-
Melanoma transcriptomic data from patients undergoing immunotherapy
Dataset
EGAD50000001569
-
LongVar low-coverage data
Dataset
EGAD50000001607
-
Single cell and spatial transcriptomics of adult human adrenal glands
Dataset
EGAD50000000394
-
RNA sequencing from High-grade B-cell lymphoma, not otherwise specified: an LLMPP study
Dataset
EGAD50000001365
-
Whole genome sequencing from High-grade B-cell lymphoma, not otherwise specified: an LLMPP study
Dataset
EGAD50000001366
-
circulating cell-free RNAs, CF-miRNAs, Sequencing with Qiaseq and NextSeq 550
Dataset
EGAD50000001503
-
Long-read Nanopore data EVOFLUx
Dataset
EGAD50000001697
-
Shallow Whole Genome Sequencing (sWGS) of pancreatic ductal adenocarcinoma
Dataset
EGAD50000001732
-
RNA-sequencing of PBMCs from COVID-19 patients experiencing different degrees of the disease (mild and critical), and control patients
Dataset
EGAD50000001405
-
miRNA-sequencing of PBMCs from COVID-19 patients experiencing different degrees of the disease (mild and critical), and control patients
Dataset
EGAD50000001406
-
prostate cancer plasma cfRNA
Dataset
EGAD50000001805
-
WGS data for Pancreatic Cancer samples (misc.)
Dataset
EGAD50000001833
-
Genome editing strategies to generate working models in Polycystic Kidney Disease
Dataset
EGAD50000001694
-
Targeted sequencing data on sequential liquid biopsy samples from mCRPC patients receiving cabazitaxel
Dataset
EGAD50000001840
-
Single cell multi modal dataset of bone marrow samples from follicular lymphoma patients at diagnosis et one year post treatment
Dataset
EGAD50000001843
-
p200503_fn1
Study
EGAS50000001120
-
Olink Target Protein Expression
Dataset
EGAD50000001328
-
Sequencing dataset for the Predictive Endocrine ResistanCe Index (PERCI) in Breast Cancer cases
Dataset
EGAD50000001595
-
DNA sequencing of sgRNAs enriched from the CRISPR-Cas9 screened HCC organoids
Study
EGAS50000001130
-
cfDNA sWGS BAM — NSCLC stage I–III
Dataset
EGAD50000001878
-
Exome Sequencing data from infertility cases.
Dataset
EGAD50000001881
-
Human colorectal cancer single-cell RNA sequencing
Study
EGAS50000001348
-
Pediatric B-cell precursor acute lymphoblastic leukemia Micro-C sequencing
Study
EGAS50000000764
-
Non-invasive bladder cancer cfDNA dataset
Dataset
EGAD50000001935
-
Human embryonic stem cells dopaminergic neurons scRNA-seq
Dataset
EGAD50000001592
-
Whole-exome variant calling of individuals from the study of familial pulmonary fibrosis in the Canary Islands
Study
EGAS50000000782
-
RNA-seq
Dataset
EGAD50000002023
-
ctDNA detectability and representativeness in seven body liquids from female patients with metastatic breast cancer - lpWGS
Study
EGAS50000001302
-
ctDNA detectability and representativeness in seven body liquids from female patients with metastatic breast cancer - WES
Study
EGAS50000001303
-
Bulk RNAseq dataset for "Longitudinal Multi-Omics Study Reveals Molecular Drivers and Tumor Microenvironment in Extramedullary Multiple Myeloma"
Dataset
EGAD50000000051
-
UK_exomechip
Dataset
EGAD00010002019
-
UK_immunochip
Dataset
EGAD00010002049
-
Bulk RNA sequencing of metastatic colorectal cancer patient-derived xenografts with known response to irinotecan
Dataset
EGAD50000002138
-
Single-cell transcriptomic data of 9 DHG-H3G34 patient tumors.
