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Motivation Next generation sequencing technologies have been decreasing the costs and increasing the world-wide capacity for sequence production at an unprecedented rate, making the initiation of large scale projects aiming to sequence almost 2000 genomes [1]. Structural variation detection promises to be one of the key diagnostic tools for cancer and other diseases with genomic origin. In this paper,...
Recent studies show that, along with single nucleotide polymorphisms and small indels, larger structural variants among human individuals are common. These studies have typically been based high-cost library generation and Sanger sequencing; however, recent introduction of next-generation sequencing (NGS) technologies is changing how research in this area is conducted in a significant way. Highthroughput...
Evolving technological sophistication has resulted in ongoing modifications of traditional surgical approaches to correct disorders of the spinal axis. Advances in instrumentation and pre- and intraoperative imaging have fueled a move toward minimally invasive, minimal access spine surgery (1), by which the same surgical goals of conventional open techniques are met through a smaller access corridor...
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