23249 results for "ega"

in 26.43 milliseconds.

• Global Anaplastic Thyroid Cancer Initiative

  Raw exome sequence data(fastq) for the GATCI project

  Dataset EGAD00001003235

• Somatic mutations in angiosarcoma

  Here we present the genomes of three secondary angiosarcomas

  Dataset EGAD00001000735

• HCA Organoids | Colon - Cancer, WES

  HCA Organoids | Colon - Cancer, Whole Exome Sequencing (WES)

  Dataset EGAD00001015548

• AML WGS bam

  WGS bam files for paired diagnostic and remission samples

  Dataset EGAD00001015515

• The data access committee for Single molecule genome-wide mutation profiles of cell-free DNA for non-invasive detection of cancer

  Dac EGAC00001003253

• The Nordic Centre of Excellence Programme in Molecular Medicine Data Access Committee

  Dac EGAC00000000006

• Data access agreement for ATRT

  Dac EGAC00001000306

• Tumor Genomics Committee - EGAC00001000987

  Dac EGAC00001000987

• Data Access Commitee for Schulte-Schrepping et al., 2020: Severe COVID-19 is marked by a dysregulated myeloid cell compartment

  Dac EGAC00001001684

• Chair of Experimental Medicine and Therapy Research Regensburg DAC

  Dac EGAC00001001699

• Commitee of Evolution of PDAC, Department of Bilary-Pancreatic Surgery, Shanghai Renji Hospital, School of Medicine, Shanghai Jiao Tong University

  Dac EGAC00001001823

• Expression-Based Subtypes Define Pathologic Response to Neoadjuvant Immune-Checkpoint Inhibitors in Muscle-Invasive Bladder Cancer

  Dac EGAC00001002276

• EGAD00000000026

  Randomly-selected, unrelated individuals

  Dataset EGAD00000000026

• EGAD00010000690

  Genome-wide SNP genotyping of African rainforest hunter-gatherers and neighbouring agriculturalists by Illumina HumanOmniExpress

  Dataset EGAD00010000690

• EGAD00010000724

  Pilot experiment on functional genomics in osteoarthritis (methyl)

  Dataset EGAD00010000724

• EGAD00010000278

  SCLC matched normal genotypes

  Dataset EGAD00010000278

• EGAD00010000391

  Cambridge control samples using a 660K genotyping chip from Illumina

  Dataset EGAD00010000391

• EGAD00010000474

  blood-based gene expression from breast cancer cases and age-matched controls in case-control serie 2 (CC2)

  Dataset EGAD00010000474

• EGAD00010000476

  blood-based gene expression from breast cancer cases and age-matched controls in case-control serie 1 (CC1)

  Dataset EGAD00010000476

• EGAD00010000478

  blood-based gene expression from breast cancer cases and age-matched controls in case-control serie 3 (CC3)

  Dataset EGAD00010000478

• EGAD00010000480

  ccRCC case samples using 250K Nsp

  Dataset EGAD00010000480

• EGAD00010000498

  Affymetrix SNP6.0 genotype data for prostate cancer patients

  Dataset EGAD00010000498

• EGAD00010000506

  WTCCC2 BO (Barretts oesophagus) samples

  Dataset EGAD00010000506

• EGAD00010000518

  Samples from the Greek island of Crete, MANOLIS cohort

  Dataset EGAD00010000518

• EGAD00010000536

  21 unlinked autosomal microsatellite loci for 30 Central Asian populations

  Dataset EGAD00010000536

• Exome sequencing of hyperplastic polyposis patients.

  Exome sequencing of hyperplastic polyposis patients.

  Dataset EGAD00001000015

• Lethal malformation syndrome

  Lethal malformation syndrome

  Dataset EGAD00001000019

• Screening for human epigenetic variation at CpG islands

  Screening for human epigenetic variation at CpG islands

  Dataset EGAD00001000059

• Mixed Leukemia Rearrangement Screen

  Mixed Leukemia Rearrangement Screen

  Dataset EGAD00001000065

• CRLF2 sequencing project Exomes

  CRLF2 sequencing project Exomes

  Dataset EGAD00001000077

• Matched Ovarian Cancer Sequencing

  Matched Ovarian Cancer Sequencing

  Dataset EGAD00001000084

• ER-, HER2-, PR- breast Cancer genome sequencing

  ER-, HER2-, PR- breast Cancer genome sequencing

  Dataset EGAD00001000088

• Breast Cancer Exome Resequencing

  Breast Cancer Exome Resequencing

  Dataset EGAD00001000093

• Cancer Genome Libraries Tests

  Cancer Genome Libraries Tests

  Dataset EGAD00001000094

• Polycythemia Vera Myeloproliferative Disease exome sequencing

  Polycythemia Vera Myeloproliferative Disease exome sequencing

  Dataset EGAD00001000123

• Triple Negative Breast Cancer Whole Genomes

  Triple Negative Breast Cancer Whole Genomes

  Dataset EGAD00001000141

• UK10K_OBESITY_SCOOP REL-2012-01-13

  UK10K_OBESITY_SCOOP REL-2012-01-13

  Dataset EGAD00001000181

• DATA FILES FOR SJACT (WGS)

