DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly.
第一作者:
Ilari,Scheinin
第一单位:
Department of Pathology, VU University Medical Center, 1007 MB Amsterdam, The Netherlands; Department of Pathology, Haartman Institute and HUSLAB, FIN-00014 University of Helsinki and Helsinki University Central Hospital, Helsinki, Finland;
作者:
主题词
算法(Algorithms);碱基组成(Base Composition);细胞系, 肿瘤(Cell Line, Tumor);比较基因组杂交(Comparative Genomic Hybridization);计算生物学(Computational Biology);DNA拷贝数变异(DNA Copy Number Variations);基因组, 人(Genome, Human);基因组学(Genomics);高通量核苷酸序列分析(High-Throughput Nucleotide Sequencing);人类(Humans);肿瘤(Neoplasms);软件(Software)
DOI
10.1101/gr.175141.114
PMID
25236618
发布时间
2022-11-09
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Genome research
2022-32页
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