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SMRT® Sequencing Solutions for Large Genomes and Transcriptomes

机译:适用于大型基因组和转录组的SMRT®测序解决方案

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摘要

Single Molecule, Real-Time (SMRT) Sequencing holds promise for addressing new frontiers in large genome complexities, such as long, highly repetitive, low-complexity regions and duplication events, and differentiating between transcript isoforms that are difficult to resolve with short-read technologies. We present solutions available for both reference genome improvement (100 MB) and transcriptome research to best leverage long reads that have exceeded 20 Kb in length. Benefits for these applications are further realized with consistent use of size-selection of input sample using the BluePippin™ device from Sage Science. Highlights from our genome improvement projects using the latest P5-C3 chemistry on model organisms with contig N50 exceeding 6 Mb and longest contig exceeding 12.5 Mb with an average base quality of QV50 will be shared. Additionally, the value of long, intact reads to provide a no-assembly approach to investigate transcript isoforms using our Iso-Seq protocol will be presented.
机译:单分子实时(SMRT)测序有望解决大型基因组复杂性方面的新领域,例如长,高度重复,低复杂性区域和重复事件,以及区分难以通过短读法解析的转录本同工型。技术。我们提供了可用于参考基因组改进(100 MB)和转录组研究的解决方案,以最佳利用长度超过20 Kb的长读段。通过使用Sage Science的BluePippin™设备始终如一地选择输入样本的大小,可以进一步实现这些应用的优势。我们将分享使用最新P5-C3化学方法对重叠群N50超过6 Mb和最长重叠群超过12.5 Mb,平均基本质量QV50的模型生物进行基因组改良项目的重点。此外,还将介绍长时间完整阅读的价值,以提供使用我们的Iso-Seq协议研究转录异构体的无装配方法。

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