-
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
-
Tam-seq of germline samples for HGSOC copy-number signatures study
Dataset
EGAD00001004172
-
Somatic mutations in epithelial cells from endometriosis and normal uterine endometrium
Dataset
EGAD00001004186
-
Evolution of neoantigen landscape during immune checkpoint blockade in non-small cell lung cancer
Dataset
EGAD00001004336
-
Epi2Diag raw methylation array data for patients with neurodevelopmental disorders
Dataset
EGAD00010002724
-
Whole genome sequencing of C1498 cells.
Dataset
EGAD50000001826
-
The landscape of LAM disease
Study
EGAS00001003534
-
Non-coding RNAs in breast cancer
Study
EGAS00001003353
-
Bioinformatics analysis of chimerism in monochorionic dizygotic twins
Study
EGAS00001005997
-
Kidney_Single_Cell_Study
Study
EGAS00001002325
-
MNM - Temporal variability in Quantitative Microbiome Profiles
Study
EGAS00001005686
-
Exome and transcriptome sequencing of Desmoplastic Small Round Cell Sarcoma
Study
EGAS00001004575
-
Co-infection of fungi and bacteria in brain tissue of Alzheimer’s patients.
Study
EGAS00001002766
-
The integrated genomic and immune landscapes of lethal metastatic breast cancer.
Study
EGAS00001002703
-
Genomic and transcriptomic profiling of combined hepatocellular and intrahepatic cholangiocarcinoma reveals distinct molecular subtypes
Study
EGAS00001003093
-
The polarity and specificity of antiviral T lymphocyte responses determine susceptibility to SARS-CoV-2 infection in cancer patients and healthy individuals.
Study
EGAS00001005985
-
The_Little_Princess_Knowledge_Bank_
Study
EGAS00001004237
-
CD8+ Tumor-Infiltrating Lymphocyte Abundance is a Positive Prognostic Indicator in Nasopharyngeal Cancer
Study
EGAS00001006396
-
Multiomic profiling of early-passage melanoma cell lines.
Study
EGAS00001004536
-
Whole-genome landscape of adult T-cell leukemia/lymphoma
Study
EGAS00001005237
-
Organoid_Derivation_Project___GRCh38___RNAseq
Study
EGAS00001004677
-
Single-cell RNA sequencing of bronchoalveolar lavages from COVID-19 patients
Study
EGAS00001004717