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USU101 gene content determined by array CGH
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2014-08-18
相关数据集
Supplementary Material for: Application of Restriction Site-Associated DNA Sequencing (RAD-Seq) for Copy Number Variation and Triploidy Detection in Human
At present, low-pass whole-genome sequencing (WGS) is frequently used in clinical research and in the screening of copy number variations (CNVs). However, there are still some challenges in the detect
NIAID Data Ecosystem120
Tumor T6 Sectors
The following CGH experiments were conducted on four sectors (S1-S4) from a single primary ductal carcinoma tumor (T6) using the Sector-Ploidy-Profiling (SPP) Approach. SPP involves macro-dissecting
NIAID Data Ecosystem60
De novo copy number variations in cloned dogs (Illumina SNP)
De novo copy number variations in cloned dogs (Illumina SNP)
ChEBI2013-12-17 更新50
Additional file 4: of The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay
Childrenâs patients with two pathogenic/likely pathogenic CNVs. (XLSX 11 kb)
NIAID Data Ecosystem110
Additional file 4 of Copy number variation of microRNA genes in the human genome
Additional file 4:miRNAs located in CNVs with well defined breakpoints. Excel table showing characteristics of miRNAs located in CNVs with well defined breakpoints. (XLS 14 KB)
Figshare2020-08-27 更新50
