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HipSci HumanHT 12 Expression BeadChip analysis - Primary immune deficiency
Study
EGAS00001002027
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HipSci HumanHT 12 Expression BeadChip analysis - Bleeding and Platelet disorders
Study
EGAS00001002028
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DNA sequencing for human normal endometrial glands
Study
EGAS00001005822
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Gene regulation of human stimulated and cultured CD4+ Treg cells
Study
EGAS00001003515
-
Population_based_analysis_of_POT1_variants_in_a_cutaneous_melanoma_case_control_cohort
Study
EGAS00001006870
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Heterogeneous metabolic signatures are linked to cancer cell differentiation in colorectal cancer
Dataset
EGAD00001005524
-
Pre-neoplastic somatic mutations including MYD88L265P in lymphoplasmacytic lymphoma
Dataset
EGAD00001008196
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Colorectal cancer organoid-stroma biobank cohort
Dataset
EGAD00001011173
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Identifying autosomal recessive mutations causing neurological disorders
Dataset
EGAD00001000340
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Action to Control Cardiovascular Risk in Diabetes (ACCORD - Imaging)
Study
phs003562
-
Multiomics characterisation of the response to stimulation in Long Covid patients
Dataset
EGAD50000000203
-
Study on longer adjuvant chemotherapy in Women with Early Breast Cancer
Study
phs000807
-
Transdisciplinary Studies of Genetic Variation in Colorectal Cancer(CORECT): Axiom GWAS
Study
phs001856
-
Study of Leukemia Stem Cells in B-ALL
Study
phs002492
-
Whole-Genome and Exome Sequencing in clear-cell Renal Cell Carcinoma (ccRCC)
Study
phs000491
-
Loss of RREB1 in pancreatic beta cells reduces cellular insulin content and affects endocrine cell gene expression
Dataset
EGAD50000000515
-
cfRRBS methylation profiling of cfDNA from cerebrospinal fluid from pediatric CNS tumor patients
Dataset
EGAD50000000554
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Sex Differences in MAGEL2 Gene Promoter Methylation in High Functioning Autism - Trends from a Pilot Study Using Nanopore Cas9 Targeted Long Read Sequencing
Dataset
EGAD50000000726
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Genome-wide association scan in Parkinson's disease
Study
EGAS00000000034
-
Transplant Outcomes in Aplastic Anemia (TOAA): GWAS and Whole Exome Sequence Data
Study
phs001710
-
Determinants of DNA methylation patterning in human placental development and trophoblast stem cell models.
Study
EGAS50000000661
-
Detection of a recently described pre-T cell receptor-alpha immunodeficiency exclusively using whole genome sequencing
Dataset
EGAD50000000866
-
Application of organoid culture system of human gastrointestinal and thoracic cancer in genome medicine
Study
JGAS000664
-
Application of organoid culture system of human gastrointestinal and thoracic cancer in genome medicine
Study
JGAS000641
-
Application of organoid culture system of human gastrointestinal and thoracic cancer in genome medicine
Study
JGAS000653
-
Molecular profiling of HGBCL-DH-BCL2 patients treated in the HOVON-152 trial
Study
EGAS50000001453
-
Development of actionable molecular targets and/or biomarkers for prognostication and patient stratification in gynecological cancer based on whole-exome sequencing and epigenomic analysis
Study
JGAS000174
-
Screening of 2.5 million SNPs in 142 samples from the western Mediterranean area
Study
EGAS00001003901
-
End structure of DNA in plasma: detection, characterizationand diagnostic applications
Study
EGAS00001004080
-
Landscape of gene mutations in Down syndrome-related myeloid disorders
Study
EGAS00001000546
-
BLUEPRINT RNA-seq data for rare cells in the haematopoietic lineages, from adult and cord blood samples.
Study
EGAS00001000284
-
Nucleosome footprinting in plasma cell-free DNA for diagnosis of ovarian cancer
Study
EGAS00001005361
-
Advanced molecular neuropathology to increase diagnostic accuracy in pediatric neurooncology
Study
EGAS00001006680
-
WES on tumor DNA and germline DNA in pediatric cancer
Study
EGAS00001005429
-
DNA-seq FASTQ files from 16 carriers of the BMPR2 p.Arg491Gln mutation in a family affected by HPAH
Dataset
EGAD00001005756
-
Somatic mutation and clonal evolution in premalignant lung disease
Dataset
EGAD00001010122
-
A living biobank of patient-derived ductal carcinoma in situ Mouse-INtraDuctal xenografts identifies factors associated with risk of invasive progression
Dataset
EGAD00001009336
-
Somatic mutation and clonal evolution in the human bladder WES-NOVASEQ (2020-05-05)
Dataset
EGAD00001006117
-
Somatic mutation and clonal evolution in the human pancreas - WGS (2019-12-17)
Dataset
EGAD00001005751
-
WES of germline, nevi, primary and metastatic Cutaneous Melanoma from patient 009 in CASVAC-0401 trial
Dataset
EGAD00001009083
-
LSC RNA-Sequencing
Dataset
EGAD00001008488
-
two tables containing RNASeq expression values to patients with RNA-Seq data in the study "Comprehensive genomic characterization of refractory multiple myeloma (H067)"
Dataset
EGAD00001008363
-
Chromatin accessability in cytokine induced immune cell states (2019-03-19)
Dataset
EGAD00001004852
-
Epigenetic dysregulation in autism spectrum disorder
Dataset
EGAD00001002725
-
Genetic vulnerability of knockout cancer lines (2019-04-01)
Dataset
EGAD00001004881
-
ATAC-seq data from primary AML samples with t(3;8)
Dataset
EGAD00001007910
-
Chromatin accessability in cytokine induced immune cell states (2019-03-11)
Dataset
EGAD00001004831
-
RNAseq Iron-Treated iPSC-derived Microglia
Dataset
EGAD00001008660
-
Single cell transcriptomes of in vitro differentiated hepatocyte-like cells in comparison to primary human hepatocytes
Dataset
EGAD00001005946
-
Genetic determinants of monocyte splicing are enriched for disease susceptibility loci including for COVID-19
Dataset
EGAD00001010176