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Whole genome bisufite sequencing of smoking and non-smoking mother-child pairsBisufite sequencing, RNA-seq and ChIP-Seq data of whole blood samples from smoking and non-smoking mothers and their children at gestation/birth and follow-up years.
Study
EGAS00001000455
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502 present-day genotypes included in the '137 ancient human genomes from across the Eurasian steppe' publication
Study
EGAS00001002926
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Genetic landscape of pediatric Infant Acute Lymphoblastic leukemia
Study
EGAS00001000246
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CCND1-negative MCL
Study
EGAS00001003060
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Primary breast cancers and paired brain metastases sequencing study
Study
EGAS00001003173
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DNA from colon cancer samples and matched normal samples was hybridized on Human 660W-Quad SNP arrays and sequenced in Illumina HiScanSQ.
Study
EGAS00001000558
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Role_of_Epigenetic_Memory_in_Human_Induced_Pluripotent_Stem_Cells_Pilot
Study
EGAS00001000742
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MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD37920__Targeted_
Study
EGAS00001003321
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Microsatellite unstable colorectal cancers
Study
EGAS00001003366
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Illumina Human OmniExpress genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000687
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Unraveling metastatic progression of breast cancer
Study
EGAS00001000760
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Molecular profiling of blastic plasmacytoid dendritic cell neoplasm (BPDCN) as compared to acute myeloid leukemia (AML)
Study
EGAS00001003453
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Alternative lengthening of telomeres in childhood neuroblastoma from genome to proteome
Study
EGAS00001004349
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Fetal hemoglobin in sickle cell disease patients from Tanzania
Study
EGAS00001000990
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Congenital_anosmia_1
Study
EGAS00001001124
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HipSci___RNAseq___Rare_Monogenic Diabetese
Study
EGAS00001001137
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Single-cell RNA-sequencing reveals that glioblastoma recapitulates a normal neurodevetlopmental hierarchy
Study
EGAS00001004422
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Understand_Paratyphoid_Disease___host_responses_to_human_challenge_with_S__Paratyphi_A
Study
EGAS00001001260
-
Characterization of four subtypes in morphologically normal tissue excised proximal and distal to breast cancer
Study
EGAS00001004510
-
SNP genotyping data in genes related to trace element homeostasis
Study
EGAS00001001292
-
Breast Cancer - Subtype defined by an amplification of the HER2 gene
Study
EGAS00001001431
-
Whole Genome Sequencing of 317 individuals from the Pacific region
Study
EGAS00001004540
-
Indonesian Genome Diversity Project 2
Study
EGAS00001003654
-
Single cell T cell Landscape and T Cell Receptor Repertoire Profiling of AML in Context of PD-1 Blockade Therapy
Study
EGAS00001004894
-
Ultraviolet radiation drives mutations in a subset of mucosal melanomas
Study
EGAS00001004697
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Genomics_of_acral_lentiginous_melanoma
Study
EGAS00001003740
-
HCA_Female_Reproductive_Adult_WSSS_RNA
Study
EGAS00001004727
-
NRG1 Fusions in KRAS Wild-type Pancreatic Cancer (H021)
Study
EGAS00001002759
-
Premalignant SOX2 overexpression in the fallopian tubes of ovarian cancer patients: Discovery and validation studies
Study
EGAS00001001909
-
Genomics_of_acral_lentiginous_melanoma___RNAseq
Study
EGAS00001003758
-
Transcriptome sequencing of intravenous leiomyomatosis and uterine myoma
Study
EGAS00001002504
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The aim of this study was to identify underlying hub genes and dysregulated pathways associated with the development of HCC using bioinformatics analysis.
Study
EGAS00001002526
-
Progression to AML is predictable and distinct from age related clonal hematopoiesis
Study
EGAS00001002570
-
NanoSring of PBMC from bladder cancer and RCC patients
Study
EGAS00001004229
-
Transcriptome profiling of human plucked frontal and occipital hair follicles
Study
EGAS00001002832
-
Exploring_the_heterogeneity_of_sarcoma_using_single_cell_sequencing_
Study
EGAS00001002866
-
Identification of hypermutation and defective mismatch repair in ctDNA from metastatic prostate cancer
Study
EGAS00001003899
-
Long cell-free DNA molecules in maternal plasma
Study
EGAS00001005515
-
Single cell exome sequencing of lung adenocarcinoma
Study
EGAS00001002972
-
Patterns of transcription factor programs and immune pathway activation define four major subtypes of SCLC with distinct therapeutic vulnerabilities
Study
EGAS00001004888
-
Whole exome sequencing on Pediatric MDS patients
Study
EGAS00001005432
-
Single-cell DNA sequencing on Pediatric MDS
Study
EGAS00001005433
-
Benchmarking of ProSolo, a new probabilistic single nucleotide variant caller for single cell DNA sequencing data. This study provides the whole exome sequencing dataset used in this assessment.
Study
EGAS00001004123
-
Panbody_nanoseq
Study
EGAS00001005521
-
COVID_19_UK_CIC_Spatial
Study
EGAS00001005817