-
The T cell receptor repertoire of tumor infiltrating T cells is predictive and prognostic for cancer survival
Study
EGAS00001005201
-
High-grade serous ovarian cancer refined with single-cell RNA-sequencing
Study
EGAS00001004987
-
Dissecting the Spatial Heterogeneity of Single Circulating Tumor Cells in Hepatocellular Carcinoma
Study
EGAS00001005204
-
RNA sequencing data of 66 matched primary and recurrent high grade serous ovarian cancer
Study
EGAS00001002660
-
The_British_Autozygosity_Populations_BioResource
Study
EGAS00001002742
-
Comprehensive molecular profiling of high-grade serous ovarian cancer
Study
EGAS00001003804
-
Solve-RD Solving the Unsolved Rare Dieseases
Study
EGAS00001003851
-
Platelet response in aspirin adherent pregnant women
Study
EGAS00001005188
-
Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples
Study
EGAS00001005323
-
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___BD___WGS
Study
EGAS00001003014
-
The WID-CIN test identifies women with, and at risk of, cervical intraepithelial neoplasia grade 3 and invasive cervical cancer (CIN3+)
Study
EGAS00001005078
-
COVID_19_Challenge_Project_Single_Cell_Profiling
Study
EGAS00001005696
-
Whole genome sequencing of multiple myeloma identifies novel structural and non-coding mutations.
Study
EGAS00001003164
-
The distinct DNA methylome of acute lymphoblastic leukemia
Study
EGAS00001005203
-
Sequencing of an adolescent patient with germline RET mutant alveolar rhabdomyosarcoma
Study
EGAS00001004359
-
Genomic characterization of co-existing biliary tract intraepithelial neoplasia and carcinoma lesions reveals distinct evolutionary paths of gallbladder cancer
Study
EGAS00001005402
-
Identifying the role of ID3 in DNA repair and maintenance of genome integrity
Study
EGAS00001004478
-
Acquiring and sequencing of all 24 single human chromosomes
Study
EGAS00001003300
-
Genomewide copy number alteration screening of circulating plasma DNA
Study
EGAS00001006031
-
USARC 10X Genomics Single Cell DNA Sequencing Data
Study
EGAS00001006144
-
scRNAseq of human primary nasal epithelium differentiated at air-liquid interface exposed to SARS-CoV2
Study
EGAS00001005633
-
DGCR8 and the six hit, three-step model of schwannomatosis
Study
EGAS00001005665
-
Cell-free DNA and bone marrow samples from myelodysplastic syndromes
Study
EGAS00001005992
-
Induced pluripotent stem cell lines (iPSC lines) produced from skin and blood cells.
Study
EGAS00001006262
-
Single cell multi-omic data of glioblastoma evolution under therapy
Study
EGAS00001004909
-
Deep whole genome sequencing identifies recurrent genomic alterations in breast cancer cell lines and patient derived xenograft models
Study
EGAS00001006285
-
Endothelium-derived stromal cells contribute to bone marrow niche formation
Study
EGAS00001004946
-
Characterization of MCSP+ melanoma DCC and MelDCC lines
Study
EGAS00001006702
-
Tumorigenic role of Musashi-2 in aggressive mantle cell lymphoma
Study
EGAS00001006613
-
Single cell RNAseq of lung adenocarcinoma
Study
EGAS00001005021
-
Clonal dynamics of normal hepatocyte expansions in homeostatic human livers and their association with the biliary epithelium
Study
EGAS00001006962
-
Molecular analysis of cancer genomes in children with Lynch syndrome: exploring causal associations
Study
EGAS00001007146
-
Cachexia - Non-Cachexia Metagenome Analysis
Study
EGAS00001007156
-
Multiomic profiling of pleomorphic rhabdomyosarcoma
Study
EGAS00001007230
-
Idiosyncratic and generic single nuclei and spatial transcriptional patterns in papillary and anaplastic thyroid cancers
Study
EGAS00001007574
-
Lung_Cell_Atlas__Paediatric_RNA
Study
EGAS00001008299
-
Transcriptomic predictors of survival for palbociclib + endocrine therapy vs. capecitabine in aromatase inhibitor-resistant breast cancer from GEICAM/2013-02 PEARL
Study
EGAS00001008177
-
