相关数据集
WES of 3 Relapsed ALK+ ALCL PDX
Whole-exome sequencing (WES) of high-risk paediatric/young adult ALK+ ALCL PDX, for three patients who underwent relapse, and WES of corresponding diagnostic and germline tissue where available.
NIAID Data Ecosystem30
Additional file 13: Table S10. of A unified analytic framework for prioritization of non-coding variants of uncertain significance in heritable breast and ovarian cancer
Prioritized Variants by Gene (XLSX 16Â kb)
Figshare2016-12-16 更新20
Additional file 16 of Prevalence and impact of molecular variation in the three-prime repair exonuclease 1 TREX1 and its implications for oncology
Additional file 16. Table S13. Distribution of different nucleotide sequence variant categories in TCGA cancer histologies.
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Table1_Rare copy number variation analysis identifies disease-related variants in atrioventricular septal defect patients.XLSX
Atrioventricular septal defect (AVSD) is a deleterious subtype of congenital heart diseases (CHD) characterized by atrioventricular canal defect. The pathogenic genetic changes of AVSD remain elusive,
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Burden analysis of EBAV CNVs.
Bicuspid aortic valve (BAV), the most common congenital heart defect, is a major cause of aortic valve disease requiring valve interventions and thoracic aortic aneurysms predisposing to acute aortic
NIAID Data Ecosystem20