  DATA FILES FOR SJACT

  Dataset EGAD00001000160

• DATA FILES FOR SJINF

  DATA FILES FOR SJINF

  Dataset EGAD00001000165

• Functional characterisation of CpG islands in human tissues

  Functional characterisation of CpG islands in human tissues

  Dataset EGAD00001000212

• Melanoma-TIL Study Exomes

  Melanoma-TIL Study Exomes

  Dataset EGAD00001000243

• Fastq files for SAIF genome

  This dataset contain the raw files generated for SAIF genome project

  Dataset EGAD00001000254

• Variant_files_100_ID_trios

  High Quality Variant Call files, generated by bioscope, converted to vcf format. Complete dataset for all 300 samples.

  Dataset EGAD00001000277

• The UCSF Low Grade Glioma Genome Project #1

  Dataset EGAD00001000714

• RNAseq of PC-9 and KHM-3S with and without tarceva

  Dataset EGAD00001000843

• Whole Exome Sequencing for Verhaak-GBM

  Dataset EGAD00001001111

• Ewing sarcoma genome sequencing

  Dataset EGAD00001001051

• DATA FILES FOR BALL-PAX5-WES

  Dataset EGAD00001001056

• Whole Exome Data for Verhaak-GBM

  Dataset EGAD00001001112

• Whole Exome sequencing for Verhaak-GBM

  Dataset EGAD00001001113

• Methylation differences in trisomy 21 using monozygotic twins - RRBS dataset

  Dataset EGAD00001001272

• DNA_Methylation_450K

  BLUEPRINT DNA methylation profiles of monocytes, neutrophils and T cells from healthy donors

  Dataset EGAD00010000850

• lnFXI_metaanalysis_summarydata

  Summary data from Meta-analysis of Genome-Wide-Association Studies for plasma levels of Coagulation Factor XI (FXI)

  Dataset EGAD00010001141

• OCAC OncoArray data

  Germline genotype data on 56,479 ovarian cancer cases and controls

  Dataset EGAD00010001192

• Melanoma_SNP6

  Melanoma cell lines CNV by SNP6

  Dataset EGAD00010001216

• 450K_DKFZ_ACC_CJ

  primary human ACC and normal samples using 450K

  Dataset EGAD00010001298

• Medulloblastoma expression profiling (mbt)

  Medulloblastoma expression profiling

  Dataset EGAD00010001300

• NSAID-LIV

  1000G Phase 3 Imputed cases and controls from NSAID-induced PUD study

  Dataset EGAD00010001422

• HGP-U-1

  Himalayan population genetic study raw data (Himalaya)

  Dataset EGAD00010001472

• Thai Cases

  252 dengue fever patients and 159 dengue shock syndrome patients

  Dataset EGAD00010001487

• SNP array datas of Matched cancer-PNE

  SNP array datas of Matched cancer-PNE

  Dataset EGAD00010001631

• Identification of molecular subgroups in multiple myeloma by whole exome sequencing.

  Dataset EGAD00001004408

• Transcriptome sequencing of Gingivo-buccal Cancer : ICGC-India Project_Batch05

  Dataset EGAD00001004430

• RHD_NC_OMNI_Cases

  Rheumatic heart disease cases recruited in New Caledonia with higher density genotyping

  Dataset EGAD00010000956

• WhereAreYouFrom 517K

  Where Are You From? samples types at 517K SNP loci

  Dataset EGAD00010000952

• Blood dataset - Case

  blood-based gene expression from breast cancer cases

  Dataset EGAD00010001063

• EXCEED Study HRC imputation

  EXCEED samples imputed to HRC reference panel using Michigan Imputation server

  Dataset EGAD00010001685

• 1506_Methylation_M.vd.Berge

  DNA methylation in bronchial biopsies of asthmatics, asthma in remission and healthy subjects

  Dataset EGAD00010001731

• nenets

  Genotypes of nenets people from Yamalo-Nenets Autonomous Okrug (Russia)

  Dataset EGAD00010001776

• EPIC

  EPIC array data from 72 tumor samples with muscle invasive bladder cancer.

