-
BLUEPRINT release January 2015, RNA-Seq for cytotoxic CD56-dim natural killer cell
Dataset
EGAD00001001159
-
Expression quantitative trait locus mapping in human pancreatic islets of Langerhans
Dataset
EGAD00001001601
-
High-throughput sequencing data of immunoglobulin gene rearrangements in acute lymphoblastic leukaemia - summary .fastq and .bcl files
Dataset
EGAD00001001983
-
BLUEPRINT release August 2016, ChIP-Seq for monocyte - Attached_T=1hr, on genome GRCh38
Dataset
EGAD00001002415
-
Non-ADT METs ICGC Prostate UK
Dataset
EGAD00001002002
-
ENU-LS-411N-TripleTherapy
Dataset
EGAD00001002051
-
BLUEPRINT September 2016, ChIPmentation for mature conventional dendritic cell GM-CSF_IL4_T=6_days_R848_T=24hrs from venous blood, on Genome GRCh38
Dataset
EGAD00001002941
-
BLUEPRINT September 2016, ChIPmentation Activated B-Cell-Like Diffuse Large B-Cell Lymphoma from lymph node, on Genome GRCh38
Dataset
EGAD00001002944
-
BLUEPRINT September 2016, ChIPmentation for effector memory CD8-positive, alpha-beta T cell from venous blood, on Genome GRCh38
Dataset
EGAD00001002945
-
BLUEPRINT September 2016, ChIPmentation Germinal Center B-Cell-Like Diffuse Large B-Cell Lymphoma from lymph node, on Genome GRCh38
Dataset
EGAD00001002946
-
BLUEPRINT September 2016, ChIP-Seq for conventional dendritic cell from cord blood, on Genome GRCh38
Dataset
EGAD00001002948
-
BLUEPRINT September 2016, ChIP-Seq Acute Lymphocytic Leukemia for precursor B cell from venous blood, on Genome GRCh38
Dataset
EGAD00001002949
-
BLUEPRINT September 2016, ChIP-Seq for memory B cell from venous blood, on Genome GRCh38
Dataset
EGAD00001002950
-
BLUEPRINT September 2016, ChIP-Seq T-cell Acute Lymphocytic Leukemia from capillary blood, on Genome GRCh38
Dataset
EGAD00001002952
-
BLUEPRINT September 2016, RNA-Seq Acute Lymphocytic Leukemia for precursor B cell from bone marrow, on Genome GRCh38
Dataset
EGAD00001002953
-
BLUEPRINT September 2016, RNA-Seq for monocyte T=0day from venous blood, on Genome GRCh38
Dataset
EGAD00001002955
-
BLUEPRINT September 2016, RNA-Seq T-cell lymphoma for helper T cell from venous blood, on Genome GRCh38
Dataset
EGAD00001002956
-
BLUEPRINT September 2016, RNA-Seq for monocyte T=2day_RANK_M-CSF from venous blood, on Genome GRCh38
Dataset
EGAD00001002957
-
BLUEPRINT September 2016, RNA-Seq for monocyte T=1day_M-CSF_S100A9_4hr_RANL from venous blood, on Genome GRCh38
Dataset
EGAD00001002959
-
BLUEPRINT September 2016, RNA-Seq for monocyte T=6day_S100A9_RANKL_M-CSF from venous blood, on Genome GRCh38
Dataset
EGAD00001002960
-
BLUEPRINT September 2016, RNA-Seq for monocyte T=10day_S100A9_RANKL_M-CSF from venous blood, on Genome GRCh38
Dataset
EGAD00001002961
-
BLUEPRINT September 2016, RNA-Seq Acute Myeloid Leukemia for blast cell from bone marrow, on Genome GRCh38
Dataset
EGAD00001002962
-
BLUEPRINT September 2016, RNA-Seq Acute Lymphocytic Leukemia for precursor B cell from venous blood, on Genome GRCh38
Dataset
EGAD00001002963
-
BLUEPRINT September 2016, RNA-Seq for monocyte T=1day_4hr_RANK from venous blood, on Genome GRCh38
Dataset
EGAD00001002964
-
BLUEPRINT September 2016, RNA-Seq for monocyte T=2day_S100A9_RANKL_M-CSF from venous blood, on Genome GRCh38
Dataset
EGAD00001002965
-
BLUEPRINT September 2016, RNA-Seq for monocyte T=10day_RANK_M-CSF from venous blood, on Genome GRCh38
Dataset
EGAD00001002966
-
BLUEPRINT September 2016, RNA-Seq for monocyte T=6day_RANK_M-CSF from venous blood, on Genome GRCh38
Dataset
EGAD00001002967
-
BLUEPRINT September 2016, RNA-Seq Acute Myeloid Leukemia for myeloid cell from venous blood, on Genome GRCh38
Dataset
EGAD00001002968
