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Copy number variants and overlapping genes associated with each region called in each cell line. (XLSX)
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2022-09-13
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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
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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
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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
Table_1_Multivariate piecewise linear regression model to predict radiosensitivity using the association with the genome-wide copy number variation.xlsx
IntroductionThe search for biomarkers to predict radiosensitivity is important not only to individualize radiotherapy of cancer patients but also to forecast radiation exposure risks. The aim of this
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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
