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Breast_Cancer_Somatic_Genetics_Study_
Study
EGAS00001000195
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ENGAGE___Amendment__500_genes_exon_sequencing_
Study
EGAS00001000137
-
Radiotherapy_induced_sarcoma
Study
EGAS00001000138
-
High_powered_complex_trait_association_mapping_through_whole_genome_sequencing_of_a_selected_subpopulation_of_the_INGI_Val_Borbera_genetic_isolate
Study
EGAS00001000398
-
DKFZ-HIPO Project H021/NCT MASTER
Study
EGAS00001000948
-
Signatures of Aristolochic Acid Mutagenesis in Bladder Cancer
Study
EGAS00001000975
-
MDS Sequencing Project_Cancer Cell
Study
EGAS00001001011
-
Platelet_collagen_defect
Study
EGAS00001000105
-
V2_panel_bait_design_test
Study
EGAS00001001780
-
Integrated molecular analysis of adult T-cell leukemia/lymphoma
Study
EGAS00001001296
-
Glioblastoma_CRISPR_Screen
Study
EGAS00001001519
-
ENU_HT_29_BRAF_Triple_Therapy_Clones
Study
EGAS00001001778
-
Signatures of mismatch repair deficiency in cancer genomes
Study
EGAS00001000182
-
HipSci_RNASEQ_Usher syndrome and congenital eye defects
Study
EGAS00001001997
-
Post-zygotic germline mutations in sperm
Study
EGAS00001001700
-
120 individuals from the TEENAGE study (Ntalla et al., 2013) have been genotyped on the Illumina HumanCoreExome-12v1-1_A array. This is a population-based study of adolescents from the Attica region in Greece
Study
EGAS00001001733
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We performed whole exome sequencing (WES) using Hiseq on 22 paired CMLs. We also performed whole exome sequencing (WES) using CG on 88 paired CMLs. All the data belongs to CML in China - ICGC project.
Study
EGAS00001001742
-
Human_Evolution_3
Study
EGAS00001000315
-
Australia_and_New_Guinea_haplotype_phasing_
Study
EGAS00001001853
-
Melanoma_brain_metastases
Study
EGAS00001002107
-
BLUEPRINT release August 2016, ChIP-Seq for monocyte - RPMI_T=24hrs, on genome GRCh38
Dataset
EGAD00001002474
-
BLUEPRINT release August 2016, ChIP-Seq for monocyte - RPMI_LPS_T=24hrs, on genome GRCh38
Dataset
EGAD00001002388
-
BLUEPRINT release August 2016, ChIP-Seq for conventional dendritic cell, on genome GRCh38
Dataset
EGAD00001002310
-
Bam files from Whole exome sequencing (WES, ~50x mean read depth) of metachronous bladder tumors
Dataset
EGAD00001002716
-
MASQ targeted amplicon sequencing data of AML samples at presentation, remission, and relapse, and MASQ data demonstrating performance ranges of the method.
Dataset
EGAD00001005121
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Regulatory T cell transcriptomic reprogramming characterizes adverse events by checkpoint inhibitors in solid tumors
Dataset
EGAD00001006415
-
BLUEPRINT release August 2016, RNA-Seq for memory B cell, on genome GRCh38
Dataset
EGAD00001002347
-
Assessment of genetic and epigenetic variation in human IPS cells
Dataset
EGAD00001000384
-
BLUEPRINT release August 2016, ChIP-Seq for unswitched memory B cell, on genome GRCh38
Dataset
EGAD00001002282
-
Mapping genetic variants underlying gene regulation in healthy intestinal cell types to identify novel IBD drug targets (2020-05-12)
Dataset
EGAD00001006139
-
BLUEPRINT release January 2015, RNA-Seq for endothelial cell of umbilical vein (resting)
Dataset
EGAD00001001142
-
BLUEPRINT release August 2016, ChIP-Seq for CD8-positive, alpha-beta thymocyte, on genome GRCh38
Dataset
EGAD00001002494
-
BLUEPRINT release August 2016, RNA-Seq for Acute Promyelocytic Leukemia - MS-275 (20h), on genome GRCh38
Dataset
EGAD00001002500
-
BLUEPRINT release August 2016, ChIP-Seq for monocyte - T=0days, on genome GRCh38
Dataset
EGAD00001002491