Lung_Cell_Atlas__Paediatric_Spatial
Study
EGAS00001008300
-
Multiregional single nuclei RNA-seq and WGS of prostate cancer
Dataset
EGAD50000001357
-
Variant calling dataset from the whole-exome study of familial pulmonary fibrosis in the Canary Islands-VCF files
Dataset
EGAD50000001152
-
fragmentomic features of individuals with different cfDNA concentrations
Dataset
EGAD50000000970
-
RNA sequencing from patient-derived intestinal organoids
Dataset
EGAD50000000492
-
GSA QCed data
Dataset
EGAD00010002568
-
EGAD00010000630
Dataset
EGAD00010000630
-
Genome and transcriptome sequence data from a metastatic cholangiocarcinoma patient
Dataset
EGAD00001002976
-
Genome and transcriptome sequence data from a breast cancer patient
Dataset
EGAD00001002972
-
Genome and transcriptome sequence data from a rectal adenocarcinoma patient
Dataset
EGAD00001002973
-
Genome and transcriptome sequence data from a cholangiocarcinoma patient
Dataset
EGAD00001002991
-
Genome and transcriptome sequence data from a leiomyosarcoma patient
Dataset
EGAD00001002996
-
Genetics of gene expression in human macrophage response to Salmonella
Dataset
EGAD00001003204
-
Whole exome and targeted DNA sequencing data for formalin-fixed paraffin embedded tissue from de novo small cell prostatic carcinoma cases
Dataset
EGAD00001004139
-
Exome sequencing of 142 gastric cancer and matched normal from Japanese cohorts (UT)
Dataset
EGAD00001004041
-
Exome sequencing of 102 gastric cancer and matched normal from Japanese cohorts (YCU)
Dataset
EGAD00001004042
-
WGBS data of solid liver tumor DNA, and WGBS data of cell-free DNA derived from human blood, for CancerDetector study
Dataset
EGAD00001004317
-
Whole Exome DNA Sequencing of matched brain tumor-normal pairs
Dataset
EGAD00001000698
-
Anaplastic Meningioma WGS-X10
Dataset
EGAD00001001267
-
Functional genomics approaches to understand osteoarthritis (2019-08-01)
Dataset
EGAD00001005215
-
Profiling molecular heterogeneity in human primary microglia
Dataset
EGAD00001005736
-
Pseudotime ordering of cell cycle state (2020-01-29)
Dataset
EGAD00001005919
-
Transcriptome Analysis of Malignant Peripheral Nerve Sheath Tumor-like Melanoma
Dataset
EGAD00001007000
-
Combinatorial CRISPR screen identifies fitness effects of paralogues FAM50A and FAM50B
Dataset
EGAD00001006649
-
Rare Disease Synthetic Dataset
Dataset
EGAD00001008392
-
Blood neutrophils in COPD derive from activated progenitors in the bone marrow
Dataset
EGAD00001008788
-
Blood neutrophils in COPD derive from activated progenitors in the bone marrow sc Seqwell
Dataset
EGAD00001008908
-
Blood neutrophils in COPD derive from activated progenitors in the bone marrow sc Rhapsody
Dataset
EGAD00001009704
-
scEC&T-seq manuscript data
Dataset
EGAD00001010071
-
Tumour evolvability metrics predict recurrence in advanced localised prostate cancer (normal data)
Dataset
EGAD00001010295
-
Tumour evolvability metrics predict recurrence in advanced localised prostate cancer (tumour data)
Dataset
EGAD00001010274
-
Organoid Derivation Project - GRCh38 - WGS (2023-06-22)
Dataset
EGAD00001011093
-
NOTCH1 fusion genes in pediatric T-cell lymphoblastic lymphoma hallmark a common high-risk subgroup with blood TARC levels as possible biomarker
Dataset
EGAD00001015255
-
Genomic and transcriptomic landscape of T-cell lymphoblastic lymphoma compared to T-cell acute lymphoblastic leukemia: similar subtypes and different fusions
Dataset
EGAD00001015357
-
The G2 gene expression signature and MYC overexpression are independent poor prognostic factors in childhood high-grade osteosarcoma
Dataset
EGAD00001015502
-
Bulk RNAseq gene expression of baseline tumors from metastatic urothelial bladder cancer patients (IMvigor210) and metastatic renal cell carcinoma (IMmotion150)
Study
EGAS00001004386
-
Whole genome sequencing of primary and metastatic Melanoma cases in an Australian cohort.
