-
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
-
CBD-RAW-REPERTOIRE-B: B cell bulk repertoire sequence files
Dataset
EGAD00001007960
-
Breast implant-associated anaplastic large cell lymphoma shallow whole genome sequencing for copy number analysis and Whole exome sequencing data.
Dataset
EGAD00001006433
-
Matched Pair Cell Line Tumour RNAseq
Dataset
EGAD00001000630
-
DKFZ-St.Jude Medulloblastoma - 225 clinical cases, control exomes with some paired tumor.
Dataset
EGAD00001006665
-
Whole exome DNA sequencing data of pretreatment tumor biopsies and matched blood samples of patients treated in the OpACIN-neo trial
Dataset
EGAD00001006730
-
CBD-RAW-SC-VDJ-T: 10X Single-Cell VDJ TCR
Dataset
EGAD00001007965
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90560B
Dataset
EGAD00001004734
-
200PG : WGS Aligned Sequence (fastq)
Dataset
EGAD00001003139
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90689A
Dataset
EGAD00001004739
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90648B
Dataset
EGAD00001004736
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90694A
Dataset
EGAD00001004742
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95736A
Dataset
EGAD00001004761
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96171A
Dataset
EGAD00001004768
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A75616A
Dataset
EGAD00001004724
-
BLUEPRINT September 2016, ATAC-seq for plasma cell from tonsil, on Genome GRCh38
Dataset
EGAD00001002912
-
2015 AML-ETO WGS analysis result
Dataset
EGAD00001004011
-
16S sequencing from feces
Dataset
EGAD00001003935
-
clonealign: 10X genomics chromium single-cell RNA-sequencing
Dataset
EGAD00001004552
-
Longitudinal breast cancer cohort in SMC
Dataset
EGAD00001004487
-
Whole genome sequencing of paired samples from primary and relapsed IDH-wt glioblastomas with matched blood controls
Dataset
EGAD00001004563
-
LifeLines-DEEP 4 years follow-up 338 MGS
Dataset
EGAD00001006959
-
SF4297 snRNA-Seq Primary GBM
Dataset
EGAD00001005415
-
Somatic pseudogenes acquired during cancer development – RNAseq
Dataset
EGAD00001000639
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90554B
Dataset
EGAD00001004731
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A75616C
Dataset
EGAD00001004726
-
Papuan Genomes: high depth (30x) whole genome sequence data
Dataset
EGAD00001001634
-
Whole-genome sequencing data for inflammatory breast cancer patients
Dataset
EGAD00001005749
-
Transcriptomic origins of mpMRI visibility
Dataset
EGAD00001004397
-
Whole Exome Sequencing
Dataset
EGAD00001004503
-
SF10022 snRNA-Seq Primary High-grade Glioma
Dataset
EGAD00001005409
-
Somatic copy-number alterations in plasma circulating tumor DNA from advanced EGFR-mutated lung adenocarcinoma patients
Dataset
EGAD00001007505
-
BLUEPRINT release January 2015, RNA-Seq for monocyte
Dataset
EGAD00001001191
-
sn-RNAseq profiling of the impact of a cytokine storm model in human cardiac organoids
Dataset
EGAD00001007533
-
RNA Seq Data
Dataset
EGAD00001001306
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90682
Dataset
EGAD00001004737
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90689C
Dataset
EGAD00001004741
-
Latency and interval therapy affect the evolution in metastatic colorectal cancer
Dataset
EGAD00001005226
-
WGS of off-target analysis of prime editing in organoids
Dataset
EGAD00001007744
-
There are 22 pairs of LAML cases in this project which belongs to LAML-CN. The library is constructed by the Illumina protocol.
