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Whole Genome Sequencing of Bilateral Cleft Lip and Palate Families from Africa: CIDR
Study
phs002623
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Kids First: The Genomic Basis of Structural Birth Defects Associated with Chromosome 18 Copy Number Changes
Study
phs002627
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Extrachromosomal DNA Amplification Contributes to Small Cell Lung Cancer Heterogeneity and is Associated with Worse Outcomes
Study
phs003190
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Kids First: Whole Genome Sequencing in Recessive Structural Brain Defects
Study
phs002590
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Experimental and Clinical Studies of Presbycusis
Study
phs003327
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Epigenetic Changes in Immune Response and Oncogenesis Related Genes Caused by Heavy Metal Long-Term Exposure
Study
phs003392
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PIEZO1 Loss of Function Compound Heterozygous Mutation in the Rare Congenital Human Disorder Prune Belly Syndrome
Study
phs003475
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Enhancing Open Data Sharing for Functional Genomics Experiments: Measures to Quantify Genomic Information Leakage and File Formats for Privacy Preservation
Study
phs003166
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Diabetes Multi-Omic Investigation of Drug Response (DIAMOND)
Study
phs003350
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Multi-Ethnic Study of Atherosclerosis (BioLINCC)
Study
phs003288