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Whole exome sequencing data of germline and two independent primary leukemias of five patients
Study
EGAS00001001889
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Expression-Based Subtypes Define Pathologic Response to Neoadjuvant Immune-Checkpoint Inhibitors in Muscle-Invasive Bladder Cancer
Study
EGAS00001005549
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Patient-derived neuroblastoma model system OHC-NB1
Study
EGAS00001003031
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Genomic History of the Solomon Islands
Study
EGAS00001006116
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WGS_of_healhy_mesothelial_cells_and_primary_mesothelima_cell_lines
Study
EGAS00001005559
-
Exome sequencing reveals pathogenic variants in known and novel candidate genes for severe sperm motility disorders
Study
EGAS00001005018
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Mitochondrial DNA sequencing of iPSC, parental cells, and iPSC derived cardiomyocytes
Study
EGAS00001005560
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Comprehensive pharmacogenomic characterization of gastric cancer
Study
EGAS00001004106
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SLC9A3R1 variant associated with age-related hearing loss
Study
EGAS00001003072
-
Ovarian cancer organoid biobank
Study
EGAS00001003073
-
Whole genome sequencing of a breast cancer cohort with known functional homologous recombination status
Study
EGAS00001005572
-
Germline elongator mutations in sonic hedgehog medulloblastoma
Study
EGAS00001004126
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Cancer immune control needs senescence induction by Stat1 dependent cell cycle regulator pathways in tumours
Study
EGAS00001004151
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Genetics and therapeutic responses to TIL therapy of pancreatic cancer PDX models
Study
EGAS00001005596
-
IVF Whole genome prediction
Study
EGAS00001005619
-
Characterization of DLBCL with a PMBL gene expression signature
Study
EGAS00001005057
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003137
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003139
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Germline biallelic mutation affecting the transcription factor Helios causes pleiotropic defects of immunity
Study
EGAS00001005675
-
Clonal evolution and clinical implications of genetic abnormalities in blastic transformation of chronic myeloid leukaemia
Study
EGAS00001005075
-
Comprehensive Genomic Characterization of Gene Therapy-Induced T-cell Acute Lymphoblastic Leukemia (H007)
Study
EGAS00001003870
-
Systematic comparative analysis of single-nucleotide variants detection methods from single-cell RNA sequencing data
Study
EGAS00001003883
-
Whole-exome sequencing of the transposition of the great arteries
Study
EGAS00001004175
-
Pediatric HGG WES and RNA-Seq
Study
EGAS00001005687
-
Comprehensive genetic analysis of Epstein-Barr virus-associated hematological malignancy
Study
EGAS00001003159