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Analysis of DNA methylation in normal B cells and chronic lymphocytic leukemia
Study
EGAS00001000534
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Extensive three-dimensional intratumor proteomic heterogeneity revealed by multiregion sampling in high-grade serous ovarian tumor specimens
Study
EGAS00001005786
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Biallelic HMBS Inactivation Defines a Homogenous Clinico-Molecular Subtype of Hepatocellular Carcinoma
Study
EGAS00001005986
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Clonal hematopoiesis is associated with adverse outcomes in patients with COVID-19
Study
EGAS00001006218
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Genomes of Relapsing Neuroblastoma
Study
EGAS00001001387
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Long-read sequencing of diagnosis and post-therapy medulloblastoma reveals complex rearrangement patterns and epigenetic signatures
Study
EGAS00001006576
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DNA methylation atlas of normal human cell types
Study
EGAS00001006791
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Interactions between the tumor and the systemic response of breast cancer patients
Study
EGAS00001001804
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Lineage-specific genome architecture links disease variants to target genes
Study
EGAS00001001911
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Genomic Analyses Identify Recurrent MEF2D Fusions in Acute Lymphoblastic Leukemia
Study
EGAS00001001952
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HipSci - Human Induced Pluripotent Stem Cells Initiative
Study
EGAS00001001465
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APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UGWAS component)
Study
EGAS00001001558
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Mutant KIT as imatinib-sensitive target in metastatic sinonasal carcinoma (H021)
Study
EGAS00001001845
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CD36 defines CML cells less sensitive to imatinib
Study
EGAS00001002421
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TGF-β attenuates tumour response to PD-L1 blockade by contributing to exclusion of T cells.
Study
EGAS00001002556
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Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
Study
EGAS00001000369
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Mutational analysis reveals the origin and therapy-driven evolution of recurrent glioma
Study
EGAS00001000579
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Genome-wide SNP genotyping of Central African rainforest hunter-gatherers and neighbouring agriculturalists
Study
EGAS00001000605
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Study of pediatric hepatocellular carcinoma caused by bile salt export pump deficiency
Study
EGAS00001000749
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Ovarian cancer organoid biobank
Study
EGAS00001003073
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CPC-GENE Prostate Cancer Heterogeneity Study
Study
EGAS00001000549
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Inference of transcription factor binding from cell-free DNA enables tumor subtype prediction and early detection
Study
EGAS00001003206
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Exome-seq, RNA-Seq, SNP array profiling of gastric tumor samples and cell lines.
Study
EGAS00001000736
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Assessment_of_epigenetic_variation_in_human_iPS_cells_Medip
Study
EGAS00001000741
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Recursive splicing in long vertebrate genes
Study
EGAS00001001170
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Uveal melanoma patient with germline MBD4 nonsense mutation
Study
EGAS00001003362
-
Illumina HumanCoreExome genotyping data from the British Society for Surgery of the Hand Genetics of Dupuytren’s Disease consortium (BSSH-GODD consortium) collection
Study
EGAS00001001206
-
MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
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Engineering of a promoterless anti-viral RNAi hairpin into an endogenous miRNA locus
Study
EGAS00001001252
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Analysis of four key cell types (epithelial, fbroblast, myeloid and T cells)
Study
EGAS00001003579
-
Mitochondrial-Nuclear Mutational Cross-Talk Drives Recurrence of Localized Prostate Cancer
Study
EGAS00001001782
-
Whole Genome Sequencing of Gingivo-buccal Cancer: ICGC-India Project_YR03
Study
EGAS00001001901
-
METABRIC: Data from Pereira et al (2016), The somatic mutation profiles of 2433 breast cancers refine their genomic and transcriptomic landscapes. Nat Comms 7.
Study
EGAS00001001753
-
Sequencing_Acute_Myeloid_Leukaemia_
Study
EGAS00001000035
-
Immunogenomics of colorectal cancer response to immune checkpoint blockade
Study
EGAS00001004438
-
Targeted sequencing of Burkitt lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001004649
-
Mesenchymal inflammation drives genotoxic stress in hematopoietic stem cells and predicts disease evolution in human pre-leukemia
Study
EGAS00001001926
-
RNA-seq study of a Princess Margaret Cancer Centre human acute myeloid leukemia patient cohort
Study
EGAS00001004792
-
Gene fusion and transcriptomic landscapes of sarcomas
Study
EGAS00001002189
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Scalable whole-genome single-cell library preparation without pre-amplification
Study
EGAS00001002170
-
Clinical Cancer Genomic Profiling by Three-Platform Sequencing of Whole Genome, Whole Exome and Transcriptome
Study
EGAS00001002217
-
Drug screening and whole genome sequencing of primary cells and cell lines from ovarian cancer patients to associate genomic aberrations with in vitro drug sensitivities
Study
EGAS00001002239
-
Population_dynamics_in_abnormal_haematopoiesis
Study
EGAS00001003181
-
Mechanisms_of_patient_response_to_Dabrafenib_in_Melanoma
Study
EGAS00001000946
-
This study explored and validated the clinical application of targeted NGS of circulating tumor DNA in identifying tumor-specific mutations and uncovering clinical actionable targets in a variety of solid tumors in large patient cohorts.
Study
EGAS00001002251