Performance Characteristics of a Targeted Sequencing Platform for Simultaneous Detection of Single Nucleotide Variants, Insertions/Deletions, Copy Number Alterations, and Gene Fusions in Cancer Genome.
第一作者:
Kyung,Park
第一单位:
From the Department of Pathology and Laboratory Medicine (Park, Marrero Rolon, Scognamiglio, Borczuk, Mosquera, Pan, Rubin, Rennert, Fernandes, Song), Weill Cornell Medicine, New York, New York.
作者:
医学主题词
DNA拷贝数变异(DNA Copy Number Variations);基因融合(Gene Fusion);遗传变异(Genetic Variation);高通量核苷酸序列分析(High-Throughput Nucleotide Sequencing);人类(Humans);诱变, 插入(Mutagenesis, Insertional);肿瘤(Neoplasms);多态性, 单核苷酸(Polymorphism, Single Nucleotide);结果可重复性(Reproducibility of Results);敏感性与特异性(Sensitivity and Specificity);序列分析, DNA(Sequence Analysis, DNA);序列缺失(Sequence Deletion)
DOI
10.5858/arpa.2019-0162-OA
PMID
32045275
发布时间
2021-01-11
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