Copy number variation of UPF3B patients
收藏Research Data Australia2024-12-14 收录
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https://researchdata.edu.au/copy-number-variation-upf3b-patients/60541
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资源简介：
To assess the impact of UPF3B-NMD deficiency on human transcriptome, we overlapped identified differently expressed genes with copy number variation data of the patients, obtained using Illumina Human Omniexpress chip, to exclude possible false positive.
提供机构：
The University of Adelaide
