Sökning: "Predictive Coding"
Visar resultat 11 - 15 av 23 avhandlingar innehållade orden Predictive Coding.
11. MicroRNAs in HER2-Amplified Breast Cancer
Sammanfattning : Background: Breast cancer is the most common female malignancy and the leading cause of cancer-related deaths worldwide. Targeted therapy against the main biomarkers estrogen receptor alpha (ER) and human epidermal growth factor receptor 2 (HER2/ERBB2) have greatly improved mortality rates, but ab initio or acquired therapy resistance is common. LÄS MER
12. Prognostic Markers in Diffuse Large B-cell Lymphoma : How Bad can it be
Sammanfattning : Diffuse large B-cell lymphoma (DLBCL), which is the most common type of lymphoma, is characterised by its aggressiveness and poor outcome without adequate treatment and also for its biological and clinical heterogeneity. It is therefore highly desirable to gain a more profound understanding of the underlying biology of the disease, as well as predictive factors for the guidance of treatment. LÄS MER
13. Diverticular disease of the colon - risk factors and validation of diagnosis
Sammanfattning : Diverticular Disease (DD) is a common gastrointestinal disease, particularly among the population in western countries. The aetiology of DD is complex and have not yet been established conclusively. Dietary habits and lifestyle choices such as, physical inactivity, obesity, and smoking, affects the development of the disease. LÄS MER
14. Interframe Quantization for Noisy Channels
Sammanfattning : The demand for efficient transmission and storage of, for example, speech signals poses high requirements on the development of signal compression techniques. This thesis deals with vector quantization (VQ) which is a powerful technique for signal compression. LÄS MER
15. Exploring next-generation sequencing in chronic lymphocytic leukemia
Sammanfattning : Next-generation sequencing (NGS) techniques have led to major breakthroughs in the characterization of the chronic lymphocytic leukemia (CLL) genome with discovery of recurrent mutations of potential prognostic and/or predictive relevance. However, before NGS can be introduced into clinical practice, the precision of the techniques needs to be studied in better detail. LÄS MER