  Dataset EGAD00010001921

• methylation_normal_breast

  Raw methylation data from normal breast tissue.

  Dataset EGAD00010002076

• SAFIR02_Agilent

  Genomics to select patients with metastatic breast cancer for targeted therapy (microarray_agilent)

  Dataset EGAD00010002243

• PBMC_genotypes

  Combined genotyping files from 13 PBMC samples

  Dataset EGAD00010002308

• Immune Checkpoint Associated Acute Interstitial Nephritis

  Tertiary lymphoid structure signatures are associated with immune checkpoint inhibitor related acute interstitial nephritis

  Dataset EGAD00010002406

• hyper_hypo_methylation_proportion_Roadmap

  Proportion of hyper- and hypomethylated positions at Roadmap annotations. Data from 8 individuals.

  Dataset EGAD00010002416

• AS_genotyping

  AS genotyping data for lead SNPs using Illuminia Global Array V2.0

  Dataset EGAD00010002476

• Amplicon 16SrRNA-V4-stool Leuven CRC Progression Microbiome cohort (LCPM)

  Amplicon sequencing

  Dataset EGAD50000000267

• DAC for the study molecular biomarkers associated with the diagnosis and severity of genetic and diseases from PAIDI-BIO354 GENYO-UGR)

  Dac EGAC00001003090

• WES for cell lines UWB1.289 and COV362

  exon 11 mutated UWB1.289 and COV362 cell lines

  Dataset EGAD50000000189

• DAC for BCP-LBL Kiel

  Whole exome sequencing and RNA sequencing of B-Cell Precursor Lymphoblastic Lymphoma tissue biopsies.

  Dac EGAC50000000181

• Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Germany

  Study EGAS00001005858

• DupiAERD DAC

  DAC to regulate access to RNA sequencing data of NERD patients with dupilumab treatment before and after aspirin provocation.

  Dac EGAC50000000273

• resistance to FGFR inhibitor from RNA sequencing

  WTS performed on tissues from resistant patients

  Study EGAS50000000306

• targeted DNA sequencing data

  a total number of 203 targeted DNA sequencing lymphoma samples

  Dataset EGAD50000000632

• Schirmer Lab

  Medizinische Fakultät Mannheim der Universität Heidelberg, Theodor-Kutzer-Ufer 1 - 3, 68167, Mannheim, Baden-Württemberg, Germany

  Dac EGAC50000000231

• Engineering Immune Cells for Therapy, Institute for Medical Microbiology, Immunology and Hygiene, Technical University Munich

  CRISPR engineering of human T cells

  Dac EGAC50000000405

• Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features

  Study EGAS00001005346

• Somatic mutations in healthy and leukemic blood progenitors reveal evolutionary mechanisms underlying childhood leukemia and differential patient outcome

  Study EGAS00001004593

• Gene expression profiles of disseminated breast cancer cells

  Study EGAS00001004597

• Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients

  Study EGAS00001004975

• Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features

  Study EGAS00001005355

• RNA-seq on neuroblastoma PDX model COG-N-519 treated with control miR-1283 and test miR-99b-5p mimics

  Study EGAS00001005368

• Whole transcriptome profiling of liquid biopsies from tumour xenografted mouse models enables specific monitoring of tumour-derived extracellular RNA

  Study EGAS00001005740

• Single-cell multi-omics of human clonal hematopoiesis reveals that DNMT3A R882 mutations perturb early progenitor states through selective hypomethylation.

  Study EGAS00001006364

• transcriptome analysis of NK cells sorted from PBMCs at baseline and after addition of a T cell dependent bispecific antibody (TDB)

  Study EGAS00001006914

• The effector program of human CD8 T cells can promote both target cell killing and tissue remodeling

  Study EGAS00001006960

• RNA sequencing of in vitro generated suppressive myeloid cells using parental and Sialidase expressing A549 cancer cell lines

  Study EGAS00001007618

• DAC for study involving the spatial transcriptomics analysis of HPV-dependent and HPV-independent vulval squamous cell carcinoma at Imperial College London.

  Dac EGAC00001003515

• PEVOsq WES data

  Raw paired FASTQ data of patients at baseline from the PEVOsq cohort

  Dataset EGAD50000001013

• Structural and Non-Coding Variants Increase the Diagnostic Yield of Clinical Whole Genome Sequencing for Rare Diseases

  Study EGAS00001007575