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首页> 外文期刊>Journal of Biotechnology >The Genome Sequencer FLX(TM) System-Longer reads, more applications, straight forward bioinformatics and more complete data sets
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The Genome Sequencer FLX(TM) System-Longer reads, more applications, straight forward bioinformatics and more complete data sets

机译:Genome Sequencer FLX(TM)系统读者阅读,更多应用,直接的生物信息学和更完整的数据集

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摘要

The Genome Sequencer FLX System (GS FLX), powered by 454 Sequencing, is a next-generation DNA sequencing technology featuring a unique mix of long reads, exceptional accuracy, and ultra-high throughput. It has been proven to be the most versatile of all currently available next-generation sequencing technologies, supporting many high-profile studies in over seven applications categories. GS FLX users have pursued innovative research in de novo sequencing, re-sequencing of whole genomes and target DNA regions, metagenomics, and RNA analysis. 454 Sequencing is a powerful tool for human genetics research, having recently re-sequenced the genome of an individual human, currently re-sequencing the complete human exome and targeted genomic regions using the NimbleGen sequence capture process, and detected low-frequency somatic mutations linked to cancer.
机译:由454测序技术提供支持的Genome测序仪FLX系统(GS FLX)是下一代DNA测序技术,具有长读取,卓越的准确性和超高通量的独特组合。它被证明是当前所有可用的下一代测序技术中功能最丰富的,可支持超过七个应用类别中的许多引人注目的研究。 GS FLX用户在从头测序,整个基因组和目标DNA区域的重测序,宏基因组学和RNA分析方面进行了创新的研究。 454测序是人类遗传学研究的强大工具,最近对单个人类的基因组进行了重新测序,目前使用NimbleGen序列捕获过程对完整的人类外显子组和目标基因组区域进行了重新测序,并检测到了低频体细胞突变致癌。

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