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Mapping the Korean Genome

机译:映射韩国基因组

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Agilent Technologies, Inc has announced that scientists using an Agilent custom-designed comparative genomic hybridisation (CGH) array have sequenced the entire gene map of a Korean male. An international team led by researchers at Seoul National University published the results in Nature. The study, 'A highly annotated whole-genome sequence of a Korean individual', published in Nature, is the second Korean genome to be sequenced in recent months and the seventh complete human genome to be published in the past two years. "Through our studies, we have discovered that a much more accurate annotation of CNVs can be obtained for a given individual's genome when you combine data from high-resolution CGH experiments with whole-genome DNA sequencing data obtained using next-generation sequencing strategies," said Dr Charles Lee, Associate Professor, Harvard Medical School and Brigham & Women's Hospital, and one of the researchers of study. "In this case, we developed and used a customised, high-resolution CNV array set, manufactured by Agilent, containing 24 million oligonucleotide probes. It would be great to see similar approaches being used for comprehensively identifying CNVs in more individuals."
机译:Agilent Technologies,Inc已宣布,使用安捷伦定制设计的比较基因组杂交(CGH)阵列的科学家对韩国男性的整个基因图进行了测序。首尔国立大学研究人员领导的国际团队发表了自然界的结果。这项研究是“韩国人的高度注释的全基因组序列”,在自然界中发表,是近几个月来测序的第二个韩国基因组,并且在过去两年中发表了第七个完整的人类基因组。 “通过我们的研究,我们发现,当您将使用下一代测序策略获得的全基因组DNA测序数据与全基因组DNA测序数据结合在一起时,可以获得给定个体的基因组的CNV的更准确的CNV注释。”哈佛医学院和杨百翰及妇女医院副教授查尔斯·李博士,研究人员之一。 “在这种情况下,我们开发并使用了由Agilent制造的定制的高分辨率CNV阵列集,其中包含2400万个寡核苷酸探针。很高兴看到类似的方法用于全面识别更多个体中的CNV。”

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