Successful Coverage of Difficult to Sequence Genes (CALR, CEBPA, and FLT3) Associated with Myeloid Disorders Using a Hybridisation-Based Enrichment Approach Prior to Next-Generation Sequencing (NGS).

Georgieva L.; Uddin E.; Chan J.; Wright W.; Speight G.

首页> 外文期刊>The Journal of molecular diagnostics: JMD >Successful Coverage of Difficult to Sequence Genes (CALR, CEBPA, and FLT3) Associated with Myeloid Disorders Using a Hybridisation-Based Enrichment Approach Prior to Next-Generation Sequencing (NGS).

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Successful Coverage of Difficult to Sequence Genes (CALR, CEBPA, and FLT3) Associated with Myeloid Disorders Using a Hybridisation-Based Enrichment Approach Prior to Next-Generation Sequencing (NGS).

机译：在下一代测序（NGS）之前，使用杂交类富集方法（NGS）在下一代富集方法中成功覆盖与骨髓紊乱相关的序列基因（CALR，CEBPA和FLT3）。

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来源
《The Journal of molecular diagnostics: JMD》 |2017年第6期|共1页
作者
Georgieva L.; Uddin E.; Chan J.; Wright W.; Speight G.;
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Oxford Gene Technol Begbroke England;

Oxford Gene Technol Begbroke England;

Oxford Gene Technol Begbroke England;

Oxford Gene Technol Inc Tarrytown NY USA;

Oxford Gene Technol Begbroke England;

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正文语种 eng
中图分类临床医学;
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1. Successful Coverage of Difficult to Sequence Genes (CALR, CEBPA, and FLT3) Associated with Myeloid Disorders Using a Hybridisation-Based Enrichment Approach Prior to Next-Generation Sequencing (NGS). [J] . Georgieva L., Uddin E., Chan J., The Journal of molecular diagnostics: JMD . 2017,第6期

机译：在下一代测序（NGS）之前，使用杂交类富集方法（NGS）在下一代富集方法中成功覆盖与骨髓紊乱相关的序列基因（CALR，CEBPA和FLT3）。
2. The Application of a Hybridisation-Based Next-Generation Sequencing (NGS) Enrichment Panel for the Analysis of Key Genes Involved in Ovarian and Breast Tumours Using DNA From FFPE Samples [J] . Graham Speight, Jacqueline Chan, Sabine Eckert, Cancer genetics . 2017,第期

机译：基于杂交的下一代测序（NGS）富集面板用于分析来自FFPE样品的DNA参与卵巢肿瘤和乳腺肿瘤的关键基因
3. The Application of a Hybridisation-Based Next-Generation Sequencing (NGS) Enrichment Panel for the Analysis of Key Genes Involved in Ovarian and Breast Tumours Using DNA From FFPE Samples [J] . Graham Speight, Jacqueline Chan, Sabine Eckert, Cancer genetics . 2017,第期

机译：基于杂交的下一代测序（NGS）富集面板用于分析来自FFPE样品的DNA参与卵巢肿瘤和乳腺肿瘤的关键基因
4. A long PCR–based approach for DNA enrichment prior to next-generation sequencing for systematic studies [O] . Simon Uribe-Convers, Justin R. Duke, Michael J. Moore, 2014

机译：在下一代测序之前进行基于长PCR的DNA富集方法进行系统研究
5. Mutational spectrum of acute myeloid leukemia patients with double CEBPA mutations based on next-generation sequencing and its prognostic significance [O] . Long Su, YeHui Tan, Hai Lin, 2018

机译：基于下一代测序的双CeBPA突变患者的急性髓性白血病患者的突变谱及其预后意义

Successful Coverage of Difficult to Sequence Genes (CALR, CEBPA, and FLT3) Associated with Myeloid Disorders Using a Hybridisation-Based Enrichment Approach Prior to Next-Generation Sequencing (NGS).

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