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Whole Exome Sequencing in Alopecia Areata Identifies Rare Mutations in KRT82
Study
phs002632
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Genetic Underpinnings of Ethnic Disparities in Bone Toxicities Between Hispanic and Non-Hispanic Children Treated for Acute Lymphoblastic Leukemia
Study
phs002317
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Genetic coupling of enhancer activity and connectivity in gene expression control
Study
EGAS50000000756
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Reference Exome Data for a Northern Brazilian population
Study
EGAS00001004112
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Onco-exaptation of an Endogenous Retroviral LTR Drives IRF5 Expression in Hodgkin Lymphoma
Study
EGAS00001001205
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Treatment-mediated selection of lethal prostate cancer clones defined by copy number architectures
Study
EGAS00001006598
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HLA-DR is absent in primitive macrophages through epigenetic silencing of master regulator CIITA
Study
EGAS00001006981
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Investigation of mutational signatures associated with DNMT3A deficiency (2019-04-03)
Dataset
EGAD00001004889
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16S-based fecal microbiota composition
Dataset
EGAD00001004979
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DNA whole-exome sequencing data from patients with metastatic basal cell carcinoma
Dataset
EGAD00001008675