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下一代测序和新兴技术。

Next-Generation Sequencing and Emerging Technologies.

机构信息

Translational Genomics Group, Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.

Department of Neurogenetics, Kolling Institute, University of Sydney and Royal North Shore Hospital, St Leonards, New South Wales, Australia.

出版信息

Semin Thromb Hemost. 2024 Oct;50(7):1026-1038. doi: 10.1055/s-0044-1786397. Epub 2024 May 1.

Abstract

Genetic sequencing technologies are evolving at a rapid pace with major implications for research and clinical practice. In this review, the authors provide an updated overview of next-generation sequencing (NGS) and emerging methodologies. NGS has tremendously improved sequencing output while being more time and cost-efficient in comparison to Sanger sequencing. The authors describe short-read sequencing approaches, such as sequencing by synthesis, ion semiconductor sequencing, and nanoball sequencing. Third-generation long-read sequencing now promises to overcome many of the limitations of short-read sequencing, such as the ability to reliably resolve repeat sequences and large genomic rearrangements. By combining complementary methods with massively parallel DNA sequencing, a greater insight into the biological context of disease mechanisms is now possible. Emerging methodologies, such as advances in nanopore technology, in situ nucleic acid sequencing, and microscopy-based sequencing, will continue the rapid evolution of this area. These new technologies hold many potential applications for hematological disorders, with the promise of precision and personalized medical care in the future.

摘要

遗传测序技术发展迅速,对研究和临床实践具有重大影响。在这篇综述中,作者提供了下一代测序(NGS)和新兴方法的最新概述。与 Sanger 测序相比,NGS 极大地提高了测序输出,同时更节省时间和成本。作者描述了短读测序方法,如合成测序、离子半导体测序和纳米球测序。第三代长读测序现在有望克服短读测序的许多限制,例如能够可靠地解决重复序列和大型基因组重排问题。通过将互补方法与大规模平行 DNA 测序相结合,现在可以更深入地了解疾病机制的生物学背景。新兴方法,如纳米孔技术、原位核酸测序和基于显微镜的测序的进步,将继续推动这一领域的快速发展。这些新技术在血液病中有许多潜在的应用,有望在未来实现精准和个性化医疗。

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