Genomic analysis is the identification, measurment, and/or comparison of genomic features (like DNA sequences) on a genomic (i.e., the study of all of a person's genes) scale. 
            
            
            
         
     
    
        
                    
                                    
                
         
                
                    
                                        
                                    
                                                                    
                                    
                                    
                                                                    
                                    
                                        
    
    
    
        Patients with chromosomal rearrangements resulting in fusion proteins are among the most responsive to published targeted therapy. For example, targeting of the EML4-ALK fusion in non-small c...
    
    
            
     
                                     
                                    
                                                                    
                                    
                                        
    
            
    
    
    
        Late-stage drug attrition rates in oncology remain higher than in other therapeutic areas. To reduce attrition, it is critical to identify appropriate drug targets and pre-clinical models. Th...
    
    
            
     
                                     
                                    
                                                                    
                                    
                                    
                                                                    
                                    
                                        
    
    
    
        Rare disorder analysis has been facilitated by the declining cost of sequencing. Despite numerous success stories the underlying cause remains unexplained in >50% cases, emphasizing the ne...
    
    
            
     
                                     
                                    
                                                                    
                                    
                                        
    
            
    
    
    
        The comprehensive, multidimensional molecular characterization of tumors and the individuals in which they have developed is transforming cancer definition, diagnosis, treatment, and preventi...
    
    
            
     
                                     
                                    
                                                                    
                                    
                                        
    
    
    
        In this presentation I describe pathway based analyses of genotyping data to identify pathways related to the development of complex diseases, with a focus on lung cancer and selected autoimm...
    
    
            
     
                                     
                                    
                                                                    
                                    
                                        
    
            
    
    
    
        Next-Generation Sequencing is enabling scientists to study the transcriptome in ways never before possible.  During this session with Illumina Distinguished Scientist, Dr. Gary Schroth, you w...
    
    
            
     
                                     
                                    
                                                                    
                                    
                                        
    
            
    
    
    
        Whole genomic and exomics sequencing applied clinically is revealing newly discovered genes and syndromes at an astonishing rate. While clinical databases and variant annotation continue to g...
    
    
            
     
                                     
                                    
                                                                    
                                    
                                        
    
            
    
    
    
        Understanding how genes coordinate their expression across cells in a growing embryo can provide insights into the transcriptional programs that control development. Intercellular variability...
    
    
            
     
                                     
                                    
                                                                    
                                    
                                        
    
            
    
    
    
        Genome and exome sequencing are widely used for both basic and clinical research and diagnosis. Although sequencing costs have dropped dramatically and technology and algorithms used for call...
    
    
            
     
                                     
                                    
                                                                    
                                    
                                        
    
            
    
    
    
        The flexibility of the BioMark Real-Time PCR System, allow us to preform genetic research using different types of nano-fluidic (48.48 or 96.96) chips setup, in the thermal cycle of these chi...
    
    
            
     
                                     
                                    
                                                                    
                                    
                                        
    
            
    
    
    
        Next-generation sequencing (NGS) has revolutionized extraction of genomic information, facilitating rapid advances in the fields of clinical research and molecular diagnostics. However, c...
    
    
            
     
                                     
                                    
                                                                    
                                    
                                        
    
    
    
        Structural variants (SVs), defined as the deletion, duplication, insertion, inversion or translocation of genomic regions, are both a major source of genetic diversity in human populations an...