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Ethiopia_Genome_Project__high_coverage_
Study
EGAS00001000237
-
The Genomic Landscape of Core-Binding Factor Acute Myeloid Leukemias
Study
EGAS00001000349
-
Whole-exome and targeted sequencing of pediatric hyperdiploid B-cell precursor acute lymphoblastic leukemia
Study
EGAS00001001113
-
Whole genome, whole exome, and targeted sequencing of high-grade meningioma tumor samples.
Study
EGAS00001002294
-
Reconstituting the transcriptome and DNA methylome landscapes of human implantation at single-cell resolution
Study
EGAS00001003443
-
Ethiopia_Genome_Project__low_coverage_
Study
EGAS00001000238
-
Large-scale viral genome analysis identifies novel clinical associations between hepatitis B virus and chronically infected patients
Study
EGAS00001003689
-
The Prediction and Prevention of Preeclampsia
Study
EGAS00001001898
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities WGS
Study
EGAS00001006865
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities RNA-Seq
Study
EGAS00001006866
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities DNA-Methylation
Study
EGAS00001006881
-
Detection of cancers three years prior to diagnosis using plasma cell-free DNA
Study
EGAS00001008068
-
The Nordic Centre of Excellence Programme in Molecular Medicine Data Access Committee
Dac
EGAC00000000006
-
Expression-Based Subtypes Define Pathologic Response to Neoadjuvant Immune-Checkpoint Inhibitors in Muscle-Invasive Bladder Cancer
Dac
EGAC00001002276
-
EGAD00010000724
Dataset
EGAD00010000724
-
EGAD00010000474
Dataset
EGAD00010000474
-
EGAD00010000476
Dataset
EGAD00010000476
-
EGAD00010000478
Dataset
EGAD00010000478
-
Methylation differences in trisomy 21 using monozygotic twins - RRBS dataset
Dataset
EGAD00001001272
-
Identification of molecular subgroups in multiple myeloma by whole exome sequencing.
Dataset
EGAD00001004408
-
RHD_NC_OMNI_Cases
Dataset
EGAD00010000956
-
Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features
Study
EGAS00001005346
-
Somatic mutations in healthy and leukemic blood progenitors reveal evolutionary mechanisms underlying childhood leukemia and differential patient outcome
Study
EGAS00001004593
-
Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features
Study
EGAS00001005355
-
RNA sequencing of in vitro generated suppressive myeloid cells using parental and Sialidase expressing A549 cancer cell lines
Study
EGAS00001007618