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An efficient and comprehensive strategy for genetic diagnostics of polycystic kidney disease
Study
EGAS00001001003
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Germline and somatic SMARCA4 mutations characterize small-cell carcinoma of the ovary, hypercalcemic type.
Study
EGAS00001000721
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Malignant mesothelioma EWAS on European prospective study
Study
EGAS00001006432
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Genetic landscape of pediatric ETV6-RUNX1 acute lymphoblastic leukemia
Study
EGAS00001001314
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Genetic landscape of pediatric ETV6-RUNX1 acute lymphoblastic leukemia
Study
EGAS00001001315
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Study the genetic susceptibility of esophagus squamous cell carcinomas (ESCC) in high-risk area Henan Chinese
Study
EGAS00001003423
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Functional analysis of GATA2 synonymous mutations
Study
EGAS00001003817
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HLF COPD DNA Methylomics
Study
EGAS00001006603
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Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci
Study
EGAS00001002592
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Detecting PKD1 variants in Polycystic Kidney Disease patients by single-molecule long-read sequencing
Study
EGAS00001002106
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Epigenetic dynamics of monocyte to macrophage differentiation
Study
EGAS00001001595
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The subclonal architecture of metastatic breast cancer: Results from a prospective community-based rapid autopsy program 'CASCADE'
Study
EGAS00001002153
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Case Report: early contribution of germline and nevi genetic alterations to a rapidly-progressing Cutaneous Melanoma Patient
Study
EGAS00001006459
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Genomic landscape of oral cancers (Complete Genomics WGS)
Study
EGAS00001002393
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Population Structure and Genetic Diversity in Argentinean populations
Study
EGAS00001001663
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Comparison of HCC cell lines and primary HCCs
Study
EGAS00001001678
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BLUEPRINT Hematopoietic Stem/Progenitor Cell Methylomes
Study
EGAS00001002070
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Differential Presence of Exons in Cell-Free DNA Reveals Different Patterns in Colorectal Cancer Between Metastatic and Non-Metastatic Patients
Study
EGAS00001002687
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Whole-exome sequencing of breast cancer metastasis and corresponding blood samples
Study
EGAS00001001695
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Whole exome sequencing data for patients with Bosma arhinia microphthalmia syndrome (BAMS).
Study
EGAS00001002193
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Same-day genomic and epigenomic diagnosis of brain tumors using realtime nanopore sequencing
Study
EGAS00001002213
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DNA methylomes of monozygotic twins clinically discordant for multiple sclerosis
Study
EGAS00001003147
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Genetic sequencing of MODY patients.
Study
EGAS00001001699
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Whole exome sequencing of 76 individuals with familial atrial fibrillation
Study
EGAS00001003207
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Genomic profiling of esthesioneuroblastoma
Study
EGAS00001003225
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Genomic landscape of oral cancers (Illumina RNA-Seq)
Study
EGAS00001003237
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Genetic alterations in metastatic uveal melanoma
Study
EGAS00001003303
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Inherited genetic predisposition to childhood acute lymphoblastic leukemia investigated using a genome wide association study.
Study
EGAS00001002809
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Genome-wide DNA methylation profiles of NSCLC xenograft and primary lung tissues for the identification of epigenetic predictive biomarkers.
Study
EGAS00001002479
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Cryptic Relatedness in the Singapore Living Biobank Project
Study
EGAS00001002619
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Genomic Profiling Reveals Spatial Intra-tumour Heterogeneity in Follicular Lymphoma
Study
EGAS00001002492
-
Genetic and expression landscape of Waldenstrom macroglobulinemia
Study
EGAS00001003603
-
Phylogenetic evolution of metastatic melanoma.
Study
EGAS00001003582
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Genetic Basis of Hepatosplenic T Cell Lymphoma (HSTL)
Study
EGAS00001002182
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Combined genetic and transcriptome analysis of patients with Systemic Lupus Erythematosus (SLE)
Study
EGAS00001003662
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Whole-Exome Sequencing of Salivary Gland Mucoepidermoid Carcinoma
Study
EGAS00001002811
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Genomic characterization of esophageal squamous cell carcinoma reveals critical genes underlying tumorigenesis and poor prognosis
Study
EGAS00001001723
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Physiological and genetic adaptations to diving in Sea Nomads
Study
EGAS00001002823
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Cistrome-partitioning reveals convergence of somatic mutations and risk-variants on master transcription regulators in primary prostate tumors
Study
EGAS00001003928
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Whole-exome sequencing of the transposition of the great arteries
Study
EGAS00001004175
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Exome-sequencing of two UFM individuals and their Fragile X family members.
Study
EGAS00001001737
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InsPIRE islets
Study
EGAS00001003997
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Whole Exome Sequencing of Spanish Patients diagnosed with rare ophtalmogenetic disorders: Macular Dystrophy, Retinitis Pigmentosa and Leber's congenital amaurosis.
Study
EGAS00001004084
-
UCSF Pediatric Bithalamic Glioma Genome Project
Study
EGAS00001004033
-
An integrative model of pathway convergence in genetically heterogeneous blast crisis chronic myeloid leukemia (CML)
Study
EGAS00001001751
-
Dissection of the molecular complexity of colorectal cancer in pre-clinical models identifies predictive signatures of sensitivity to EGFR inhibitors
Study
EGAS00001001752
-
High-resolution analyses of human sperm dynamic methylome reveals thousands of novel age-related epigenetic alterations
Study
EGAS00001004168
-
Sex-biased patterns shaped the genetic history of Roma
Study
EGAS00001004207
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Expression-Based Subtypes Define Pathologic Response to Neoadjuvant Immune-Checkpoint Inhibitors in Muscle-Invasive Bladder Cancer
Study
EGAS00001005549
-
Ashkenazi Jewish Leukoencephalopathy
Study
EGAS00001001767