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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
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96187A
Dataset
EGAD00001004770
-
Sequencing data for oesophageal and related samples - Katz-Summercorn, Jammula et al (RNA)
Dataset
EGAD00001006353
-
Mutation analysis of 17 genes in plasma DNA of CRC patients using the AVENIO ctDNA Targeted Kit
Dataset
EGAD00001006103
-
Variation and transmission of the human gut microbiota across generations - 16S data
Dataset
EGAD00001008195
-
2014_AML Whole genome sequencing analysis result
Dataset
EGAD00001003557
-
Whole genome sequence data from Illumina HiSeqX instruments
Dataset
EGAD00001003562
-
BBMRI - BIOS project - Freeze 2 - Bam files - GoNL samples
Dataset
EGAD00001003786
-
Personalised therapy with MEK inhibition leads to a sustained complete response in an adolescent patient with a recurrent malignant peripheral nerve sheath tumor
Dataset
EGAD00001006793
-
Transcriptome sequencing of replication repair deficient brain cancers
Dataset
EGAD00001006921
-
RNAseq of SCCOHT patient tumors
Dataset
EGAD00001007829
-
BLUEPRINT: A human variation panel of genetic influences on epigenomes and transcriptomes in three immune cells (WGS)
Dataset
EGAD00001002663
-
Somatic Genetics of lesions from a POT1 patient (2017-04-27)
Dataset
EGAD00001003307
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90694B
Dataset
EGAD00001004743
-
BBMRI - BIOS project - Freeze 2 - Bam files - Imprinting analysis
Dataset
EGAD00001003937
-
16S sequencing of intestinal biopsies
Dataset
EGAD00001003936
-
CYPTAM - PacBio SMRT sequencing
Dataset
EGAD00001005972
-
Merged single-cell RNA-seq data for 22 Hodgkin lymphomas and 5 reactive lymph nodes
Dataset
EGAD00001006221
-
Whole-exome sequencing and microRNA profiling predicted relapse risk of stage I lung adenocarcinomas
Dataset
EGAD00001006188
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires forlibrary A96176A
Dataset
EGAD00001004769
-
Dnase1l3 deletion causes aberrations in length and end-motif frequencies in plasma DNA
Dataset
EGAD00001005071
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95732A
Dataset
EGAD00001004759
-
Lung Multi-site Targeted Sequence Capture
Dataset
EGAD00001001017
-
Sequencing data for oesophageal and related samples - Rogerson et al (RNA)
Dataset
EGAD00001005915
-
Somatic mutation analysis based on Whole exome Sequencing (WES) of multiple tumor biopsies, patient-derived spheroids and leukocyte DNA from colorectal cancer patients (vcf files)
Dataset
EGAD00001003823
-
2016 AML prospective_v1 analysis result
Dataset
EGAD00001003928
-
Transcriptome profiling for Korean Early Onset Gastric Cancer
Dataset
EGAD00001002187
-
BLUEPRINT release August 2015, DNase-Hypersensitivity for monocyte, on genome GRCh38
Dataset
EGAD00001001560
-
Single cell Transcriptome Analysis of regulatory Tcells from blood, fat and skin
Dataset
EGAD00001007665
-
Japanese liver cancer RNAseq
Dataset
EGAD00001001880
-
FACS-based purification and paired-end RNA sequencing
Dataset
EGAD00001007687
-
WGS data of colorectal cancer patients
Dataset
EGAD00001007746
-
BRIDGE SPEED April 2016
Dataset
EGAD00001002070
-
GenomeDenmark Phase 2 - variants called on chrY for 62 males.
Dataset
EGAD00001003186
-
BLUEPRINT September 2016, ATAC-seq Multiple Myeloma for plasma cell from bone marrow, on Genome GRCh38
Dataset
EGAD00001002920
-
Exome sequencing of samples taken at multiple timepoints of AML patients
Dataset
EGAD00001002728
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90685
Dataset
EGAD00001004738
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96156B
Dataset
EGAD00001004766
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96165A
Dataset
EGAD00001004767
-
Whole genome sequencing generated from 11 glioma patient samples
Dataset
EGAD00001007771
-
The dataset of breast cancer patients and benign breast tumor patients
Dataset
EGAD00001004175
-
sQTL summary statistics
Dataset
EGAD00001005042