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Tumor inflammation and mutational burden are differentially associated with response to nivolumab or nivolumab plus ipilimumab in metastatic colorectal cancer
Study
EGAS50000000416
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Maturation of Human Intestinal Epithelial Cell Layers Fortifies the Apical Surface against Salmonella Attack
Study
EGAS50000001241
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WGS analysis of Japanese liver cancer
Study
JGAS000151
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Parent-of-origin dependent DNA methylation and gene expression in the human placenta
Study
JGAS000038
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A tumor-associated photoreceptor signature unifies distinct central nervous system malignancies
Study
EGAS50000001457
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Single Cell RNA Transcriptomics of Mantle Cell Lymphoma Reveals the Presence of Treatment-Resistant Subclones at the Time of Diagnosis
Study
EGAS50000000825
-
Transcriptome changes in circulating immune cells of critical COVID-19 patients predict a specific metabolic and epigenetic imprint
Study
EGAS50000000965
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STimage: Robust and interpretable prediction of gene markers and cell types from spatial transcriptomics data
Study
EGAS50000001503
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Monosomy 7 delineates a primitive acute myeloid leukemia with adverse prognosis and responsiveness to epigenetic therapy
Study
EGAS50000001641
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GEenetic landscape of hypodiploid acute lymphoblastic leukemia
Study
EGAS00001000380
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Whole genome sequencing data for 10 hepatocellular carcinomas (HCC) and matched non-tumor liver tissues + optical mapping data for 4 HCC and 3 matched non-tumor liver tissues.
Study
EGAS00001005629
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Human induced pluripotent stem cells display a similar mutation burden as embryonic pluripotent cells in vivo
Study
EGAS00001005939
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Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
Study
EGAS00001000443
-
Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
-
Single-cell RNA-seq of cervix and placenta
Study
EGAS00001007044
-
A Genomic History of Aboriginal Australia
Study
EGAS00001001766
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Early evolutionary branching across spatial domains predisposes to clonal replacement under chemotherapy in neuroblastoma
Study
EGAS00001007650
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Myelodysplastic cells in patients re-program mesenchymal stromal cells to establish a transplantable stem cell-niche disease unit.
Study
EGAS00001000716
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Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
Study
EGAS00001000941
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Comparing nodal versus bony metastatic spread using tumour phylogenies
Study
EGAS00001001801
-
Whole_genome_sequencing_in_a_multiplex_Crohn_s_disease_family
Study
EGAS00001000060
-
Impact of mutational profiles on response of primary oestrogen receptor-positive breast cancers to oestrogen deprivation
Study
EGAS00001001940
-
Genetic Basis of Hepatosplenic T Cell Lymphoma (HSTL)
Study
EGAS00001002182
-
EATL-II STUDY
Study
EGAS00001001879
-
Inactivation of TGFβ receptors in stem cells drives cutaneous squamous cell carcinoma - 30 whole exomes
Study
EGAS00001001892
-
Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas
Study
EGAS00001001916
-
Orthotopic Patient-Derived Xenografts of Pediatric Solid Tumors
Study
EGAS00001002528
-
Transcriptome analysis in very preterm infants with chronic lung disease after birth
Study
EGAS00001002586
-
Whole-exome ultra-high throughput sequencing in brain samples of suicide victims who had suffered from major depressive disorder and control subjects who had died from other causes
Study
EGAS00001002818
-
Spatial genomic heterogeneity in multiple myeloma revealed by multi- region sequencing
Study
EGAS00001002111
-
MGA-NUTM1 fusion in high grade spindle cell sarcoma
Study
EGAS00001003341
-
miR-200-regulated CXCL12β promotes fibroblast heterogeneity and immunosuppression in ovarian cancers
Study
EGAS00001002184
-
Clinical Implications of Genomic Alterations in the Tumor and Circulation of Pancreatic Cancer Patients
Study
EGAS00001001257
-
Epigenomics and Single-cell Sequencing Define a Developmental Hierarchy in Langerhans Cell Histiocytosis
Study
EGAS00001003822
-
SG10K_Pilot - Large-scale whole-genome sequencing of three diverse Asian populations in Singapore
Study
EGAS00001003875
-
DONSON encodes a novel replication fork protection factor mutated in microcephalic dwarfism.
Study
EGAS00001002224
-
HCA_Gonads_Foetal_EU_H2020_HUGODECA_RNA
Study
EGAS00001004723
-
Rna-Seq Leiomyosarcoma subtypes
Study
EGAS00001004783
-
Divergence between high metastatic tumor burden and low circulating tumor DNA concentration in metastasized breast cancer
Study
EGAS00001000625
-
Data from the paper Context-specific Effects of TGFβ/SMAD3 in Cancer Are Modulated by the Epigenome. Tufegdzic et al, Cell Reports 2015
Study
EGAS00001001570
-
Tracking the genomic evolution of esophageal adenocarcinoma through neoadjuvant chemotherapy
Study
EGAS00001001254
-
Integrative genomic and transcriptomic analysis of adult leiomyosarcoma (HIPO-028, HIPO-018, HIPO-021)
Study
EGAS00001002437
-
Novel mutational mechanisms and drivers in Pancreatic Neuroendocrine Tumours
Study
EGAS00001001732
-
A biobank of patient-derived pediatric brain tumor models
Study
EGAS00001002536
-
The genomic landscape of cutaneous squamous cell carcinoma from immunosuppressed and immunocompetent patients reveals common drivers and a novel mutational signature associated with chronic azathioprine exposure
Study
EGAS00001002612
-
Dynamics of neoantigen landscape during immunotherapy
Study
EGAS00001002704
-
Exome Sequencing of Gastric Cancer
Study
EGAS00001000153
-
Exome_sequencing_of_blastic_plasmacytoid_dendritic_cell_neoplasms
Study
EGAS00001000171
-
Whole Exome sequencing of Gingivo-buccal Cancer : ICGC-India Project_Batch04
Study
EGAS00001002852
-
The interface of malignant and immunologic clonal dynamics in high-grade serous ovarian cancer
Study
EGAS00001002839