22938 results for "ega"

in 32.02 milliseconds.

• Cancer-Unknown-Primary-Array-Methylation-H021

  CUP samples using 850k

  Dataset EGAD00010002036

• ChIP_2PEAKS

  Second batch of ChIP-seq narrowPeaks. Software: MACS2 v2.1.2

  Dataset EGAD00010002051

• Greek

  Greek Multiple Sclerosis cases and controls

  Dataset EGAD00010002115

• US

  US Multiple Sclerosis cases and controls

  Dataset EGAD00010002116

• Australia

  Australia Multiple Sclerosis cases and controls

  Dataset EGAD00010002117

• fap_colon

  (A)FAP Colon Crypt - EPIC Methylation Array

  Dataset EGAD00010002198

• endometrium

  Endometrium Gland - EPIC Methylation Array

  Dataset EGAD00010002199

• ProteomicAnalysis(DIA)ofmuscleinvasivebladdercancerpatient-derivedxenografts

  Accesstoproteomicfiles(DIA)ofMIBCpatient-derivedxenografts(N=8)

  Dataset EGAD00010002512

• CNAPs

  Copy Number profiles measured using Affymetrix SNP Array 6.0

  Dataset EGAD00010002544

• DNA_methylation_pancreas

  DNA methylation of PDAC prescursors and normal pancreas cell population

  Dataset EGAD00010002386

• Methylation_gDNA_wbc

  Genome-wide CpG methylation information of genomic DNA samples from white blood cells

  Dataset EGAD00010002586

• HumanCytoSNP12-2-1

  HumanCytoSNP-12 v2.1 on tissue DNA

  Dataset EGAD00010002091

• Phenotypes_CaseFamilies

  Phenotypes from case families listed in medical records and used in analyses.

  Dataset EGAD00010002125

• covarites

  covarites phenotypes, including gender (1=Female/0=Male), age and contraceptive

  Dataset EGAD00010002147

• WGS of 14 paired hepatocellular carcinomas

  Dataset EGAD00001000749

• Methylation_cfDNA_control

  Genome-wide CpG methylation information of cell-free DNA samples from healthy controls

  Dataset EGAD00010002585

• HNF1A haploinsufficiency causes decreased insulin expression, dysregulation of pancreatic progenitor signature genes and affects chromatin accessibility

  Study EGAS00001006309

• Bulk RNA-seq

  Bulk RNA-seq

  Dataset EGAD50000000135

• Swedish schizophrenia study (S3) data access

  Dac EGAC00001003466

• Data Access Committee for the MAXOMOD Consortium - E-Rare / European Joint Programme on Rare Diseases

  Dac EGAC00001003287

• DAC - Dept. of Pathology LUMC

  DAC of the Department of Pathology of Leiden University Medical Center

  Dac EGAC50000000376

• GSA_2020_hg38

  Genopyting of 65 individuals using the Illumina Global Screening Array-24 v2

  Dataset EGAD00010002706

• GSA_2023_hg19

  Genopyting of 45 individuals using the Illumina Global Screening Array-24 v3

  Dataset EGAD00010002707

• GSA_2022_hg19

  Genopyting of 45 individuals using the Illumina Global Screening Array-24 v3

  Dataset EGAD00010002705

• 5' Single cell RNA sequencing of pre-treatment tissues from lung cancer patients receiving immunotherapy

  Study EGAS00001006188

• The landscape of somatic mutations in epigenetic regulators across 1000 pediatric cancer genomes

  Study EGAS00001000449

• The Cardiogenics study

  Study EGAS00001000411

• Identification of mutations and structural rearrangements in plasma DNA form metastatic prostate cancer patients

  Study EGAS00001000453

• Expression profiles and genetic makeup of metastases of a cancer of unknown primary.

  Study EGAS00001004059

• Fresh vs. frozen cell preparations of colorectal cancer single-cell RNA sequencing

  Study EGAS00001003769

• Single cell sequencing: Capturing the origin and dynamics of chromosomal copy-number heterogeneity

  Study EGAS00001003812

• Concurrent germline and somatic pathogenic BAP1 variants in a patient with metastatic bladder cancer

  Study EGAS00001004055

• STM4 - Mouliere et al, 2018. Enhanced detection of circulating tumor DNA by fragment size analysis

  Study EGAS00001004418

• Human gastrointestinal epithelia of the esophagus, stomach and duodenum resolved at single-cell resolution

  Study EGAS00001004695

• Characterization of stromal tumor-infiltrating lymphocytes and genomic alterations in metastatic lobular breast cancer

  Study EGAS00001004641

• BRCA2, ATM, and CDK12 defects differentially shape prostate tumor driver genomics and clinical aggression

