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Cancer-gene data sharing boosted

机译:癌症基因数据共享得到加强

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When the US diagnostics giant Myriad Genetics had its legal monopoly on breast-cancer gene testing eliminated one year ago, the company still retained an enormous edge over competitors. Although the US Supreme Courts ruling last June invalidated the patenting of genes, and with it Myriads exclusive rights on two genes associated with breast- and ovarian-cancer risk, the firm still has a private trove of data from 1.3 million genetic tests. That information gives Myriad, of Salt Lake City, Utah, an advantage in interpreting test results on these genes. But a coalition of scientists, physicians, patients and genetic counsellors says that it will soon eliminate that advantage. A year after the Supreme Court invalidated the patenting of genes - and with it, Myriad's monopoly on testing for mutations in the BRCA1 and BRCA2 genes linked to breast and ovarian cancer - the number of entries for BRCA variants in ClinVar, a public database for clinical genetic data, has grown to around one-third of the number in the Myriad database. Leaders of the public effort say that it is a showcase for how scientists can clear long-standing obstacles to sharing genetic information.
机译:一年前,当美国诊断巨人Myriad Genetics取消了对乳腺癌基因检测的法律垄断时,该公司仍然在竞争者中保持着巨大优势。尽管去年6月美国最高法院的裁决使基因的专利权无效,并且Myriads拥有与乳腺癌和卵巢癌风险相关的两个基因的专有权,但该公司仍然拥有130万个基因测试的私人数据。这些信息为犹他州盐湖城的Myriad提供了解释这些基因测试结果的优势。但是,由科学家,医师,患者和遗传咨询师组成的联盟表示,它将很快消除这种优势。最高法院宣布基因专利权无效一年后,Myriad垄断了与乳腺癌和卵巢癌相关的BRCA1和BRCA2基因突变检测的测试-临床公共数据库ClinVar中BRCA变体的条目数遗传数据已增长到Myriad数据库中数据的三分之一左右。公众努力的负责人说,这是科学家如何清除共享遗传信息的长期障碍的展示。

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  • 来源
    《Nature》 |2014年第7504期|198-198|共1页
  • 作者

    ERIKA CHECK HAYDEN;

  • 作者单位
  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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