官方服务:
资源简介:
Type I error rates of three CNV tests evaluated based on 5000 replications.
应用场景:
创建时间:
2020-05-04
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
Incentive-Compatible Critical Values
Statistically significant results are more rewarded than insignificant ones, so researchers have the incentive to pursue statistical significance. Such p-hacking reduces the informativeness of hypothe
NBER2022-01-01 更新60
Appendix B. Tables showing P values and power-simulation results for each of the 19 data sets.
Tables showing P values and power-simulation results for each of the 19 data sets.
DataCite Commons2025-06-01 更新50
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
VMR for genes with different duplication states. Shown is the average VMR for the whole genome, unique genes, segmental duplicated genes and tandem duplicated genes.
VMR for genes with different duplication states. Shown is the average VMR for the whole genome, unique genes, segmental duplicated genes and tandem duplicated genes.
NIAID Data Ecosystem60



