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Chromosomal changes in primary human uveal melanomas
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创建时间:
2012-12-06
相关数据集
Chromosomal status of GM00285 and GM05563 fibroblast and iPSCs. Homo sapiens
We generated induced pluripotent stem cells (iPSCs) from ring chromosome patients' cells. To examine chromosomal status in these iPSCs, we performed SNP microarray analysis using Agilent Sureprint G3
NIAID Data Ecosystem90
Highly correlated genes with BAP1 in the entire UVM dataset.
Highly correlated genes with BAP1 in the entire UVM dataset.
Figshare2019-02-04 更新50
Supplementary Material for: Impaired Spermatogenesis due to Small Supernumerary Marker Chromosomes: The Reason for Infertility Is Only Reliably Ascertainable by Cytogenetics
Infertile male with small supernumerary marker chromosomes (sSMCs) were studied. Overall, 37 own patients and 166 cases from the literature were included. sSMCs of our own cases were characterized by
Figshare2018-08-08 更新20
Array CGH analysis of human uveal melanomas. Array CGH analysis of human uveal melanomas
Primary uveal melanomas show multiple chromosomal aberrations. To identify genome variation in six human primary uveal melanomas, genome wide copy number variation (CNV) analyses were carried out in h
NIAID Data Ecosystem60
Comparison of clinical outcomes from baseline analysis of the two screening approaches in a general screening population.
NIPT, non-invasive prenatal testing * 70% of total affected pregnancies (30% receive no screening). † Assuming termination rates for trisomy 21, trisomy 18, trisomy 13, and monosomy X of 87%, 81%, 90%
NIAID Data Ecosystem40



