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Data Access Commitee for Dietrich and Wendisch et al., SARS-CoV-2 infection triggers profibrotic macrophage responses and lung fibrosis (Submitted)
Dac
EGAC00001001884
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Data Access Commitee for Dietrich and Wendisch et al., SARS-CoV-2 infection triggers profibrotic macrophage responses and lung fibrosis (Submitted)
Dac
EGAC00001002335
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MethylationEPIC_JMML_tech_Schoenung
Dataset
EGAD00010001998
-
MethylationEPIC_JMML_valid_Schoenung
Dataset
EGAD00010002000
-
Methylation450k_JMML_meta_Schoenung
Dataset
EGAD00010001999
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Genome-wide array data from Eivissa and Menorca
Dac
EGAC50000000297
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Genetic investigation of 12q-amplified osteosarcomas
Dac
EGAC50000000340
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Genome-wide association study of esophageal squamous cell cancer identifies shared and distinct risk variants in African and Chinese populations
Study
EGAS00001007477
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AngioPredict CNV and Exome data
Dataset
EGAD00001004031
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H3K4me3, IgG, and Input ChIP-seq in overexpression of pLV Control, CS-FL and CS-ΔEx4 in SW1116 cells.
Study
EGAS00001008121
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Single Cell Analysis of Healthy and Diseased Temporomandibular Joint Synovial Fluid
Study
phs003645
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Whole genome sequencing of pheochromocytoma and paraganglioma arising from germline SDHB mutations
Dataset
EGAD50000000502
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Analysis of genes associated with autistic spectrum disorder, schizophrenia, and bipolar disorder.
Study
JGAS000731
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Transcriptome analysis of iPSC-derived hepatocytes from Wilson's Disease patients and healthy controls
Study
JGAS000382
-
Demographic History and Local Adaptation in Asian Population
Study
JGAS000238
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Five Mantle Cell Lymphoma Patients Before and After Failure of Standard Chemotherapy
Dataset
EGAD50000001213
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We evaluate the PGD/PGS including 129 couples with NGS test and 266 couples with SNP-array test for the detection of embryonic chromosomal abnormalities.
Study
EGAS00001000981
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Analysis of tumor periphery and center-specific mutations in renal cell carcinoma
Study
EGAS00001001784
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Detecting and tracking circulating tumour DNA copy number profiles during first line chemotherapy in oesophagogastric adenocarcinoma
Study
EGAS00001003695
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Whole genome sequencing of tumour and matched normal from patients with family history of breast cancer
Study
EGAS00001003305
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Whole-exome variant calling of individuals from the study of sepsis and acute distress respiratory syndrome in Spain
Study
EGAS50000001119
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Cell line data (RNAseq, ATACseq, ChIPseq)
Dataset
EGAD00001005493
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Berlin Neuroblastoma Patient Genomic Data from Targeted Sequencing for Detection of TERT rearrangement breakpoints to monitor neuroblastoma
Dataset
EGAD00001011088
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Paired RNA-Seq of fCAB treated and bisulfite treated VDH01, partly depleted for NSUN3
Dataset
EGAD00001008742
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NLG-LBC-05 ctDNA project sequencing data
Dataset
EGAD00001009337
-
Whole exome and RNA sequencing data from urothelial bladder cancer patients treated with anti-PD-(L)1
Dataset
