X chromosome-specific Array-CGH of XLMR patient
收藏官方服务:
资源简介:
X chromosome-specific Array-CGH of XLMR patient
应用场景:
创建时间:
2010-06-25
相关数据集
Table_1_Expanding the Scope of Non-invasive Prenatal Testing to Detect Fetal Chromosomal Copy Number Variations.xlsx
Non-invasive prenatal testing (NIPT) for common fetal trisomies is effective. However, the usefulness of cell-free DNA testing to detect other chromosomal abnormalities is poorly understood. We analyz
NIAID Data Ecosystem40
Additional file 3: of Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia
All rare (
DataCite Commons2020-08-31 更新30
Additional file 2: of Mapping the landscape of tandem repeat variability by targeted long read single molecule sequencing in familial X-linked intellectual disability
SureSelect capture probe design and information on the performance of the different probe combinations per target. (XLSX 1353 kb)
Figshare2018-12-20 更新20
Monosomy 3 and chromosome 8 copy number variation: SNP array versus dPCR analysis.
SNP and dPCR thresholds: loss, 2.1- 3.1* Aberration at chromosome 5, location of TERT, no proper correction possible with TERT dPCR Karyotype chromosome 3: 0; Disomy, 1; MonosomyKaryotype chromosome 8
Figshare2015-12-03 更新30
CGH array for human cell lines. Homo sapiens strain:HEK293T, HeLa, PC9
To determine chromosome copy number in HEK293T, HeLa and PC9 cells, CGH array analysis was performed using WTC11 iPS cells (normal diploid cells) as controls.
NIAID Data Ecosystem20



