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MutWP6__CRUK_Grand_Challenge_Mutographs_of_Cancer__Botseq
Study
EGAS00001004330
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Sensitive neoantigen discovery by real-time mutanome-guided immunopeptidomics - WES
Study
EGAS50000000976
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Dual inhibition of FLT3 and BCL-2 is effective in preclinical models of BCL11B-activated lineage ambiguous leukemia
Study
EGAS50000000978
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Single cell RNA sequencing of human embryonic forebrain after slice culturing for between four weeks and one month
Study
EGAS50000001185
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CLL Genome
Study
EGAS00000000092
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Hofer et al., A specific subpopulation of cancer-associated fibroblasts promotes resistance to chemotherapy in triple-negative breast cancer by upregulating G0S2 protein
Study
EGAS50000000886
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Tumor inflammation and mutational burden are differentially associated with response to nivolumab or nivolumab plus ipilimumab in metastatic colorectal cancer
Study
EGAS50000000416
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ucfDNA workflows for molecular profiling of malignant disease
Study
EGAS50000001093
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Processing of tissue and cfDNA samples of CRC patients using Active-seq
Study
EGAS50000001226
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Dynamic human admixture histories over the past ~1,300 years at the northern Himalayan frontier
Study
EGAS50000001342
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Spatial Dynamics of the Developing Human Heart
Study
EGAS50000001122
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Spatial Dynamics of the Developing Heart (single-cell)
Study
EGAS50000001029
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Maturation of Human Intestinal Epithelial Cell Layers Fortifies the Apical Surface against Salmonella Attack
Study
EGAS50000001241
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T cell receptor repertoire in cell-free DNA as a proxy for tumor infiltrates in patients treated with pembrolizumab
Study
EGAS50000001306
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Bulk RNA sequencing of day 2 and day 7 biopsies from the tuberculin skin test in people with latent tuberculosis, and of day 2 biopsies from saline controls
Dataset
EGAD50000001208
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TONIC-Trial-cfDNA-Project
Study
EGAS50000001308
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Single-cell Kinnex sequencing of Alzheimer's disease isoform profile
Study
EGAS50000001476
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Delineation of the heterogeneous molecular landscape of HRS cells and their biological contributions to forming comprehensive TME ecosystems.
Study
EGAS00001008064
-
A tumor-associated photoreceptor signature unifies distinct central nervous system malignancies
Study
EGAS50000001457
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Common origin and somatic mutation patterns of composite lymphomas and leukemias
Study
EGAS50000001017
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Single Cell RNA Transcriptomics of Mantle Cell Lymphoma Reveals the Presence of Treatment-Resistant Subclones at the Time of Diagnosis
Study
EGAS50000000825
-
Exome sequencing in HIV+ Viremic Non-Progressors (VNPs) and HIV+ Progressors
Study
EGAS50000000079
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Measles oncolytic virus as an immunotherapy for recurrent/refractory pediatric medulloblastoma and atypical teratoid rhabdoid tumor
Study
EGAS50000000811
-
Transcriptome changes in circulating immune cells of critical COVID-19 patients predict a specific metabolic and epigenetic imprint
Study
EGAS50000000965
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Fragmentation signatures in cancer patients are similar to those in patients with vascular and autoimmune diseases
Study
EGAS00001008004
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STimage: Robust and interpretable prediction of gene markers and cell types from spatial transcriptomics data
Study
EGAS50000001503
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Adjuvant nivolumab in resected esophageal or gastroesophageal junction cancer: exploratory biomarker analyses from CheckMate 577
Study
EGAS50000001663
-
Monosomy 7 delineates a primitive acute myeloid leukemia with adverse prognosis and responsiveness to epigenetic therapy
Study
EGAS50000001641
-
Kbtbd13 knock-down restores muscle function in a human-based mouse model of nemaline myopathy type 6
Study
EGAS50000001678
-
Full genome sequencing of a monozygotic twin discordant for schizophrenia
Study
EGAS00001000152
-
Cancer genome scanning in plasma: detection of tumor-associated copy number aberrations, single nucleotide variants and tumoral heterogeneity by massively parallel sequencing
Study
EGAS00001000370
-
GEenetic landscape of hypodiploid acute lymphoblastic leukemia
Study
EGAS00001000380
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EuCANCan: EUropean-CANadian Cancer network
Blog
eucancan
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Somatic mutations in ALS genes in the motor cortex of sporadic ALS patients
Study
EGAS00001008104
-
The genomic landscape of relapsed infant and childhood KMT2A-rearranged acute leukemia
Study
EGAS00001008197
-
EATL-II STUDY
Study
EGAS00001001879
-
Inactivation of TGFβ receptors in stem cells drives cutaneous squamous cell carcinoma - 30 whole exomes
Study
EGAS00001001892
-
Transcriptional and functional profiling defines human small intestinal macrophage subsets
Study
EGAS00001002093
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Whole genome sequencing data for 10 hepatocellular carcinomas (HCC) and matched non-tumor liver tissues + optical mapping data for 4 HCC and 3 matched non-tumor liver tissues.
