22938 results for "ega"

in 96.40 milliseconds.

• microRNA

  Breast cancer tissue and controls

  Dataset EGAD00010001406

• RHD_NC_HC24_Cases

  Rheumatic heart disease cases recruited in New Caledonia

  Dataset EGAD00010000957

• Southeast_Borneo_730K

  Genotyping data from Southeast Borneo individuals

  Dataset EGAD00010000944

• dataset1

  BLUEPRINT DNA Methylation 450K data of mantle cell lymphoma

  Dataset EGAD00010001012

• HMEC Non-label-retaining cells

  Gene expression after mammosphere culture, non-label-retaining cells

  Dataset EGAD00010001966

• MCF10A 24h IL6 trans-signaling

  Gene expression after cell culture, 24h Hyper-IL6 stimulated

  Dataset EGAD00010001969

• A3164_ClariomD

  ALL SAMPLES USING ClariomD microarray (Affymetrix)

  Dataset EGAD00010001705

• native_american_pops_Axiom_Human_Origins

  Sample genotyped with Axiom Human Origins (Affymetrix)

  Dataset EGAD00010001803

• tupiniquim_guarani_Axiom_InCor_BB

  Sample genotyped with Axiom InCor BB (Affymetrix)

  Dataset EGAD00010001802

• MCF10A 12h IL6 trans-signaling

  Gene expression after cell culture, 12h Hyper-IL6 stimulated

  Dataset EGAD00010001960

• Hydroxycarbamide effect on DNA methylation_CD34

  DNA methylation measures on CD34 cells

  Dataset EGAD00010001941

• Finland-Immuno

  Finland Multiple Sclerosis case

  Dataset EGAD00010002048

• colon

  Normal Colon Crypt - EPIC Methylation Array

  Dataset EGAD00010002200

• Genotype_controls

  PLINK file of Japanese controls

  Dataset EGAD00010002340

• PDAC-Microarray-Clariom-S-data

  Microarray data of 14 patient-derived PDAC cultures

  Dataset EGAD00010002443

• FRONTIER DNA methylation

  Tumor biopsies profiled by DNA methylation array

  Dataset EGAD00010002182

• Aboriginal Genetics and Health Studies based at the Telethon Kids Institute, Perth, Western Australia

  Dac EGAC00001000261

• Methylation_WB_RA

  Peripheral blood DNA methylome in adalimumab-treated patients with rheumatoid arthritis

  Dataset EGAD00010002610

• INCLIVA-CC-panel DAC

  Colon cancer targeted sequencing study contaning WBCs, primary tumor tissue and plasma samples

  Dac EGAC50000000061

• Idiopathic Collapsing Glomerulopathy - Brazil

  Database of Whole Exome Sequencing of brazilian patients diagnosed with Idiopathic Collapsing Glomerulopathy

  Dac EGAC50000000012

• This DAC takes care of requests for data for the Swiss epigenetic colorectal cancer cohort study, SWEPIC

  Dac EGAC00001003471

• Ultra-deep targeted sequencing for studying the accumulation of somatic mutations in cancer-free human skin

  Study EGAS00001004279

• A population specific reference genome defined from the analysis of 153 United Arab Emirates nationals.

  Study EGAS00001004537

• Transcriptome Analysis Offers a Comprehensive Illustration of the Genetic Background of Pediatric Acute Myeloid Leukemia

  Study EGAS00001003701

• Healthy_pleura

  EPIC methylation data of pleural mesothelioma samples and healthy pleura samples

  Dataset EGAD00010002656

• Pleural_mesothelioma

  EPIC methylation data of pleural mesothelioma samples and healthy pleura samples

  Dataset EGAD00010002657

• Buccal sample methylation from breast cancer cases

  Buccal sample methylation from breast cancer cases

  Dataset EGAD00010002635

• Methylation_cfDNA_cancer

  Genome-wide CpG methylation information of cell-free DNA samples from cancer patients

  Dataset EGAD00010002587

• Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia

  Study EGAS00001006878

• Illumina MethylationEPIC Repeatability dataset

  Raw methylation data from technical replicates processed on EPIC v1.0.

  Dataset EGAD00010002501

• NanoString Panel Standard

  RCC files of 17 Cartridges' Panel Standards

  Dataset EGAD00010002431

• NanoString Cancer

  RCC files of 17 Cartridges from metastatic melanoma

  Dataset EGAD00010002432

• GWAS data of the AlpeDPD study

  GWAS data of the AlpeDPD trail cohort

  Dataset EGAD00010002684

• Dataset for the spanish node

  Dataset for the spanish node

  Dataset EGAD50000000884

• DAC Department of Neurology, TUM University Hospital, Technical University of Munich, School of Medicine and Health

  Dac EGAC00001003508

• Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma

  Study EGAS00001000226

• PBAT sequencing of cytotrophoblast and mural trophectoderm

  PBAT sequencing of primary first trimester cytotrophoblast and mural trophectoderm

  Dac EGAC50000000424

• Preliminary Results from the Initiative for Molecular Profiling and Advanced Cancer Therapy 2 (IMPACT 2) Study

  Study EGAS00001004964

• MutationalPatterns2: The one stop shop for the analysis of mutational processes: DNA repair deletions

  Study EGAS00001004789

• Hepatocellular carcinoma xenografts established from needle biopsies preserve the characteristics of the originating tumors

  Study EGAS00001003396

• Genomic insight into the origins and dispersal of the Brazilian Coastal Natives

  Study EGAS00001004036

• Quality of Whole Genome Sequencing from Blood versus Saliva Derived DNA in Cardiac Patients

  Study EGAS00001004115

• High coverage sequencing of a single sample can account for the problem of intratumor heterogeneity

  Study EGAS00001004200

• : Centromeric cohesion failure invokes a conserved choreography of chromosomal mis-segregations in pancreatic neuroendocrine tumours

  Study EGAS00001004239

• Multiregion Whole-Exome Sequencing Uncovers the Genetic Evolution and Mutational Heterogeneity of Early-Stage Metastatic Melanoma.

  Study EGAS00001004320

• Candidate Gene Case Control Study of Human African Trypanosomiasis in the Democratic Republic of Congo

  Study EGAS00001004365

• Swarm Learning to identify COVID-19, tuberculosis and leukemia patients based on blood transcriptomes

  Study EGAS00001004502

• Evolutionary trajectories and clonal migration underlying tumor progression and lymph node metastasis in resectable lung cancer

  Study EGAS00001005242

• Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing

  Study EGAS00001005401

• SMARCA4/2 loss inhibits chemotherapy-induced apoptosis by restricting IP3R3-mediated Ca2+ flux to mitochondria

  Study EGAS00001005448