换一批Analyzing copy number variation using SNP array data: protocols for calling CNV and association tests.
第一作者：
Chiao-Feng,Lin
第一单位：
Department of Pathology and Laboratory Medicine and Institute for Biomedical Informatics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
作者：
医学主题词
算法(Algorithms);DNA拷贝数变异(DNA Copy Number Variations);基因频率(Gene Frequency);全基因组关联研究(Genome-Wide Association Study);高通量核苷酸序列分析(High-Throughput Nucleotide Sequencing);人类(Humans);寡核苷酸序列分析(Oligonucleotide Array Sequence Analysis);多态性, 单核苷酸(Polymorphism, Single Nucleotide)
DOI
10.1002/0471142905.hg0127s79
PMID
24510649
发布时间
2023-01-06
- 浏览18
Current protocols in human genetics
1.27.1-1.27.15页
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