumours for Detecting Fusion Transcripts.- Clinical Application of Next-Generation Sequencing of Formalin-Fixed Paraffin-Embedded Tumors.- ChIP-BS-Sequencing in Cancer Epigenomics.- Integrative Analysis Identifies Transcription Factor-DNA Methylation Relationships and Introduces New Avenues for Translating Cancer Epigenetics Into the Clinic.- Differential Methylation Analysis with Next-Generation Sequencing.- Performance Comparison and Data Analysis Strategies for MicroRNA Profiling in Cancer Research.- Small RNA Sequencing for Squamous Cell Carcinoma Research.- Exome Capture and Capturing Technologies in Cancer Research.- The Landscape of DNA Virus Associations Across Human Malignant Cancers.- Using Next Generation Sequencing to Reveal Patterns of Chromosomal Alterations in Oral Verrucous Carcinoma.- Vironomics: The Study of Viral Genomics in Human Cancer and Disease.- Molecular Typing of Lung Adenocarcinoma on Cytological Samples in the Next Generation Sequencing Era.- Whole Genome/Exome Sequencing in Acute Leukemia: From Research to Clinics.- Next Generation Sequencing Applications in Head and Neck Oncology.- CIC Mutation in Brain Tumor.- Isocitrate Dehydrogenase (IDH) Mutation in Gliomas.- Utilization of Multigene Panels in Hereditary Cancer Predisposition Testing.
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