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Copy Number Variations (CNVs)
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2015-12-02
相关数据集
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (GenomeWideSNP_6). Homo sapiens
Systematic evaluation of eleven array platforms commonly used for CNV detection to address parameters of quality and CNV calling. Overall design: 36 Samples
NIAID Data Ecosystem60
Additional file 3 of Loqusdb: added value of an observations database of local genomic variation
Additional file 3 Table S2. SV variants filtered for major haplogroups. File is in csv format.
Figshare2020-07-02 更新40
Array segmentation methods.
Entries in the table indicate the proportion of times (out of 125 observations in each category) that top-down segmentation outperforms the bottom-up approach. Values smaller than (highlighted) indica
Figshare2015-12-02 更新30
Somatic CNV profile of congenital ectopic thyroids
To assess whether specific genes have relevant somatic genetic or epigenetic alterations in ectopic tissue, we used a combined analysis of transcriptome (confirmed by qRT-PCR on 68 genes), methylome,
NIAID Data Ecosystem60
Output from GRIMM showing the most parsimonious reversal scenario.
Each number represents an LCB calculated by MAUVE between CA88 and CO92. Changes between steps are underlined. Negative numbers represent an inverted LCB.
Figshare2015-12-02 更新30
