首页> 美国卫生研究院文献>Genome Medicine >Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank

【2h】

Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank

机译：外显子组测序揭示了在以人群为基础的多样化生物库中BRCA1和BRCA2奠基者变异的普遍性

代理获取

本网站仅为用户提供外文OA文献查询和代理获取服务，本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文，但由于OA文献来源多样且变更频繁，仍可能出现获取不到、文献不完整或与标题不符等情况，如果获取不到我们将提供退款服务。请知悉。

页面导航

摘要
著录项
相似文献
相关主题

摘要

Demographics of exome-sequenced adult Bio Biobank participants and of individuals harboring expected pathogenic variants in

机译：外显子组测序的成人Bio Biobank参与者和具有预期病原体变异的个体的人口统计学

著录项

期刊名称 Genome Medicine
作者
Noura S. Abul-Husn; Emily R. Soper; Jacqueline A. Odgis; Sinead Cullina; Dean Bobo; Arden Moscati; Jessica E. Rodriguez; CBIPM Genomics Team; Regeneron Genetics Center; Ruth J. F. Loos; Judy H. Cho; Gillian M. Belbin; Sabrina A. Suckiel; Eimear E. Kenny;
展开▼
作者单位

展开▼
年(卷),期 2020(12),-1
年度 2020
页码 -1
总页数 12
原文格式 PDF
正文语种
中图分类生化遗传学;生化药理学;
关键词

相似文献

外文文献
中文文献
专利

1. Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank [J] . Noura S. Abul-Husn, Emily R. Soper, Jacqueline A. Odgis, Genome Medicine . 2020,第1期

机译：Exome测序显示BRCA1和BRCA2创始人变体在不同的基于人群的BIOBANK中的高患病率
2. Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families [J] . Rajendra Bahadur Shahi, Sylvia De Brakeleer, Ben Caljon, BMC Cancer . 2019,第1期

机译：通过对BRCA1和BRCA2阴性乳腺癌家族的指数患者进行全外壳测序来鉴定候选癌易腐烂的变体
3. Whole‐exome sequencing reveals novel genetic variants associated with diverse phenotypes of melanoma cells [J] . Hartman Mariusz L., Sztiller‐Sikorska Malgorzata, Czyz Malgorzata Molecular Carcinogenesis . 2019,第4期

机译：全末端测序揭示了与黑素瘤细胞不同表型相关的新型遗传变体
4. East Asian specific asthma associated variants were discovered via exome-sequencing [C] . Dankyu Yoon, Su-Jin Baek, Kipoong Kim, IEEE International Conference on Bioinformatics and Biomedicine . 2018

机译：通过外显子组测序发现与东亚特定哮喘相关的变异
5. Statistical Analysis of Genetic Sequence Variants in Whole Exome Sequencing Data from Patients with Prostate Cancer [D] . Ofori-Minta, Kelvin. 2021

机译：从前列腺癌患者的整个外壳测序数据中遗传序列变异的统计分析
6. Next Generation Sequencing Reveals High Prevalence of BRCA1 and BRCA2 Variants of Unknown Significance in Early-Onset Breast Cancer in African American Women [O] . Luisel Ricks-Santi, J. Tyson McDonald, Bert Gold, 2017

机译：下一代测序揭示了非洲裔美国女性早期乳腺癌中未知意义的BRCA1和BRCA2变异的高发生率
7. Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank [O] . Noura S. Abul-Husn, Emily R. Soper, Jacqueline A. Odgis, 2019

机译：Exome测序显示BRCA1和BRCA2创始人变体在不同的基于人群的BIOBANK中的高患病率

Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank

摘要

著录项

相似文献

相关主题

期刊订阅