Study
EGAS50000000534
-
Epigenomic dataset of Human Hepatocellular Carcinoma for EpiHK
Study
EGAS50000000039
-
Clonal_analysis_Bcell_activation
Dataset
EGAD50000002114
-
Raw scRNA-seq data for “Characterization of intestinal immune responses in generalized human and murine lipodystrophy”
Dataset
EGAD50000002190
-
Raw scTCR-seq data for “Characterization of intestinal immune responses in generalized human and murine lipodystrophy”
Dataset
EGAD50000002191
-
Targeted capture sequencing data from 107 classical Hodgkin Lymphoma tumors and 25 corresponding normal samples.
Dataset
EGAD50000002163
-
Dataset of Recurrent resistance mutations to lirafugratinib delineate treatment sequences for FGFR2-driven tumors
Dataset
EGAD50000001981
-
Flexible and rapid validation of structural variants using adaptive sampling
Dac
EGAC50000000748
-
Circulating immune cell landscape in colorectal cancer patients
Study
EGAS50000000590
-
WGS of all Patients Listed within this Study
Dataset
EGAD50000002362
-
Ribo-depleted RNA-sequencing of II.3, III.1, and III.3
Dataset
EGAD50000002364
-
Unraveling the Physiological Impact of ANGPTL8 Loss-of-Function Variants in Humans
Study
EGAS50000001482
-
10X snMultiome (ATAC+GEX) sequencing of 5 human reactive tonsil samples
Dataset
EGAD50000002366
-
ChIP-seq for 10 samples
Dataset
EGAD50000001786
-
Noninvasive detection of cancer-associated genome-wide hypomethylation and copy number aberrations by plasma DNA bisulfite sequencing
Study
EGAS00001000566
-
Angiosarcoma_follow_up_study
Study
EGAS00001000405
-
Feasibility_of_targeted_capture_sequencing_in_routinely_collected_FFPE_cancer_specimens
Study
EGAS00001000297
-
BLUEPRINT DNA methylation profiles of monocytes, T cells and B cells in type 1 diabetes-discordant monozygotic twins
Study
EGAS00001001598
-
MPN_mutation_order_followup
Study
EGAS00001000663
-
Chromatin_Profiling_in_Twins
Study
EGAS00001000097
-
EBV_AID_project
Study
EGAS00001000955
-
Osteosarcoma_Whole_Genome
Study
EGAS00001000147
-
Genomic characterization of Malignant Pleural Mesothelioma.
Study
EGAS00001001563
-
Feasibility_of_targeted_capture_sequencing_in_FFPE_cancer_specimens_2
Study
EGAS00001000402
-
Analysis_of_somatic_mutations_in_normal_blood__AML_and_MDS_samples
Study
EGAS00001000525
-
Prognostic_factors_in_prostate_cancer__deep_sequencing_pilot_project_TAPG
Study
EGAS00001000879
-
FFPE_CPA_Accreditation_Study
Study
EGAS00001000466
-
Angiosarcoma_follow_up_2_validation_study
Study
EGAS00001000518
-
Ewings_Sarcoma_RNA_seq_drug_sensitivity
Study
EGAS00001000419
-
FFPE_CPA_Accreditation_Study__Part_2
Study
EGAS00001000692
-
Bone_Cancer___Rare_Types_Whole_Genome
Study
EGAS00001000501
-
LINE_luminal_breast_cancer_Neoadjuvant_Chemotherapy_Study
Study
EGAS00001001223
-
Somatic_Genetics_of_lesions_from_a_POT1_patient
Study
EGAS00001001343
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95664A
Dataset
EGAD00001004751
-
Korean Advanced Thyroid Cancer Dataset
Dataset
EGAD00001004845
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90560A
Dataset
EGAD00001004733
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95660A
Dataset
EGAD00001004750
-
Untargeted serum metabolomics profiled by Metabolon Inc.
Dataset
EGAD00001006247
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90706
Dataset
EGAD00001004744
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95632B
Dataset
EGAD00001004748
-
WGS samples for multiple myeloma (hipo-067 and hipo-K08K)
Dataset
EGAD00001008150
-
RNA-sequencing
Dataset
EGAD00001004784
-
MPNST_Data
Dataset
EGAD00001006253
-
Colorctal cancer WES/WGS analysis in Dr. Liu’s group in Sun Yat-sen University Cancer Center.
