EVAapplication/xmlftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1348893/Control1.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1348893/CKD_Patient1.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1348893/CKD_Patient1.vcf.gz.csiftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1348893/Control1.vcf.gz.csiftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1348893/CKD_Patient.vcf.gz.csiftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1348893/Control.vcf.gz.csiftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1348893/Control.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1348893/CKD_Patient.vcf.gzftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1348893/CKD_Patient.vcf.csiftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1348893/CKD_Patient1.vcf.csiftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1348893/Control.vcf.csiftp://ftp.ebi.ac.uk/pub/databases/eva/PRJNA1348893/Control1.vcf.csiprimaryOK200Exome SequencingGenomicsMisr University for Science and Technology (MUST)Illumina NovaSeq 6000Homo Sapienshttps://www.ebi.ac.uk/eva/?eva-study=PRJNA1348893EVAfalseGenetic Analysis in Patients with Chronic Kidney Disease (CKD) and Healthy ControlsThis project involves Whole Exome Sequencing (WES) of human samples obtained from individuals diagnosed with Chronic Kidney Disease (CKD) and matched healthy control subjects. The goal of the study is to identify potentially pathogenic genetic variants that may contribute to CKD susceptibility, disease progression, and clinical phenotype variation. Comparative analysis between the CKD group and healthy controls enables the detection of disease-associated variants, rare mutations, and disrupted gene pathways.2025-11-06PRJNA13488939606