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Tocilizumab treatment leads to early resolution of myeloid dysfunction and lymphopenia in patients hospitalized with COVID-19
Study
EGAS00001006688
-
GRIDSS, PURPLE, LINX: Unscrambling the tumor genome via integrated analysis of structural variation and copy number
Study
EGAS00001004034
-
The landscape of chromothripsis across adult cancer types
Study
EGAS00001004250
-
The Genetic Landscape of Ocular Adnexa MALT Lymphoma Reveals Frequent Aberrations in NFAT and MEF2B Signaling Pathways
Study
EGAS00001006631
-
Multi-omics identify falling LRRC15 as a COVID-19 severity marker and persistent pro-thrombotic signals in convalescence
Study
EGAS00001006778
-
Single-cell atlas of multiple myeloma and precursor diseases
Study
EGAS00001006694
-
Malignant progression of an ancestral bone marrow clone harboring a CIC-NUTM2A fusion in isolated myeloid sarcoma
Study
EGAS00001006833
-
WGS of MAPKi acquired resistant samples from patients and PDX models
Study
EGAS00001006874
-
Blood transcriptome profiling links immunity to disease severity in myotonic dystrophy type 1 (DM1).
Study
EGAS00001006926
-
Multiome_HB
Study
EGAS00001006932
-
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Study
EGAS00001006945
-
Single-cell RNA-seq and spatial transcriptomics data for the sarcoidosis baseline project
Study
EGAS00001006970
-
Neuroblastoma heterogeneity
Study
EGAS00001007016
-
Neuroblastoma heterogeneity
Study
EGAS00001007019
-
Single-cell RNA-seq of cervix and placenta
Study
EGAS00001007044
-
Epigenetic landscape of mixed phenotype leukemias
Study
EGAS00001007094
-
Integrative genomic analyses in adipocytes implicate DNA methylation in human obesity and diabetes
Study
EGAS00001007118
-
Spatial and temporal transcriptomics of medulloblastoma with chromothripsis identifies multiple genetic clones that resist to treatment and lead to relapse
Study
EGAS00001007128
-
Transcriptomic classes of BCR-ABL1 lymphoblastic leukemia
Study
EGAS00001007167
-
The genetic history of the southern Andes from present-day Mapuche ancestry
Study
EGAS00001007200
-
Single molecule genome-wide mutation profiles of cell-free DNA for non-invasive detection of cancer
Study
EGAS00001007248
-
An isogenic human iPSC model unravels neurodevelopmental abnormalities in SMA
Study
EGAS00001007259
-
RNAseq of Colorectal cancer organoid-stroma biobank cohort
Study
EGAS00001007300
-
WES of Colorectal cancer organoid-stroma biobank cohort
Study
EGAS00001007301
-
A longitudinal single-cell atlas of treatment response in pediatric AML
Study
EGAS00001007323
-
High-resolution, patient-level dissection of IL-23 blockade in cutaneous psoriasis
Study
EGAS00001007373
-
Immune landscape of oncohistone-mutant gliomas reveals diverse myeloid populations and tumor-promoting behavior
Study
EGAS00001007510
-
A clinically applicable connectivity signature for glioblastoma includes the tumor network driver CHI3L1
Study
EGAS00001007611
-
Early evolutionary branching across spatial domains predisposes to clonal replacement under chemotherapy in neuroblastoma
Study
EGAS00001007650
-
Repli-seq data for 'Replication timing alterations are associated with mutation acquisition during tumour evolution in breast and lung cancer'
Study
EGAS00001007773
-
Myeloid-specific KDM6B inhibition sensitizes Glioblastoma to PD1 blockade
Study
EGAS00001007002
-
Mutational Mechanisms in Multiply Relapsed Pediatric Acute Lymphoblastic Leukemia
Study
EGAS00001007900
-
Mapping the human hematopoietic stem and progenitor cell hierarchy through integrated single-cell proteomics and transcriptomics
Study
EGAS00001007930
-
Novel paediatric case of a spinal high-grade astrocytoma with piloid features in a patient with Noonan Syndrome
Study
EGAS00001007937
-
Cross-species Comparison Reveals Therapeutic Vulnerabilities Halting Glioblastoma Progression
Study
EGAS00001008155
-
Molecular and clinical diversity in primary central nervous system lymphoma: a LOC network multi-omic PCNSL study
Dataset
EGAD00001008706
-
RaScALL: Rapid (Ra) screening (Sc) of RNA-seq data for prognostically significant genomic alterations in acute lymphoblastic leukaemia (ALL)
Dataset
EGAD00001009087
-
Diagnostic utility of whole genome sequencing in adults with B-other acute lymphoblastic leukemia
Dataset
EGAD00001009304
-
Recurrent DNMT3B gene rearrangements are associated with unfavorable outcome in dicentric (9;20)-positive pediatric BCP-ALL
Dataset
EGAD00001011122
-
Comparison of sequencing assays for sensitive detection of circulating tumour DNA in stage IA-IV breast cancer
Dataset
EGAD00001008589
-
Mutation analysis of core biopsies from localized breast cancer patients
Dataset
EGAD00001008396
-
ANGIOPREDICT - an FP7-funded project enabling personalised medicine for patients with metastatic colorectal cancer.
Dataset
EGAD00001008463
-
WGS of high grade serous ovarian tumours and matched blood normals
Dataset
EGAD00001010135
-
Whole exome and Transcriptome sequencing of treatment-naïve esophageal adenocarcinoma biopsies and matched peripheral blood mononuclear cells
Dataset
EGAD00001010876
-
1M-scBloodNL
Dataset
EGAD00001007764
-
Identification of the Global miR-130a Targetome Reveals a Novel Role for TBL1XR1 in Hematopoietic Stem Cell Self-Renewal and t(8;21) AML
Dataset
EGAD00001008412
-
Genomics of Malignant Peripheral Nerve Sheath Tumor (MPNST)
Dataset
EGAD00001008608
-
WGS of high grade serous ovarian tumours and matched blood normals
Dataset
EGAD00001009049
-
RNA sequencing data for primary and recurrent ovarian granulosa cell tumors
Dataset
EGAD00001009108
-
Somatic mutation and selection at epidemiological scale - TwinsUK_TargetedNanoSeq_Buccal
Dataset
EGAD00001015618