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资源简介：
aCGH raw data submitted to Gene Expression Omnibus
应用场景：
创建时间：
2015-01-01
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
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
Variant annotation in isolates serially passaged on media without antibiotic.
Variants were called against the NCBI PAO1 reference (RefSeq accession NC_002516.2) and annotated with snpEff. Annotation fields are as follows: LINEAGE = underlying genotype in first position (1 = MP
Figshare2022-11-18 更新40
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
