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The Transcriptional Landscape of SHH Medulloblastoma
Dataset
EGAD00001006305
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Somatic mutations reveal embryonic genetic bottlenecks generating placental mosaicism
Dataset
EGAD00001006337
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Pre-clinical evolution of haematological malignancies_WGS
Dataset
EGAD00001006423
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Measurable residual disease in elderly acute myeloid leukemia: results from the PETHEMA-FLUGAZA phase III clinical trial
Dataset
EGAD00001006585
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Expression profiles and genetic makeup of agnospheres.
Dataset
EGAD00001006668
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CINECA_synthetic_cohort_EUROPE_UK1 referencing fake samples
Dataset
EGAD00001006673
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Whole Exome sequencing data from Shwachman-Diamond syndrome bone marrow samples
Dataset
EGAD00001006815
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Dedifferentiated Melanoma (2021-02-02)
Dataset
EGAD00001006931
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Fetal origins of malignant germ cell tumours
Dataset
EGAD00001007038
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Genetic-epigenetic tissue mapping for plasma DNA: applications in prenatal testing, transplantation and oncology
Dataset
EGAD00001007041
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HV31 - Illumina PCR-free sequencing
Dataset
EGAD00001007042
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Genomic and transcriptomic landscape of T-cell lymphoblastic lymphoma compared to T-cell acute lymphoblastic leukemia: similar subtypes and different fusions
Dataset
EGAD00001015357
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Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015376
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Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015377
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Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyoma WES
Dataset
EGAD00001014787
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Clonal selection after gene therapy in sickle cell disease
Dataset
EGAD00001010914
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Clinical and genetic factors associated with tumor response to neoadjuvant (chemo)radiotherapy, survival and recurrence risk in rectal cancer
Dataset
EGAD00001011297
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An MTOR mutation hitchhikes through renal embryogenesis, driving multifocal, multiphenotypic tumours - RNA
Dataset
EGAD00001011646
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Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyosarcoma WES
Dataset
EGAD00001014789
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Exome sequencing of UK Birth Cohorts - Avon Longitudinal Study of Parents and Children
Dataset
EGAD00001015371
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Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015379
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Gene expression QTL mapping in stimulated iPSC-derived macrophages
Dataset
EGAD00001015380
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WES in pleural mesothelioma primary cell lines
Dataset
EGAD00001015409
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Selection of somatic escape variants in SERPINA1 in liver tissue of patients with alpha-1 anti-trypsin deficiency - Exome
Dataset
EGAD00001015431
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The earliest stages of neoplastic transformation in Familial Adenomatous Polyposis
Dataset
EGAD00001015471
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Single-Cell DNA Methylation Profiling via scTAMseq
Dataset
EGAD00001015498
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Whole-genome sequencing across 449 samples spanning 47 ethnolinguistic groups provides insights into genetic diversity in Nigeria
Study
EGAS00001007036
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Timing chromosomal amplification events using patterns of somatic mutations in high hyperdiploid acute lymphoblastic leukemia
Study
EGAS00001007052
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Ultrasensitive detection of minor allele fractions in maternal samples based on microhaplotype analysis
Study
EGAS00001007057
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Long-term organoid culture of a small intestinal neuroendocrine tumor rna-seq
Study
EGAS00001007108
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Effects of 2DG, Galactose, or Oligomycin on the epigenome remodeling induce by T cells activation.
Study
EGAS00001007115
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DERMATLAS__Leiomyosarcoma_WES
Study
EGAS00001007628
-
H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis
Study
EGAS00001007173
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Bacterial SNPs in the human gut microbiome associate with host BMI
Study
EGAS00001007204
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Genome-wide DNA Methylation Analysis Reveals a Unique Methylation Pattern for Pleural Mesothelioma Compared to Healthy Pleura and Other Lung Diseases
Study
EGAS00001007783
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A GWAS study with the AlpeDPD study cohort
Study
EGAS00001007855
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Genomic Landscape and Clonal Architecture in Pediatric Myeloid Neoplasms with Chromosome 7 Deletions
Study
EGAS00001008055
-
Spatiotemporal evolution and inter-patient heterogeneity in primary and recurrent/metastatic head and neck squamous cell carcinoma
Study
EGAS00001007464
-
Single cell transcriptomic landscape of pediatric B-cell acute lymphoblastic leukemia: dissection of transcriptional heterogeneity and B-cell developmental state
Study
EGAS00001007512
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Genomic profiling of IBC
Study
EGAS00001007520
-
Low-coverage whole genome sequencing for a highly selective cohort of severe COVID-19 patients
Study
EGAS00001007573
-
Comprehensive Deep Sequencing Atlas in HCC tumors
Study
EGAS00001007694
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DERMATLAS__Poroma_WES
Study
EGAS00001007705
-
Nala GSI GSAv3 PGx Study
Study
EGAS00001007710
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_WES
Study
EGAS00001007745
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_RNAseq
Study
EGAS00001007746
-
Ewing and Ewing-like-sarcoma tumoroid biobank reveals distinct drug sensitivities: translocation makes the difference
Study
EGAS00001007941
-
Double mutant DNMT3A AML: a unique subtype
Study
EGAS00001007966
-
Preclinical Pediatric Molecular Analysis for Therapy Choice (MATCH)
Study
EGAS00001008011
-
Whole exome and RNA sequencing of organoid samples derived from TRACERx patients
Study
EGAS00001008092