Study
EGAS00001005629
-
Resequencing_candidate_genes_for_male_spermatogenic_impairment
Study
EGAS00001002157
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Genetic Basis of Hepatosplenic T Cell Lymphoma (HSTL)
Study
EGAS00001002182
-
miR-200-regulated CXCL12β promotes fibroblast heterogeneity and immunosuppression in ovarian cancers
Study
EGAS00001002184
-
DONSON encodes a novel replication fork protection factor mutated in microcephalic dwarfism.
Study
EGAS00001002224
-
Whole-Genome Sequencing of a Healthy Aging Cohort.
Study
EGAS00001002306
-
Molecular Subtype-specific Biomarkers Improves Colorectal Cancer Prognostication
Study
EGAS00001002376
-
Orthotopic Patient-Derived Xenografts of Pediatric Solid Tumors
Study
EGAS00001002528
-
Uterine_Atlas_Endometriosis
Study
EGAS00001004725
-
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_WGS
Study
EGAS00001002857
-
Human islet 3D chromatin maps provide insights into type 2 diabetes
Study
EGAS00001002917
-
A comprehensive human gastric cancer organoid biobank captures tumor subtype heterogeneity and enables therapeutic screening
Study
EGAS00001003145
-
Single_cell_analysis_T_cell_activation
Study
EGAS00001003479
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___WG__Novaseq_
Study
EGAS00001003524
-
MutWP5__CRUK_Mutographs_of_Cancer__BRCA_Carriers___Exome__Novaseq_
Study
EGAS00001003526
-
Control iPSC lines with clinically annotated genetic variants for versatile multi-lineage differentiation
Study
EGAS00001003684
-
Single cell transcriptomic analysis of the immune cell compartment in the human small intestine and in Celiac disease
Study
EGAS00001003751
-
Patient-Derived Lung Cancer Organoid
Study
EGAS00001003786
-
Early evolutionary branching across spatial domains predisposes to clonal replacement under chemotherapy in neuroblastoma
Study
EGAS00001007650
-
Establishment and characterization of circulating tumor cells-derived organoids from metastatic breast cancer patients.
Study
EGAS00001007582
-
Lenalidomide Resistance in del(5q) Myelodysplastic Syndrome Follows Loss of RUNX1/TP53-mediated Megakaryocytic Differentiation
Study
EGAS00001004113
-
Dual targeting of polyamine synthesis and uptake in diffuse intrinsic pontine gliomas
Study
EGAS00001004905
-
Adult granulosa cell tumor WGS data cohort with corresponding reference germline WGS data
Study
EGAS00001004249
-
Whole genome sequencing of patients with or at risk for HCC
Study
EGAS00001007249
-
Myelodysplastic cells in patients re-program mesenchymal stromal cells to establish a transplantable stem cell-niche disease unit.