Study
EGAS00001001552
-
Adipose transcriptome response after a 6-day very-low energy fast in obesity, in the single-arm feeding trial FASTOMICS-6
Dataset
EGAD50000001484
-
Convergent evolution drives therapy resistance in DNA repair-deficient mCRPC
Study
EGAS00001007147
-
Comprehensive Genomic Profiling of a National Cohort of Pediatric Papillary Thyroid Carcinoma in Hungary
Study
EGAS50000001833
-
Metabolomic and microbiome profiling reveals personalized risk factors for coronary artery disease
Study
EGAS00001005342
-
H3Africa - Consortium WGS
Study
EGAS00001005972
-
PCR-free HiSeqX whole genome sequence data on 120 samples with triplet repeat expansions (premutation and full expansions)
Study
EGAS00001002462
-
Disorders/Differences of Sex Development (DSD) Study Performed at UCLA in Collaboration with the DSD-Translational Research Network (DSD-TRN), with the Support of the Gabriella Miller Kids First Pediatric Research Program
Study
phs001178
-
Relationship between low LDL cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: a US-based cross-sectional observational study using electronic medical records
Study
phs001588
-
Sporadic Amyotrophic Lateral Sclerosis (ALS): Parent-Offspring and Twin Sequencing Study
Study
phs000831
-
The PEMDAC phase 2 study of pembrolizumab and entinostat in patients with metastatic uveal melanoma
Study
EGAS00001005478
-
Summary statistics from genome-wide association study in glioma of 12,488 cases and 18,169 controls.
Study
EGAS00001003372
-
RNA-seq study of human long-term and short-term hematopoietic stem cells from umblical cord blood with lentiviral overexpression of S1PR3
Study
EGAS00001004798
-
FASTQ files of total RNA-Seq data from the POPS SGA (Small for Gestational Age) samples
Dataset
EGAD00001003507
-
FASTQ files of total RNA-Seq data from the POPS PET (pre-eclamptic) samples
Dataset
EGAD00001003508
-
NIPT samples for systematic evaluation of NIPT aneuploidy detection software tools
Dataset
EGAD00001007712
-
A Tumour Organoid Biobank for Mapping Cancer Cell Vulnerabilities - WGS
Dataset
EGAD00001015469
-
Clinical outcomes and immune correlates of response to nivolumab plus chemoradiotherapy in women with locally-advanced cervical cancer – NiCOL study
Study
EGAS00001007297
-
Whole Genome Sequencing to Discover Familial Myeloma Risk Genes
Study
phs001819
-
Accurate Genome-Wide Germline DNA Profiling from Decade-Old Archival Tissue Specimens
Study
phs002865
-
Genomic Landscape of Cutaneous Diffuse Large B Cell Lymphoma
Study
phs001645
-
Organoid Profiling Identifies Common Responders to Chemotherapy in Pancreatic Cancer
Study
phs001611
-
Genomic Characterization of Meningiomas
Study
phs000552
-
Performance Characteristics of Selective Targeted Enrichment in Genetic Diagnostic Testing
Study
phs000798
-
Exome Sequencing in Schizophrenia Families
Study
phs000738
-
Transcriptome and TCR Sequencing of T Cells from Metastectomies
Study
phs002748
-
CALGB/SWOG 80405 ct DNA Biomarker Evaluation
Study
phs002941