Dataset
EGAD00001003551
-
BBMRI - BIOS project - Freeze 2 - Fastq files - unrelated samples
Dataset
EGAD00001003785
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95670B
Dataset
EGAD00001004754
-
RNA sequencing data to study therapeutic targeting of ependymoma
Dataset
EGAD00001003966
-
SF11949 scRNA-Seq primary oligodendroglioma G3 IDH1 Mutant Male
Dataset
EGAD00001005397
-
SF12090 snRNA-Seq IDHR132H Wild-type Primary GBM Male
Dataset
EGAD00001005412
-
Sequencing data for oesophageal and related samples - Ococks, Frankell, Masque Soler et al (ctDNA)
Dataset
EGAD00001006373
-
Multiple Malignancy Familial Comparison
Dataset
EGAD00001001062
-
BLUEPRINT Methylome saturation and COMET analysis of monocyte samples
Dataset
EGAD00001001261
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A73044A
Dataset
EGAD00001004719
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A73044B
Dataset
EGAD00001004720
-
Genome-wide data of Erasmus Rucphen Family (ERF) Study
Dataset
EGAD00001003571
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95724B
Dataset
EGAD00001004757
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90554A
Dataset
EGAD00001004730
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90600C
Dataset
EGAD00001004735
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96150A
Dataset
EGAD00001004764
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A75617A
Dataset
EGAD00001004727
-
WES, ultra-deep sequencing exome and RNAseq data of diseased liver samples
Dataset
EGAD00001004792
-
BLUEPRINT September 2016, ATAC-seq for osteoclast from venous blood, on Genome GRCh38
Dataset
EGAD00001002907
-
EATL-II whole-exome sequencing profile
Dataset
EGAD00001002220
-
Exome sequencing of control DNA samples from patients with Waldenstrom macroglobulinemia
Dataset
EGAD00001005323
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A75616B
Dataset
EGAD00001004725
-
BLUEPRINT September 2016, ATAC-seq for naive B cell from tonsil, on Genome GRCh38
Dataset
EGAD00001002903
-
Paired-end RNA-seq analysis of the Hypermutation and Malignant Progression in Low-grade Glioma Patients
Dataset
EGAD00001005387
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95722A
Dataset
EGAD00001004755
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96139A
Dataset
EGAD00001004762
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96145A
Dataset
EGAD00001004763
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96156A
Dataset
EGAD00001004765
-
SF11964 snATAC Seq Low Grade Astrocytoma IDHR132H mutant
Dataset
EGAD00001005414
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90553A
Dataset
EGAD00001004728
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90553C
Dataset
EGAD00001004729
-
Lifelines-DEEP plasma un-targeted metabolomics 1054 baseline and 311 4-year followup
Dataset
EGAD00001006953
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95670A
Dataset
EGAD00001004753
-
single-cell RNA sequencing data of BALF and blood cells obtained from COPD patients and control donors
Dataset
EGAD00001006069
-
Sporadic Parathyroid Carcinoma
Dataset
EGAD00001000370
-
Whole genome sequencing of matched esophageal tumor-normal samples
Dataset
EGAD00001004832
-
Chromatin run-on and transcriptome sequencing of fibrolamellar carcinoma
Dataset
EGAD00001005797
-
RNAseq of resident memory T cells from human lung tumor
Dataset
EGAD00001006812
-
bulk RNA-seq of the 5 HCC patients which also have the single cell T cell RNA-seq data
Dataset
EGAD00001004148
-
Modulation of macrophage inflammatory function through selective inhibition of the epigenetic reader protein SP140
Dataset
EGAD00001006186
-
Genomic analysis of HPV-positive versus HPV-negative oesophageal adenocarcinoma
Dataset
EGAD00001001660
-
Evaluation of capture and amplicon-based targeted sequencing methods on formalin-fixed tumours
Dataset
EGAD00001006879
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95624A
Dataset
EGAD00001004747
-
A96240B
Dataset
EGAD00001007122
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95724A
Dataset
EGAD00001004756