  Study EGAS00001004800

• IG-MYC rearrangement defines a high-risk subgroup of B-cell precursor acute lymphoblastic leukaemia

  Study EGAS00001005111

• Genomic Analysis of Focal Nodular Hyperplasia with Associated Hepatocellular Carcinoma Unveils its Malignant Potential

  Study EGAS00001005313

• Immune infiltrate and tumor microenvironment transcriptional programs stratify pediatric osteosarcoma into prognostic groups at diagnosis

  Study EGAS00001005326

• Evaluating CRISPR-based Prime Editing for cancer modeling and CFTR repair in organoids

  Study EGAS00001005358

• Orthotopic murine Group 3 medulloblastoma in C57Bl/6 mice treated with saline, cyclophosphamide or gemcitabine

  Study EGAS00001005846

• Orthotopic murine Group 3 medulloblastoma in C57Bl/6 mice treated with sham or craniospinal irradiation

  Study EGAS00001005847

• Integrated single-cell profiling dissects cell-state-specific enhancer landscapes of human tumor infiltrating T cells.

  Study EGAS00001006141

• Genomic profiling of metastatic basal cell carcinoma reveals candidate drivers of disease and therapeutic targets

  Study EGAS00001006148

• Neutrophil extracellular traps have auto-catabolic activity and produce mononucleosome-associated circulating DNA

  Study EGAS00001006759

• NPY methylated ctDNA is a promising biomarker for treatment response monitoring in metastatic colorectal cancer

  Study EGAS00001006820

• JAK/STAT signaling promotes the emergence of regenerative cell states in ulcerative colitis

  Study EGAS00001007098

• Transcriptome analyses of a large cohort of adult B cell acute lymphoblastic leukemia samples

  Study EGAS00001007217

• Mechanism of action and resistance to Trastuzumab Deruxtecan in patients with metastatic breast cancer

  Study EGAS00001007372

• CUPiD, a cfDNA methylation-based tissue-of-origin classifier for Cancers of Unknown Primary

  Study EGAS00001007445

• RAGE engagement by SARS-CoV-2 enables monocyte infection and underlies COVID-19 severity

  Study EGAS00001007529

• Low-coverage whole-genome sequencing of cancer and healthy plasma circulating DNA

  Study EGAS00001007593

• scRNA-seq analysis Identifies Hepatic IL-13-Producing ILC3-Like Cells Potentially Linked to Liver Fibrosis

  Study EGAS00001007207

• The WID-EC test for the detection and risk prediction of endometrial cancer

  Study EGAS00001005033

• The DNA methylome of cervical cells and risk of ovarian cancer

  Study EGAS00001005045

• Genomic profiling of subcutaneous patient derived xenograft models of solid childhood cancer

  Study EGAS00001006710

• LUFR_FGFR2_DAC

  DAC to have access to "Resistance to selective FGFR2 inhibitors across FGFR2-driven malignancies" data

  Dac EGAC50000000212

• DEREGULATION OF PRE-mRNA SPLICING IN MISMATCH REPAIR DEFICIENT COLORECTAL CANCER

  Study EGAS00001004863

• Medulloblastoma WES

  WES for tumor and normal samples

  Study EGAS50000000261

• Single Cell Transcriptomics of peripheral immune cells pre- and post-Immune Checkpoint Blockade

  Study EGAS00001005507

• Characterization of UV DNA damage in B-cell precursor acute lymphoblastic leukemia

  Study EGAS00001008128

• The data access committee for "Validation of cfDNA fragmentome analyses for early detection of liver cancer"

  Dac EGAC00001003543

• An Integrated Approach to Patient Stratification and Therapy Selection in Acute Myeloid Leukemia

  Study EGAS00001004655

• Human oligodendroglial progenitor cells (hGPCs/OPCs) derived from induced pluripotent stem cell (iPS) scCRISPRi/a-seq

  Dac EGAC50000000804

• Single cell RNA sequencing of relapsed/refractory multiple myeloma

  Study EGAS00001004805

• LIONESS DAC

  This DAC will govern access to WES data associated with the LIONESS study.

  Dac EGAC50000000613

• Whole Genome Methylation in CLL

  Study EGAS00001000272

• WGS of oesophagogastric cancer

  WGS of 12 oesophagogastric cancer samples WGS or 12 matched germline data.

