The bottleneck in developing clinical applications of next generation sequencing is the storage and analysis of the large volumes of data that are generated the applications are diverse but the common themes are computational and analytically challenging. Clinical applications for next generation sequencing provides readers with an outstanding postgraduate resource to learn about the translational use of ngs in clinical environments rooted in both medical genetics and clinical medicine the book fills the gap between state of the art technology and evidence based practice providing an educational opportunity for users to advance patient . This article will review recent impact of massively parallel next generation sequencing ngs in our understanding and treatment of cancer while whole exome sequencing wes remains popular and effective as a method of genetically profiling different cancers advances in sequencing technology has enabled an increasing number of whole genome based studies. Next generation sequencing has fundamentally impacted biomedical research and is poised to begin a transition into the clinical diagnostic space ngs is still relatively early its evolution it is fast paced and new developments are expected for the foreseeable future. In the case of a negative genetic test for a patient with a clear clinical phenotype experts encourage establishing cooperation with a scientific laboratory looking out for novel disease causing variants but it is also possible to consider commercially available clinical exome or genome sequencing an important aspect of next generation
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