EGAD00001010324
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WTS data of patients diagnosed with NKTL
Dataset
EGAD00001005230
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Pilot experiment on functional genomics in osteoarthritis_RNA
Dataset
EGAD00001001331
-
National Eye Institute (NEI) Age-Related Eye Disease Study (AREDS)
Study
phs000001
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Analysis of Donor Pancreata Defines the Transcriptomic Signature and Microenvironment of Early Neoplastic Pancreatic Lesions
Study
phs003229
-
Genetic Neuroscience: How Human Genes and Alleles Shape Neuronal Phenotypes
Study
phs002032
-
Impact of Genetic Variation on Response to GO Therapy in COG-AML Trials AAML03P1 and AAML0531
Study
phs003490
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - WXS
Study
EGAS00001003275
-
The application of RNA sequencing for the diagnosis and genomic classification of pediatric acute lymphoblastic leukemia
Study
EGAS00001004212
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Ultra-Fast Patient-Derived Xenografts Identify Functional and Spatial Tumour Heterogeneities that Drive Therapeutic Resistance
Study
EGAS00001002627
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'Targeted High Throughput Sequencing in Clinical Cancer Settings: Formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity'
Study
EGAS00001000136
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - RNA-seq
Study
EGAS00001003274
-
Plasma DNA aberrations in systemic lupus erythematosus revealed by genomic and methylomic sequencing
Study
EGAS00001000962
-
Survival Benefit and Genetic Profile of Pemetrexed as Initial Chemotherapy in Selected Chinese Patients with Advanced Lung Adenocarcinoma
Study
EGAS00001004546
-
Accurate detection and classification of pediatric sarcomas based on cell-free DNA fragmentation patterns
Study
EGAS00001005127
-
Genetics and therapeutic responses to TIL therapy of pancreatic cancer PDX models
Study
EGAS00001005596
-
Germline variants in patients with rare cancers and their implications for precision cancer medicine: experiences from the Multicenter MASTER Trial by the German Cancer Consortium (HIPO_021)
Study
EGAS00001005537
-
A study of the genetic basis of evation by Acute Myeloid Leukaemia of Graft vs Leukaemia effects after allogeneic bone marrow transplantation
Dataset
EGAD00001000404
-
Tubulointerstitial fibrosis is the histological hallmark of chronic kidney disease (CKD). Hypoxia and inflammation (i.e., interleukin (IL)-1β signalling) are independent mediators of tubulointerstitial fibrosis. However, the physiological response of human kidney tubular cells to IL-1β/IL-1RI signalling under the hypoxic conditions of CKD is poorly understood and remains a clinical imperative for therapeutic targeting. This study reports that hypoxia and IL-1β act in synergy to trigger cell cycle arrest/cellular senescence of ex vivo patient-derived primary proximal tubular epithelial cells (PTECs).
Study
EGAS00001007904
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Leveraging Extended Families for Cardiovascular Disease Genomic Discovery
Study
phs002464
-
Breakpoint detection using long insert whole genome sequencing
Study
phs000646
-
NHLBI TOPMed: Genetic Epidemiology Network of Salt Sensitivity (GenSalt)
Study
phs001217
-
Genome Wide Association Study of Subjects with Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS)
Study
phs001015
-
Genomic Translation for ALS Care (GTAC) - WGS
Study
phs002973
-
Genomic Analysis of Bevacizumab-induced Hypertension
Study
phs001597
-
A Genome-Wide Association Study for Post-bronchodilator Lung Function in Children with Asthma
Study
phs001216
-
Phenotypic Signatures of Circulating Neoantigen-Reactive CD8+ T Cells in Patients with Metastatic Cancers
Study
phs003064
-
NHLBI TOPMed: Women's Health Initiative (WHI)
Study
phs001237
-
Paired Biopsy Project: West Coast Dream Team
Study
EGAS50000000327
-
Development of targeted DNA sequencing panel for brain tumors
Study
EGAS50000000699
-
