-
Spatial transcriptomics analysis of HPV-dependent and HPV-independent vulval squamous cell carcinoma
Study
EGAS00001007981
-
Amplicon sequencing of various tumors
Study
JGAS000366
-
CRC Promoter capture Hi-C
Study
EGAS00001001946
-
PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysm in humans
Study
EGAS00001005518
-
Single cell sequencing data of PBMC and CSF from a cohort of Multiple Sclerosis patients and other neurological disease controls
Study
EGAS50000000739
-
Genetic Basis of Hepatosplenic T Cell Lymphoma (HSTL)
Study
EGAS00001002182
-
Phase 1 CX-5461 Trial (Canadian Cancer Trials Group Trial IND.231)
Study
EGAS00001006173
-
Exome & MiSeq sequencing of individuals with Huntington's disease
Study
EGAS00001006383
-
Serial TERT rearrangement breakpoint quantification in circulating tumor DNA enables minimal residual disease monitoring in patients with neuroblastoma
Study
EGAS00001007365
-
Unraveling mutagenic processes influencing the tumor mutational patterns of individuals with Constitutional Mismatch Repair Deficiency
Study
EGAS00001007660
-
Cholesterol homeostasis and lipid raft dynamics at the basis of tumor-induced immune dysfunction in chronic lymphocytic leukemia
Study
EGAS50000000933
-
Biased allelic expression in human primary fibroblast single cells.
Study
EGAS00001001009
-
Transcriptomic characterization of the histopathological growth patterns in breast cancer liver metastases
Study
EGAS50000000225
-
Integrative Analysis of Lung Adenocarcinoma in EAGLE (Version 2)
Study
phs001169
-
Volasertib preclinical activity in high-risk hepatoblastoma
Study
EGAS00001004827
-
Linguistic utterance counts for The admixture histories of Cabo Verde
Dataset
EGAD00001008978
-
Whole genome sequencing of matched primary and metastatic acral melanomas
Study
EGAS00001000169
-
Knoll et al.: The life-saving benefit of dexamethasone in severe COVID-19 is linked to a reversal of monocyte dysregulation
Study
EGAS00001007461
-
Inhibiting DNA Methylation Causes an Interferon Response in Cancer via dsRNA Including Endogenous Retroviruses
Study
phs001038
-
The landscape of somatic mutations in epigenetic regulators across 1000 pediatric cancer genomes
Study
EGAS00001000449
-
Lung Health Study (LHS-BioLINCC)
Study
phs004013
-
Sensitive and robust liquid biopsy-based detection of PIK3CA mutations
Study
EGAS00001004940
-
Methylation differences in trisomy 21 using monozygotic twins
Study
EGAS00001001051
-
Structure and evolution of double minutes in diagnosis and relapse brain tumors
Study
EGAS00001003212
-
54 metastatic colorectal cancer patients from Schleswig-Holstein in North Germany
Study
EGAS00001004108
-
ATAC-seq data in normal colon mucosa
Study
EGAS00001005281
-
Frequent mutation of the FOXA1 untranslated region in prostate cancer
Study
EGAS00001003113
-
RNA-Seq of GM adipose tissue samples
Dataset
EGAD00001010253
-
Systematic analysis of paralogous regions in 41,755 exomes uncovers clinically relevant variation
Study
EGAS00001007513
-
Genomic analysis of primary plasma cell leukemia reveals complex structural alterations and high risk mutational patterns
Study
phs002022
-
Xeroderma Pigmentosum, Complementation Group C, (XPC) and Non-XPC Cutaneous Squamous Cell Carcinoma (cSCC) Mutation Rate Study
Study
phs000830
-
Novel mutations in TOP2A in gliomas
Study
EGAS00001004556
-
Kids First: Genomics of Orofacial Clefts in the Philippines
Study
phs002595
-
Altered enhancer-promoter interaction leads to MNX1 expression in pediatric acute myeloid leukemia with t(7;12)(q36;p13)
Study
EGAS50000000130
-
RTEL1 mutation as a modifier of Dyskeratosis Congenita in a family with a Telomerase RNA (hTR) template mutation and variant telomeric repeats
