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2022-01-14
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
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Copy number variation analysis of human Barrett's esophagus stem cells
This SuperSeries is composed of the SubSeries listed below. Refer to individual Series
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Genomic copy number alterations as predictive markers of systemic recurrence in breast cancer
Genomic copy number alterations as predictive markers of systemic recurrence in breast cancer
ChEBI2010-05-26 更新30
De novo copy number variations in cloned dogs (Illumina SNP)
De novo copy number variations in cloned dogs (Illumina SNP)
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Supplementary Table 5 from Comparative Study on the Efficacy and Exposure of Molecular Target Agents in Non–small Cell Lung Cancer PDX Models with Driver Genetic Alterations
Supplementary Table 5Copy number alteration result
Figshare2022-02-01 更新40