scRNA-seq of human follicular lymphoma and lymph node
Dataset
EGAD50000001143
-
Papua New Guinean Lowlanders Dataset
Study
EGAS50000000033
-
Whole Exome Sequencing of Human Gastro-esophageal Cancer PDXs
Study
EGAS50000000966
-
Analysis of TKI resistant mechanism for gastrointstinal stromal tumor
Study
JGAS000039
-
Whole-genome sequencing analysis for understanding of the stepwise progression of lung adenocarcinoma
Study
JGAS000570
-
PanCancer genome analysis in 5143 Japanese cancer patients
Study
JGAS000274
-
Gene expression data of 2D duodenum organoids with or without continuous flow
Study
JGAS000256
-
WES of Mino-VEN-R Mantle Cell Lymphoma Cells
Study
EGAS50000001088
-
Prime-seq of human term placenta-derived trophoblast organoids
Study
EGAS50000000833
-
Optimized large-scale longitudinal biorepository of gastroesophageal adenocarcinoma patient-derived organoids
Study
EGAS50000001614
-
Single-nucleus RNA-seq of human fetal liver hematopoiesis
Study
EGAS50000001631
-
Single-nucleus ATAC-seq of human fetal liver hematopoiesis
Study
EGAS50000001632
-
PROMETEO
Study
EGAS50000001499
-
Transcriptional effect of 4HTBZ on Caco-2 cells
Study
EGAS50000001237
-
Chromatin activation profiling of stereotyped chronic lymphocytic leukemias reveals a subset #8 specific signature
Study
EGAS00001006457
-
Pharmacogenomic profiling reveals molecular features of chemotherapy resistance in IDH wild type primary glioblastoma
Study
EGAS00001006989
-
Acute_Lymphoblastic_Leukemia_Exome_sequencing_2_
Study
EGAS00001000200
-
Immuno-genomic landscape of osteosarcoma
Study
EGAS00001004197
-
Single cell RNA-sequencing (scRNA-seq) of the human hematopoietic stem cell compartment (CD34+CD38-CD45RA-)
Study
EGAS00001004769
-
Whole genome sequencing of colon organoid cultures with artificially induced oncogenic mutations
Study
EGAS00001001969
-
Germline alterations of acute myeloid leukemia
Study
EGAS00001002760
-
Precursor_lesions__clonal_architecture_and_relapse_in_Wilms_nephroblastoma
Study
EGAS00001001422
-
The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR_Custom
Study
EGAS00001002257
-
Acute_Lymphoblastic_Leukemia_Exome_sequencing
Study
EGAS00001000201
-
Myeloproliferative_Disorder_Sequencing
Study
EGAS00001000198
-
Exome_sequencing_of_Congenital_Heart_Disease_families_Royal_Brompton
Study
EGAS00001000187
-
Myeloproliferative_Disorder_Sequencing
Study
EGAS00001000199
-
DNA Methylation-based diagnostic biomarkers for ESCC in Han Chinese population
Study
EGAS00001003158
-
Epigenetics/genetics of the patient-derived xenografts of pediatric T-cell leukemia
Study
EGAS00001003248
-
Acute_Lymphoblastic_Leukemia_Sequencing
Study
EGAS00001000058
-
The NIHR BioResource Rare Diseases BRIDGE consortium sequencing projects
Study
EGAS00001001012
-
Genome-wide search to find the genetic elements underlying visual contour perception
Study
EGAS00001003639
-
FinHer_Breast_Cancer_Study
Study
EGAS00001000648
-
Genomic Landscape of Pediatric Myelodysplastic Syndromes
Study
EGAS00001002202
-
KIR gene content imputation from single-nucleotide polymorphisms in the Finnish population
Study
EGAS00001005457
-
Gene expression profiling of nasopharyngeal carcinoma
Study
EGAS00001004542
-
A transcriptome atlas of human skeletal muscles
Study
EGAS00001005904
-
CUT&RUN of AML1-ETO binding occupancy following miR-130a KD in Kasumi-1 cells
Study
EGAS00001005867
-
Gene_regulation_of_human_CD4__Treg_cells_
Study
EGAS00001003516
-
Placebo-only arm transcriptomic analysis of the phase 3 PROTECT clinical trial
Study
EGAS00001006344
-
Immuno-genomic landscape of osteosarcoma
Study
EGAS00001003887
-
Diagnosis of multisystem inflammatory syndrome in children by a whole-blood transcriptional signature
Study
EGAS00001007409
-
FASTQ files of the polyA+ (oligo-dT) RNA-Seq dataset from the POPS SGA (Small for Gestational Age) samples and their matched controls.
Dataset
EGAD00001006304
-
WES, sWGS and RNA-seq of Asian breast cancer
Dataset
EGAD00001006399
-
A developmental cell atlas of the human thyroid gland - WGS
Dataset
EGAD00001015447