Study
EGAS50000001644
-
BLUEPRINT DNA methylation profiles of graft donors in allogenic hematopoietic stem cell transplantation
Study
EGAS00001001287
-
Combined Metabolic Activators Reduces Liver Fat in Nonalcoholic Fatty Liver Disease Patients
Study
EGAS00001005616
-
Epigenomic analysis of the human placenta and endometrium constituting the fetal-maternal interface
Study
JGAS000073
-
Epigenomic analysis of the human placenta and endometrium constituting the fetal-maternal interface
Study
JGAS000107
-
Changes in CRISPR/Cas9 Outcomes depending on the usage of Pifithrin-alpha
Study
EGAS50000000656
-
BS-seq in plasma of CRC patients
Study
EGAS00001003117
-
Genomic Sequencing of Cervical Cancers
Study
phs000600
-
CRISPR/Cas9-mediated genome editing of Schistosoma mansoni acetylcholinesterase
Study
EGAS00001004455
-
The KATHERINE study of adjuvant trastuzumab emtansine in HER2-positive breast cancer: analysis of patients with HER2-negative residual invasive disease on re-testing
Study
EGAS00001006037
-
Whole exome sequencing in RVOT patients
Study
EGAS00001002319
-
Germline variants collaborate with somatic mutations and initiate and/or drive disease in primary myelodysplastic syndrome (MDS) and therapy-related myeloid neoplasms (t-MN)
Study
EGAS00001003547
-
Efficacy of JAK/STAT pathway inhibition in murine xenograft models of early T-cell precursor (ETP) acute lymphoblastic leukemia
Study
EGAS00001001146
-
Targets of MEK inhibition in DIPG
Study
EGAS00001004495
-
Single-cell Transcriptome Profiling of Treatment-naïve and Post-treatment Colorectal Cancer: Insights into Putative Mechanisms of Chemoresistance
Study
EGAS50000000830
-
Paediatric Hepatic International Tumour Trial (JPLT2: PHITT)
Study
JGAS000236
-
The_evolution_of_CML
Study
EGAS00001005095
-
Host genetic determinants of HIV infection
Study
EGAS00001005245
-
Whole-Exome Sequences from Imazighen and non-Imazghen from Tunisia
Study
EGAS00001005205
-
ctDNA quantification in Ewing sarcoma patients
Study
EGAS00001006433
-
NIDDK IBD Genetics Consortium Ulcerative Colitis Genome-Wide Association Study
Study
phs000345
-
RNA-seq of DF149 cells – a patient-derived xenograft model of ascites-derived, homologous recombination repair-proficient, high-grade serous ovarian carcinoma – cultured in vitro and isolated after 8 hours treatment with DMSO control (3 x biological replicates) and 2.5 µM CBL0137 (3 x biological replicates)
Study
EGAS00001006662
-
Shared disease specific B cell clones in Crohn’s disease
Study
EGAS50000000912
-
The Study of Somatic LINE1 Activity in Cancers
Study
phs003888
-
Molecular analysis of circulating tumour cells identifies distinct profiles in chemosensitive and chemorefractory patients with small cell lung cancer
Study
EGAS00001001951
-
Genome-wide association study of cervical cancer in East Asian populations
Study
EGAS00001003199
-
Mitochondrial DNA sequencing in samples of Huntington’s disease patients
Study
EGAS00001004092
-
Genetics causes of male infertility in 185 patient-parent trios from Netherlands and UK
Study
EGAS00001005417
-
Selection of somatic escape variants in SERPINA1 in liver tissue of patients with alpha-1 anti-trypsin deficiency - WGS
Dataset
EGAD00001015430
-
Selection of somatic escape variants in SERPINA1 in liver tissue of patients with alpha-1 anti-trypsin deficiency - Exome
Dataset
EGAD00001015431
-
Germline variants in UHRF1 are associated with multi-locus imprinting disturbance in humans and mice
Study
EGAS50000001179
-
Mutational_landscape_in_haemochromatosis__WGS_
Study
EGAS00001005157
-
Mutational_landscape_in_haemochromatosis__exome_
Study
EGAS00001005158
-
