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Copy number alterations of 317 HNSCCs
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创建时间：
2021-04-16
相关数据集
Additional file 7: of Copy number variations in Friesian horses and genetic risk factors for insect bite hypersensitivity
5350 CNVRs detected by CNVRuler based on 15,041 CNVs identified by PennCNV in 222 Friesian horses. 5350 CNVRs detected by CNVRuler based on 15,041 CNVs identified in PennCNV [33â 35] in 222 Friesian h
Figshare2018-07-31 更新70
Table_3_The Landscape of Somatic Copy Number Alterations in Head and Neck Squamous Cell Carcinoma.XLS
Head and neck squamous cell carcinoma (HNSCC) is the sixth most common malignancy worldwide. Somatic copy number alterations (CNAs) play a significant role in the development of this lethal cancer. In
NIAID Data Ecosystem50
Common copy number variations overlapping with CNVs region known to be associated with breast cancer risk.
Common copy number variations overlapping with CNVs region known to be associated with breast cancer risk.
Figshare2021-01-27 更新10
Genome-wide copy number analyses reveal genomic abnormalities involved in transformation of follicular lymphoma. Genome-wide copy number analyses reveal genomic abnormalities involved in transformation of follicular lymphoma
This SuperSeries is composed of the SubSeries listed below. Overall design: Refer to individual Series
NIAID Data Ecosystem50
Table1_Analysis of Genomic Copy Number Variation in Miscarriages During Early and Middle Pregnancy.docx
The purpose of this study was to explore the copy number variations (CNVs) associated with miscarriage during early and middle pregnancy and provide useful genetic guidance for pregnancy and prenatal
NIAID Data Ecosystem10
