官方服务：
资源简介：
GenomEUtwin Finnish (FIN) samplesEGA dataset EGAD00000000042
应用场景：
创建时间：
2019-10-01
相关数据集
Early post-zygotic mutations contribute to de novo variation in a healthy monozygotic twin pair
Background Human de novo single nucleotide variation (SNV) rate is estimated to range between 0.84 â 3 Ã 10-8 mutations per base per generation. However, contribution of early post-zygotic mutation
NIAID Data Ecosystem90
Additional file 1 of Transition of allele-specific DNA hydroxymethylation at regulatory loci is associated with phenotypic variation in monozygotic twins discordant for psychiatric disorders
Additional file 1: Table S1. Summary of 5hmC-seq and WGS data for each twin pair. Table S2. Primers and probes employed in this study. Table S3. The number of AShM sites identified in MZ twins. Table
NIAID Data Ecosystem40
A_study_of_Methylated_DNA_regions_in_Twins_. A_study_of_Methylated_DNA_regions_in_Twins_
DNA methylation is essential for normal development and has been implicated in many pathologies including cancer. Our knowledge about genome-wide distribution of DNA methylation how it changes during
NIAID Data Ecosystem40
Investigation of somatic copy number variation in MZ twins. Homo sapiens
There is growing evidence that genomic DNA sequence changes occur in individual somatic cells during the lifetime of an individual and accumulation of these changes may influence aging and disease. In
NIAID Data Ecosystem10
