Concurrent Detection of Target Copy Number Variants and Gene Variants (SNV/indels) in CLL Samples Using a Next-Generation Sequencing Panel

Georgieva L.; Uddin E.; Heckel A.; Pullabhatla V.; Reid J.; Speight G.

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Concurrent Detection of Target Copy Number Variants and Gene Variants (SNV/indels) in CLL Samples Using a Next-Generation Sequencing Panel

机译：使用下一代测序面板并发检测CLL样品中的目标拷贝数变体和基因变体（SNV / Indels）

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《The Journal of molecular diagnostics: JMD》 |2019年第6期|共1页
作者
Georgieva L.; Uddin E.; Heckel A.; Pullabhatla V.; Reid J.; Speight G.;
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Oxford Gene Technol Begbroke Oxon England;

Oxford Gene Technol Begbroke Oxon England;

Oxford Gene Technol Tarrytown NY USA;

Oxford Gene Technol Begbroke Oxon England;

Oxford Gene Technol Begbroke Oxon England;

Oxford Gene Technol Begbroke Oxon England;

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正文语种 eng
中图分类临床医学;
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1. Concurrent Detection of Target Copy Number Variants and Gene Variants (SNV/indels) in CLL Samples Using a Next-Generation Sequencing Panel [J] . Georgieva L., Uddin E., Heckel A., The Journal of molecular diagnostics: JMD . 2019,第6期

机译：使用下一代测序面板并发检测CLL样品中的目标拷贝数变体和基因变体（SNV / Indels）
2. Clinical Validation of a Comprehensive DNA/RNA Panel (170 Genes) for Single Nucleotide Variants (SNVs), Small Insertions/Deletions (Indels), Copy Number Variations (CNVs) Splice Variations (SVs), and Gene Fusions (GF) on an NGS Platform in a CLIA Setting. [J] . Kolhe R., Mondal A. K., Pundkar C., The Journal of molecular diagnostics: JMD . 2018,第6期

机译：单个核苷酸变体（SNV），小插入/缺失（诱导），拷贝数变异（CNV）剪切变异（SVS）和基因融合（GF）对NGS的临床验证平台在Clia设置。
3. Utility of a Comprehensive and Cost-effective DNA/RNA Panel (170 Genes) for Single Nucleotide Variants (SNV's), Small Insertions or Deletions (Indels), Copy Number Variations (CNV's) Splice Variations, and Gene Fusions on an NGS in Evaluation of Colon Cancer [J] . Kolhe R., Mondal A. K., Pundkar C., The Journal of molecular diagnostics: JMD . 2018,第6期

机译：用于单核苷酸变体（SNV），小插入或缺失（Indels），拷贝数变异（CNV）剪接变异和基因融合在评估中结肠癌
4. Sparse signal recovery methods for variant detection in next-generation sequencing data [C] . Mario Banuelos, Rubi Almanza, Lasith Adhikari, IEEE International Conference on Acoustics, Speech and Signal Processing . 2016

机译：用于下一代测序数据中变异检测的稀疏信号恢复方法
5. A Modified Information Criterion in the 1d Fused Lasso for DNA Copy Number Variant Detection using Next Generation Sequencing Data [D] . Lee, Jaeeun. 2017

机译：使用下一代测序数据的1d融合套索中用于DNA拷贝数变异检测的修正信息标准
6. Guideline-Adherent Clinical Validation of a Comprehensive 170-Gene DNA/RNA Panel for Determination of Small Variants Copy Number Variations Splice Variants and Fusions on a Next-Generation Sequencing Platform in the CLIA Setting [O] . Theresa A. Boyle, Ashis K. Mondal, Daryoush Saeed-Vafa, 2021

机译：综合170-基因DNA / RNA面板的指导鉴定临床验证用于测定CLIA设置下一代测序平台上的小变体拷贝数变异剪接变体和融合
7. Clinical Validation of Copy Number Variant Detection from Targeted Next-Generation Sequencing Panels [O] . Jennifer Kerkhof, Laila C. Schenkel, Jack Reilly, 2017

机译：目标下一代测序面板拷贝数变体检测的临床验证

Concurrent Detection of Target Copy Number Variants and Gene Variants (SNV/indels) in CLL Samples Using a Next-Generation Sequencing Panel

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