A genome-wide approach to link genotype to clinical outcome by utilizing next generation sequencing and gene chip data of 6,697 breast cancer patients.
第一作者:
Lőrinc,Pongor
第一单位:
MTA TTK Lendület Cancer Biomarker Research Group, Research Centre for Natural Sciences, Magyar tudósok körútja 2, Budapest, H-1117, Hungary.;2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.
作者:
主题词
乳腺肿瘤(Breast Neoplasms);DNA拷贝数变异(DNA Copy Number Variations);女(雌)性(Female);基因组, 人(Genome, Human);基因型(Genotype);高通量核苷酸序列分析(High-Throughput Nucleotide Sequencing);人类(Humans);突变(Mutation);寡核苷酸序列分析(Oligonucleotide Array Sequence Analysis);序列分析, RNA(Sequence Analysis, RNA)
DOI
10.1186/s13073-015-0228-1
PMID
26474971
发布时间
2018-11-13
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Genome medicine
104页
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