Identification of Germline Variants in Tumor Genomic Sequencing Assays: Usefulness of Variant Allele Fraction and Population Variant Databases

Montgomery N. D.; Selitsky S. R.; Patel N. M.; Hayes D. N.; Parker J. S.; Weck K. E.

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Identification of Germline Variants in Tumor Genomic Sequencing Assays: Usefulness of Variant Allele Fraction and Population Variant Databases

机译：肿瘤基因组测序测定中种系变体的鉴定：变异等位基因分数和人口变异数据库的有用性

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来源
《The Journal of molecular diagnostics: JMD》 |2017年第6期|共2页
作者
Montgomery N. D.; Selitsky S. R.; Patel N. M.; Hayes D. N.; Parker J. S.; Weck K. E.;
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作者单位

Univ N Carolina Sch Med Chapel Hill NC USA;

Univ N Carolina Sch Med Chapel Hill NC USA;

Univ N Carolina Sch Med Chapel Hill NC USA;

Univ N Carolina Sch Med Chapel Hill NC USA;

Univ N Carolina Sch Med Chapel Hill NC USA;

Univ N Carolina Sch Med Chapel Hill NC USA;

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原文格式 PDF
正文语种 eng
中图分类临床医学;
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1. Identification of Germline Variants in Tumor Genomic Sequencing Assays: Usefulness of Variant Allele Fraction and Population Variant Databases [J] . Montgomery N. D., Selitsky S. R., Patel N. M., The Journal of molecular diagnostics: JMD . 2017,第6期

机译：肿瘤基因组测序测定中种系变体的鉴定：变异等位基因分数和人口变异数据库的有用性
2. Identification of Germline Variants in Tumor Genomic Sequencing Analysis [J] . Montgomery Nathan D., Selitsky Sara R., Patel Nirali M., The Journal of molecular diagnostics: JMD . 2018,第1期

机译：肿瘤基因组测序分析中种系变体的鉴定
3. Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller [J] . Chang Xu, Mohammad R. Nezami Ranjbar, Zhong Wu, BMC Genomics . 2017,第1期

机译：使用靶向的DNA测序和新型的分子条形码识别变体调用程序来检测非常低的等位基因片段变体
4. Influence of XPD variant alleles on p53 mutations in lung tumors of nonsmokers and smokers [C] . Sai-Mei Hou, Annamaria Kannio, Sabrina Angelini, International Symposium of Radiation and Homeostasis . 2002

机译：XPD变异等位基因对非摩托车肺肿瘤P53突变的影响
5. Analysis of variant alleles of gene thought to affect breast cancer in a patient population from South Carolina. [D] . Occean, Amerline. 2010

机译：对南卡罗来纳州患者人群中可能影响乳腺癌的基因变异等位基因进行分析。
6. Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller [O] . Chang Xu, Mohammad R. Nezami Ranjbar, Zhong Wu, 2017

机译：使用靶向DNA测序和新型分子条形码识别变体调用程序检测非常低的等位基因片段变体
7. Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller [O] . Chang Xu, Mohammad R. Nezami Ranjbar, Zhong Wu, 2017

机译：使用靶向DNA测序和新型分子条形码识别变体调用程序检测非常低的等位基因片段变体

Identification of Germline Variants in Tumor Genomic Sequencing Assays: Usefulness of Variant Allele Fraction and Population Variant Databases

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