-
Whole-genome and transcriptome sequencing of NUT midline carcinoma
Dataset
EGAD00001003117
-
Multiple Myeloma Diagnosis to Relapse study samples (2017-04-27)
Dataset
EGAD00001003309
-
Indonesian Genome Diversity Project
Dataset
EGAD00001004156
-
Deep WGS of matched tumor-normal pairs for HGSOC copy-number signatures study
Dataset
EGAD00001004189
-
Dataset Plasma-seq
Dataset
EGAD00001000364
-
Myeloproliferative Disease Whole Genomes
Dataset
EGAD00001000385
-
Myelodysplastic syndrome whole genomes
Dataset
EGAD00001000386
-
Identification of low frequency variants associated with ulcerative colitis using whole-genome sequencing
Dataset
EGAD00001000409
-
Deep sequencing analysis of human iPSC-specific SNVs in donor cell population
Dataset
EGAD00001000605
-
Whole exome sequencing of young onset Primary Sclerosing Cholangitis
Dataset
EGAD00001000671
-
Sequencing probands and families with severe insulin resistance syndromes
Dataset
EGAD00001000694
-
BLUEPRINT release August 2014, RNA-Seq for CD8-positive, alpha-beta T cell
Dataset
EGAD00001000912
-
BLUEPRINT release January 2015, ChIP-Seq for endothelial cell of umbilical vein (proliferating)
Dataset
EGAD00001001136
-
BLUEPRINT release January 2015, RNA-Seq for CD14-positive, CD16-negative classical monocyte
Dataset
EGAD00001001148
-
BLUEPRINT release January 2015, ChIP-Seq for cytotoxic CD56-dim natural killer cell
Dataset
EGAD00001001158
-
BLUEPRINT release January 2015, RNA-Seq for effector memory CD4-positive, alpha-beta T cell
Dataset
EGAD00001001163
-
BLUEPRINT release January 2015, RNA-Seq for central memory CD4-positive, alpha-beta T cell
Dataset
EGAD00001001172
-
BLUEPRINT release January 2015, ChIP-Seq for CD38-negative naive B cell
Dataset
EGAD00001001207
-
Fastq data for ChIP-Seq (H3K4me3) assays for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001407
-
RNASeq_EGAS00001001306
Dataset
EGAD00001001443
-
BLUEPRINT release August 2015, ChIP-Seq for naive B cell, on genome GRCh38
Dataset
EGAD00001001519
-
BLUEPRINT release August 2015, RNA-Seq for class switched memory B cell, on genome GRCh38
Dataset
EGAD00001001531
-
BLUEPRINT release August 2015, RNA-Seq for memory B cell, on genome GRCh38
Dataset
EGAD00001001542
-
BLUEPRINT release August 2015, ChIP-Seq for adult endothelial progenitor cell, on genome GRCh38
Dataset
EGAD00001001554
-
BLUEPRINT release August 2015, ChIP-Seq for macrophage, on genome GRCh38
Dataset
EGAD00001001576
-
BLUEPRINT release August 2015, ChIP-Seq for segmented neutrophil of bone marrow, on genome GRCh38
Dataset
EGAD00001001588
-
March 2016 update of smRNA-Seq assays data (bam/fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001959
-
BLUEPRINT release August 2016, ChIP-Seq for monocyte - T=10day_RANK_M-CSF, on genome GRCh38
Dataset
EGAD00001002420
-
BLUEPRINT release August 2016, ChIP-Seq for naive B cell, on genome GRCh38
Dataset
EGAD00001002466
-
BLUEPRINT release August 2016, ChIP-Seq for endothelial cell of umbilical vein (resting), on genome GRCh38
Dataset
EGAD00001002488
-
Comparison of protocols for deriving pancreatic progenitors from hPSCs (ATAC-seq)
Dataset
EGAD00001004824
-
Healthy human B-lymphopoiesis RNA-Seq reference using FACS sorted bone marrow aspirates
Dataset
EGAD00001010917
-
RNA sequencing of in vitro generated suppressive myeloid cells using parental and Sialidase expressing A549 cancer cell lines
Dataset
EGAD00001012437
-
Whole genome sequencing of tumor samples from advanced pre-treated NSCLC patients recruited in a phase I/II single-arm trial utilising CVA21, an oncolytic coxsackie virus, in combination with pembrolizumab.