Dataset
EGAD00001003317
-
BBMRI - BIOS project - Freeze 2 - Bam files - unrelated samples
Dataset
EGAD00001003784
-
Whole Exome Sequencing of a Melanoma Patient with Acquired Resistance to MEK plus CDK4/6 Inhibition
Dataset
EGAD00001003989
-
Genomic Landscape of Radiation Induced Meningiomas
Dataset
EGAD00001004358
-
Whole-exome sequencing of additional thyroid disease cases (2015-08-05)
Dataset
EGAD00001001460
-
ICR_RNASeq_pHGG
Dataset
EGAD00001004116
-
Maternal plasma data in FetalQuantSD accurate quantification of fetal DNA fraction by shallow-depth sequencing of maternal plasma DNA
Dataset
EGAD00001004324
-
Vγ9Vδ2-T cells in chronic lymphocytic leukemia patients and healthy controls
Dataset
EGAD00001004325
-
RNA-seq normal adjacent colon NKI-AvL TGO series NGS-ProToCol
Dataset
EGAD00001004057
-
Kidney Single Cell Study (2018-08-20)
Dataset
EGAD00001004304
-
Carcinoid study - WGS dataset
Dataset
EGAD00001000813
-
Single-cell Transcriptome for glioblastoma intra-tumoral heterogeneity
Dataset
EGAD00001002249
-
Exome sequencing in patients with Oliver McFarlane Syndrome
Dataset
EGAD00001001042
-
BLUEPRINT release January 2015, DNase-Hypersensitivity for macrophage
Dataset
EGAD00001001198
-
Colonbiome shot-gun metagenomics
Dataset
EGAD00001010068
-
BASIS BC WGS Dataset
Dataset
EGAD00001001337
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90689B
Dataset
EGAD00001004740
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95664B
Dataset
EGAD00001004752
-
Exome sequencing in bipolar disorder families
Dataset
EGAD00001004276
-
Colorectal organoids and tumoroids - pulldown (2018-08-13)
Dataset
EGAD00001004292
-
Sequencing files for "Transcriptional Mechanisms of Resistance to Anti-PD-1 Therapy"
Dataset
EGAD00001003200
-
WGS of 4 childhood T-ALL patients - tumor and remission
Dataset
EGAD00001003951
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95621B
Dataset
EGAD00001004745
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95632D
Dataset
EGAD00001004749
-
Exome sequencing files for "A single mutant clone populates the pancreatic ductal system to generate coexisting neoplastic lesions"
Dataset
EGAD00001004044
-
Verification of BCR reconstruction from single-cell RNA-seq using BraCeR
Dataset
EGAD00001004199
-
Dataset for whole exome sequencing of 49 tumor-blood pairs and transcriptome sequencing of 44 tumors for adrenocortical tumors
Dataset
EGAD00001000810
-
BLUEPRINT release August 2014, DNase-Hypersensitivity for macrophage
Dataset
EGAD00001000931
-
20191008_EGA_MELA_Uveal_WGS
Dataset
EGAD00001005454
-
H3Africa ReMAC Shotgun Metagenomic Phenotype
Dataset
EGAD00001006244
-
WES data of colorectal cancer patients
Dataset
EGAD00001007745
-
Multi-sample whole exome sequencing from 4 cases of advanced breast cancer.
Dataset
EGAD00001003137
-
Warm_Autopsy_Single_Cell_X10
Dataset
EGAD00001003240
-
There are 66 pairs of LAML cases(complete genomics) in this project which belongs to LAML-CN.The library is constructed by the Completes Genomics protocol.
Dataset
EGAD00001003310
-
2015_AML Whole exome sequencing analysis result
Dataset
EGAD00001003587
-
Tel Aviv RNA-seq dataset of of BiPSCs and FiPSCs derived cells
Dataset
EGAD00001003780
-
BBMRI - BIOS project - Freeze 2 - Fastq files - GoNL samples
Dataset
EGAD00001003787
-
2018 AML-ETO WGS analysis result
Dataset
EGAD00001003912
-
RNA sequencing of human fetal brain at 7, 9, 12, 15 and 21 gestational weeks
Dataset
EGAD00001003915
-
2014 sequenced AML-WGS analysis result
Dataset
EGAD00001003925
-
Single-cell RNA sequencing on 12346 single T cells from 14 non-small cell lung cancer (NSCLC) patients
Dataset
EGAD00001003999
-
Low-coverage Whole Genome Sequencing, normal adjacent colon NKI-AvL TGO series NGS-ProToCol
Dataset
EGAD00001004094