Detection of genomic copy number variations induced by multiple DNA breaks
收藏Alliance of Genome Resources2026-08-01 收录
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Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity [GenomeWideSNP_6]
Purpose: Obesity is known to be a multifactorial condition that is highly heritable. There have been ~60 susceptibility loci identified, but they only account for a fraction of cases.. As copy number
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Clinically significant CNVs other than common aneuploidies detected in the first-tier test study with additional information provided by aCGH over karyotyping.
AF: amniotic fluid; ASD: atrial septal defect; CV: chorionic villi; DCDA: dichorionic diamniotic; DS: Down syndrome screening; FB: fetal blood; Gest: Gestation; IUGR: intrauterine growth restriction;
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Analysis of transgenerational effects on DNA copy number aberrations in male mice exposed to continuous 1mGy/day gamma-rays for 400 days (Primary screening for 1mGyA familly).. Analysis of transgenerational effects on DNA copy number aberrations in male mice exposed to continuous 1mGy/day gamma-rays for 400 days (Primary screening for 1mGyA familly).
Transgenerational effects of continuous low dose-rate (LDR) gamma-ray irradiation have not been well studied. Recent advances in DNA technology enabled us to examine a whole genome at molecular level.
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Additional file 7: Table S5. of Cribriform and intraductal prostate cancer are associated with increased genomic instability and distinct genomic alterations
Significant CNAs identified by logistic regression analysis accounting for genomic instability as confounding factor in the TCGA dataset. Columns contain: Symbol – official gene symbol, Chromosome / S
Figshare2018-01-03 更新20