Study
EGAS00001000716
-
Whole exome sequencing for gallbladder cancer in Xinhua Hospital Affiliated to Shanghai Jiao Tong University, School of Medicine
Study
EGAS00001000853
-
ChIP-seq of plasma cell-free nucleosomes identifies gene expression programs of the cells-of-origin
Study
EGAS00001004913
-
Whole_genome_sequencing_in_a_multiplex_Crohn_s_disease_family
Study
EGAS00001000060
-
single cell sequencing of resting and Influenza-stimulated mononcluear phagocytes of African and Europeans with varying degree of ex-vivo susceptibility to Influenza
Study
EGAS00001005000
-
Engineering large chromosomal deletions by CRISPR-Cas9
Study
EGAS00001005134
-
Repli-seq data for 'Replication timing alterations are associated with mutation acquisition during tumour evolution in breast and lung cancer'
Study
EGAS00001007773
-
Mutational Mechanisms in Multiply Relapsed Pediatric Acute Lymphoblastic Leukemia
Study
EGAS00001007900
-
Mapping the human hematopoietic stem and progenitor cell hierarchy through integrated single-cell proteomics and transcriptomics
Study
EGAS00001007930
-
Novel paediatric case of a spinal high-grade astrocytoma with piloid features in a patient with Noonan Syndrome
Study
EGAS00001007937
-
Immune-awakening revealed by peripheral T cell dynamics after one cycle of immunotherapy
Study
EGAS00001004043
-
Differential expression profile of gluten-specific T cells identified by single-cell RNA-seq
Study
EGAS00001005517
-
Serial assessment of measurable residual disease in medulloblastoma liquid biopsies
Study
EGAS00001005592
-
Human induced pluripotent stem cells display a similar mutation burden as embryonic pluripotent cells in vivo
Study
EGAS00001005939
-
Transcriptome analysis in very preterm infants with chronic lung disease after birth
Study
EGAS00001002586
-
The chromatin accessibility signature of human immune aging stems from CD8+ T cells
Study
EGAS00001002605
-
Genetic landscape of Early T-cell precursor acute lymphoblastic leukaemia
Study
EGAS00001000348
-
Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
Study
EGAS00001000443
-
Whole-exome ultra-high throughput sequencing in brain samples of suicide victims who had suffered from major depressive disorder and control subjects who had died from other causes
Study
EGAS00001002818
-
APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UG2G component)
Study
EGAS00001000545
-
Neuroblastoma heterogeneity
Study
EGAS00001007016
-
Single-cell RNA-seq of cervix and placenta
Study
EGAS00001007044
-
Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies
Study
EGAS00001000274
-
Gain of function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions
Study
EGAS00001003231
-
Chordoma_Sequencing_Project_Whole_Genome
Study
EGAS00001000409
-
MGA-NUTM1 fusion in high grade spindle cell sarcoma
Study
EGAS00001003341
-
Transcriptomic classes of BCR-ABL1 lymphoblastic leukemia
Study
EGAS00001007167
-
Single molecule genome-wide mutation profiles of cell-free DNA for non-invasive detection of cancer
Study
EGAS00001007248
-
CD74-NRG1 fusions in lung adenocarcinoma
Study
EGAS00001000653
-
Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
-
White blood cell and cell-free DNA analyses for detection of residual disease in gastric cancer
Study
EGAS00001004114
-
Inferring expressed genes by whole-genome sequencing of plasma DNA
Study
EGAS00001001754
-
Whole genome sequencing of six ethnic groups from Burkina Faso, Cameroon, and Tanzania
Study
EGAS00001003648
-
Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
Study
EGAS00001000941
-
Tracking the origins and drivers of subclonal metastatic expansion in prostate cancer
Study
EGAS00001000942
-
Origins and functional consequence of somatic mitochondrial DNA mutations
Study
EGAS00001000968
-
Frequent alterations in cytoskeleton remodeling genes in primary and metastatic Chinese lung adenocarcinomas
Study
EGAS00001000982
-
Epigenomics and Single-cell Sequencing Define a Developmental Hierarchy in Langerhans Cell Histiocytosis
Study
EGAS00001003822