  Dac EGAC50000000890

• Genetic landscape of non-Down syndrome acute megkaryoblastic leukemia

  Study EGAS00001000379

• GEenetic landscape of hypodiploid acute lymphoblastic leukemia

  Study EGAS00001000380

• A renal cell carcinoma tumorgraft platform to advance precision medicine

  Study EGAS00001005516

• Subgroup-specific gene expression profiles and mixed epistasis in chronic lymphocytic leukemia (HIPO, H005)

  Study EGAS00001006361

• SF4209

  RNA-exome

  Dataset EGAD00001006768

• Angiosarcoma_whole_exome

  Extension of angiosarcoma whole genome sequencing study

  Study EGAS00001000588

• Angiosarcoma_RNA_sequencing

  Extension of angiosarcoma whole genome sequencing study

  Study EGAS00001000590

• FFPE_whole_genome_pilot

  To assess feasibility of whole genome sequencing

  Study EGAS00001001967

• Angiosarcoma_targeted_pulldown_cancer_gene_panel

  Extension of angiosarcoma whole genome sequencing study

  Study EGAS00001000589

• Deep_sequencing_of_melanoma_for_driver_mutations

  Deep sequencing of melanoma for driver mutations

  Study EGAS00001000857

• SF6953

  RNA-exome

  Dataset EGAD00001006750

• SF9259

  RNA-exome

  Dataset EGAD00001006751

• SF11248

  RNA-exome

  Dataset EGAD00001006752

• PCGP ERG (WXS)

  DATA FILES FOR PCGP SJERG (WXS)

  Dataset EGAD00001002677

• SF6996

  RNA-exome

  Dataset EGAD00001006760

• SF9135

  RNA-exome

  Dataset EGAD00001006747

• PCGP ERG (WGS)

  DATA FILES FOR PCGP SJERG (WGS)

  Dataset EGAD00001002676

• SF10750

  RNA-exome

  Dataset EGAD00001006748

• SF12165

  RNA-exome

  Dataset EGAD00001006745

• SF10931

  RNA-exome

  Dataset EGAD00001006765

• SF8963

  RNA-exome

  Dataset EGAD00001006764

• SF4324

  RNA-exome

  Dataset EGAD00001006766

• Exome sequencing of 102 French-Canadians

  Exome sequencing of 102 French-Canadians

  Dataset EGAD00001002890

• Noninvasive Prenatal Molecular Karyotyping from Maternal Plasma

  Noninvasive Prenatal Molecular Karyotyping from Maternal Plasma

  Dataset EGAD00001000395

• SF6136

  RNA-exome

  Dataset EGAD00001006754

• SE6136

  RNA-exome

  Dataset EGAD00001006833

• SE4987

  RNA-exome

  Dataset EGAD00001006835

• Angiosarcoma targeted pulldown cancer gene panel

  Extension of angiosarcoma whole genome sequencing study

  Dataset EGAD00001001064

• SF11780

  RNA-exome

  Dataset EGAD00001006757

• SF11094

  RNA-exome

  Dataset EGAD00001006755

• SF10770

  RNA-exome

  Dataset EGAD00001006761

• SF7196

  RNA-exome

  Dataset EGAD00001006762

• SF11215

  RNA-exome

  Dataset EGAD00001006763

• SF8642

  RNA-exome

  Dataset EGAD00001006749

• SF12243

  RNA-exome

  Dataset EGAD00001006758

• SF9490

  RNA-exome

  Dataset EGAD00001006753

• SF9301

  RNA-exome

  Dataset EGAD00001006759

• SF6839

  RNA-exome

  Dataset EGAD00001006769

• SF11587

  RNA-exome

  Dataset EGAD00001006770

• SF9640

  RNA-exome

  Dataset EGAD00001006771

• SF6587

  RNA-exome

  Dataset EGAD00001006772

• 20200819_EGA_Qld_Melanoma.biomarkers

  A study looking at Germline and Somatic biomarkers using WES data only

  Dataset EGAD00001006374

• SE10497

  RNA-exome

  Dataset EGAD00001006834

• SF10228

  RNA-exome

  Dataset EGAD00001006756

• SE4831

  RNA-exome

  Dataset EGAD00001006830

• Cancer Alliance WGS

  Whole genome sequencing for individualized cancer interpretation

  Dataset EGAD00001006233

• SE9037

  RNA-exome

  Dataset EGAD00001006832

• SF10064

  RNA exome

  Dataset EGAD00001006744

• SF10127

  RNA-exome

  Dataset EGAD00001006767

• RNA-seq

  RNA-seq of PDXs

  Dataset EGAD00001001862

• TRAIP patients

  BAM files for two WES TRAIP patients

  Dataset EGAD00001001633

• Sequencing of rare human histiocytic tumour

  Sequencing of rare human histiocytic tumour

  Dataset EGAD00001002184

• CB

  CB: Aligned sequences used in the error modeling study

  Dataset EGAD00001005261