Dataset
EGAD00001015682
-
ATAC-Seq/Hi-C/4C-Seq dataset for Malignant rhabdoid study
Dataset
EGAD00001011820
-
BLUEPRINT release August 2016, RNA-Seq for colony forming unit erythroid, on genome GRCh38
Dataset
EGAD00001002509
-
Comparison of 3 protocols for deriving pancreatic progenitors from hPSCs (RNA-seq)
Dataset
EGAD00001004823
-
Pervasive H3K27 acetylation and ERV expression in H3.3K27M gliomas present a therapeutic vulnerability
Dataset
EGAD00001004961
-
Targeted gene panel sequencing of matched diagnosis-remission-relapse B cell precursor acute lymphoblastic leukemia samples
Dataset
EGAD00001004977
-
Genomic Signatures Reveal DNA Damage Response Deficiency in Brain Metastases of Colorectal Cancer
Dataset
EGAD00001005030
-
Next Generation Sequencing Characterization of Hematopoietic Stem and Progenitors Cells in Human Systemic Lupus Eryhtematosus
Dataset
EGAD00001005052
-
V(D)J and 5' Gene Expression data of bone marrow cells from patients with aplastic anemia
Dataset
EGAD00001012117
-
Reference exome data for Australian Aboriginal populations from Western Australia and the Northern Territory
Dataset
EGAD00001005189
-
Raw FASTQ files from TSO500 hybrid capture sequencing of prostate cancer tissue and plasma.
Dataset
EGAD50000002463
-
Sequencing data for oesophageal and related samples - Noorani et al (WGS)
Dataset
EGAD00001005434
-
Small RNA-sequencing and RNA-sequencing data of tuberous sclerosis complex subependymal giant cell astrocytomas
Dataset
EGAD00001005932
-
Somatic mutation and clonal evolution in the human bladder_WGS (2020-05-05)
Dataset
EGAD00001006113
-
RNA sequencing of human intra- and extracranial endothelial cells
Dataset
EGAD00001006203
-
WES data from 165 tumor/germline samples with muscle invasive bladder cancer.
Dataset
EGAD00001006239
-
Detection of ctDNA in Plasma of Patients with Clinically Localised Prostate Cancer is Associated with Rapid Disease Progression
Dataset
EGAD00001006369
-
WGS and WES of Advance Prostate Cancer
Dataset
EGAD00001006487
-
Resequencing (MIPS) of candidate genes for Keratoconus (2020)
Dataset
EGAD00001006825
-
Sequencing data for oesophageal and related samples - Nowicki-Osuch, Zhuang et al (bulk RNA)
Dataset
EGAD00001006882
-
VCF file from 16 patients affected by acute intermittent porphyria
Dataset
EGAD00001006952
-
cfMeDIP data for 67 VPC samples
Dataset
EGAD00001008711
-
The dataset for Detecting Liver Cancer Using Cell-Free DNA Fragmentomes
Dataset
EGAD00001010931
-
limbal stem cells from Aniridia patients
Dataset
EGAD00001011124
-
To profile the landscape of sebaceous tumours_WES
Dataset
EGAD00001015367
-
RNA-seq dataset of Characterization of UV DNA damage in B-cell precursor acute lymphoblastic leukemia
Dataset
EGAD00001015598
-
Combining dasatinib and IFN-α in CML – immunomodulatory effects linked to treatment response and adverse events
Study
EGAS00001005049
-
Genome-wide gene expression analysis following CRISPRi of transposable elements
Study
EGAS00001008265
-
Piloting exome resequencing in consanguineous families with homozygosity mapping intervals
Study
EGAS00001000024
-
Kaposi_sarcoma_exome
Study
EGAS00001000032
-
_WGS__Somatic_mutation_in_skin_epidermis__SMS_
Study
EGAS00001004464
-
Chondrosarcoma_Targeted_Sequencing_Study
Study
EGAS00001000277
-
A common single nucleotide variant in T is strongly associated with chordoma
Dataset
EGAD00001000226
-
SCAT_Osteosarcoma_Validation
Dataset
EGAD00001000280
-
SC_DDD-G-4
Dataset
EGAD00010001604
-
Exploiting evolutionary steering in cancer therapy
Dataset
EGAD00001005782
-
NGS on cardiac samples in Hungarian patients of dilated cardiomyopathy
Study
EGAS50000000049
-
Targeted sequencing (paired) of HR genes in primary and metastatic patient-derived xenografts (PDXs) of colorectal cancer (CRC)
Dataset
EGAD50000000107
-
AVENIO Expanded ctDNA panel sequence alignments (BAMs)
Dataset
EGAD50000000138