Immunomodulatory effects and improved outcomes with cisplatin- vs carboplatin-based chemotherapy plus atezolizumab in urothelial cancer
Study
EGAS50000000104
-
Intervention with Micronutrients and Long-Term Impact in Brazil-RECODISA
Study
phs003174
-
Somatic Mutations and Cell Lineage in the Human Brain
Study
phs001485
-
Integrative Age-Related Changes in Genome and Epigenome in Human Lung in Relation to Smoking
Study
phs003317
-
A Translational, Pharmacodynamic and Pharmacokinetic Phase IB Clinical Study of Everolimus in Resectable Non-Small Cell Lung Cancer
Study
phs000829
-
Hofer et al., A specific subpopulation of cancer-associated fibroblasts promotes resistance to chemotherapy in triple-negative breast cancer by upregulating G0S2 protein
Study
EGAS50000000886
-
Assessment of cannabidiol and Δ9-tetrahydrocannabiol in mouse models of medulloblastoma
Study
EGAS00001004963
-
Inactivation of TGFβ receptors in stem cells drives cutaneous squamous cell carcinoma - 30 whole exomes
Study
EGAS00001001892
-
Novel mutational mechanisms and drivers in Pancreatic Neuroendocrine Tumours
Study
EGAS00001001732
-
CTCF/cohesin-binding sites are frequently mutated in cancer
Study
EGAS00001003010
-
MGMT genomic rearrangements contribute to chemotherapy resistance in gliomas
Study
EGAS00001004544
-
Homologous recombination DNA repair deficiency and PARP inhibition activity in primary triple negative breast cancer
Study
EGAS00001004405
-
Genomics of Circulating Tumor Cells
Study
phs000717
-
Development of a diagnostic gene panel for Gorlin syndrome and its application to liquid biopsy
Study
JGAS000308
-
Using Exome-sequencing to characterize the resistance to lirafugratinib
Study
EGAS50000001371
-
Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
-
Deep multi-region whole-genome sequencing reveals heterogeneity and gene-by-environment interactions in treatment-naive, metastatic lung cancer
Study
EGAS00001003830
-
Ultrasensitive detection of minor allele fractions in maternal samples based on microhaplotype analysis
Study
EGAS00001007057
-
Comprehensive investigation of genome architecture of papillary thyroid cancer with whole-exon sequencing in the Chinese population.
Study
EGAS00001002402
-
TP53 variant detection analysis in high grade serous epithelial ovarian cancer
Study
EGAS00001004361
-
DNA-methylation variability in normal mucosa of patients with adenomatous polyps: a marker of field cancerization
Study
EGAS00001007666
-
Investigation of MMBIR DNA Repair in Normal and Cancer Human Cells
Study
phs002237
-
Temporal Dissection of Tumorigenesis in Primary Cancers
Study
phs000418
-
Whole Exome Sequencing Analysis of Carfilzomib-Related Cardiotoxicity in Multiple Myeloma Patients
Study
phs003308
-
Targeted_sequencing_of_in_vitro_colonies___bulks
Study
EGAS00001003175
-
HCA_Immune_UAI_Paediatric_Spatial_Managed_Access
Study
EGAS00001006471
-
Single cell RNA sequencing of peripheral blood HSPC from patients with sickle cell anemia and healthy donors
Study
EGAS50000001046
-
scRNA-seq of a 3D human cortical tissue model from human iPSCs exploring WT versus APP KI genotypes as well as Abeta/Aducanumab treatments
Study
EGAS50000001397
-
Targeted sequencing of brain expressed miRNA genes
Study
EGAS00001001607
-
The Jerusalem Perinatal Study (JPS) aimed to examine the developmental origins of cardiometabolic risk.
Study
EGAS00001004075
-
Blood RNA-seq from Mexican DMD patients and healthy controls
Study
EGAS00001004907
-
Transcriptome Analysis of Malignant Peripheral Nerve Sheath Tumor-like Melanoma
Dataset
EGAD00001007000
-
DNA Methylation Analysis of Prostate Cancer Cell Lines and Tissues Using Next Generation Sequencing
Study
phs000597