22938 results for "ega"

in 28.52 milliseconds.

• Mutational landscape and clonal architecture in grade-II/III gliomas

  Dataset EGAD00001001213

• GIS-LUNGTCR1-2016_SNP-ARRAY_CASE

  This dataset contains 61 tumors SNP-array dataset from 15 EGFR mutant lung adenocarcinoma patients.

  Dataset EGAD00010001177

• GIS-LUNGTCR1-2016_SNP-ARRAY_CONTROL

  This dataset contains 15 control SNP-array dataset from 15 EGFR mutant lung adenocarcinoma patients.

  Dataset EGAD00010001176

• Codelink_HWG_CLD_B

  Codelink Human Whole Genome from Blood taken at 72 hours after birth (11 cases)

  Dataset EGAD00010001424

• Codelink_HWG_noCLD_CB

  Codelink Human Whole Genome from Blood taken at 72 hours after birth (9 controls)

  Dataset EGAD00010001425

• mRNA profiling of human plucked hair follicle

  mRNA profiling of human plucked hair follicle from frontal and occipital scalp

  Dataset EGAD00010001501

• 5074STDY-G-1

  Genetic Overlap between Metabolic and Psychiatric disease

  Dataset EGAD00010001484

• EXOME_ARRAY_ANALYSIS

  EXOME ARRAY ANALYSIS OF ADVERSE REACTIONS TO FLUOROPYRIMIDINE-BASED THERAPY FOR GASTROINTESTINAL CANCER

  Dataset EGAD00010001499

• EGA_PBC_phased

  A cohort of 2886 participants of the Japan PBC-GWAS Study

  Dataset EGAD00010001533

• Whole Genome Sequencing of Gingivo-buccal Cancer: ICGC-India Project_YR03

  Dataset EGAD00001004478

• C3_PBCR

  WTCCC3_Primary Biliary Cirrhosis Replication

  Dataset EGAD00010000929

• Breast cancer SNP6 arrays_more

  Affymetrix SNP6.0 array breast cancer data

  Dataset EGAD00010001079

• RNA-seq data from 70 non-small cell lung cancer (NSCLC)

  Dataset EGAD00001006145

• WTCCC1_550K

  WTCCC1 project samples from 1958 British Birth Cohort

  Dataset EGAD00010001004

• RNA-Sequencing generated from 180 human putamen and substantia nigra

  Dataset EGAD00001005526

• methylation_tnbc

  Raw methylation data from triple negative breast cancer.

  Dataset EGAD00010002077

• DNA methylation for EGAS00001003603

  Genome-wide DNA methylation profiling of Waldenstrom's macroglobulinemia (WM) patient samples

  Dataset EGAD00010001861

• NativeAmericans_InstitutoNacionaldeSalud_hg38_autosomic_3group

  Genome-wide data for 130 Native American individuals from Peru

  Dataset EGAD00010001992

• NativeAmericans_InstitutoNacionaldeSalud_hg37_autosomic_1group

  Genome-wide data for 71 Native American individuals from Peru

  Dataset EGAD00010001991

• NativeAmericans_InstitutoNacionaldeSalud_hg38_autosomic_2group

  Genome-wide data for 59 Native American individuals from Peru

  Dataset EGAD00010001990

• MethylationEPIC_JMML_tech_Schoenung

  DNA methylation analysis of JMML patients from Europe, Japan and USA using EPIC arrays

  Dataset EGAD00010001998

• MethylationEPIC_JMML_valid_Schoenung

  DNA methylation analysis of JMML patients from Europe, Japan and USA using EPIC arrays

  Dataset EGAD00010002000

• Methylation450k_JMML_meta_Schoenung

  DNA methylation analysis of JMML patients from Europe, Japan and USA using 450k arrays

  Dataset EGAD00010001999

• Array_data_psychosis

  Array data from a family with high prevalence of psychosis

  Dataset EGAD00010002028

• Array_data

  Array data from a family with high prevalence of psychosis

  Dataset EGAD00010002030

• preQC Genotypes

  preQC genotype data from the Affymetrix AxiomTM HGCoV2 1 array in plink ped/map format

  Dataset EGAD00010002437

• BRACOVID_genotype

  Cohort: Raw genotype files for BRACOVID cohort. Genotype Chip: Axiom_PMRA.r3 array genomic build: b37

  Dataset EGAD00010002172

• Genotype_HSM1_HSM2

  Genotypes for 2 human skeletal muscle samples

  Dataset EGAD00010002248

• Methylation

  Illumina EPIC arrays Naevus Melanoma Spitz Case

  Dataset EGAD00010002312

• HI_genotypes

  Human islet samples genotype data

  Dataset EGAD00010002346

• Gentoypes_SouthAfrica

  Individuals genotyped on the Illumina Omni2.5. Autosome and X chromosome.

  Dataset EGAD00010002467

• Panamanian genotype data

  84 Indigenous and admixed individuals from Panama genotyped with Axiom Human Origins (Affymetrix)

  Dataset EGAD00010002473

• Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets

  Dataset EGAD00001001096

• Whole Exome Sequencing of 15 Tumor/Normal pairs of inflammatory hepatocellular adenomas

  Dataset EGAD00001005283

• Institute of Neuropathology - University of Freiburg Medical Center

  The Data Access Committee of the Institute of Neuropathology Freiburg.

  Dac EGAC50000000033

• OICR-DAC, Ontario Institute for Cancer Research

  Dac EGAC00001000591

• OICR-DAC, Ontario Institute for Cancer Research

  Dac EGAC00001000710

• CCA NanoString data (60CCA)

  Raw .RCC files for NanoString. nCounter PanCancer IO 360 Panel was used

  Dataset EGAD00010002612

• Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Dublin, Ireland.

  Study EGAS00001005844

• RNA alignment

  RNAseq aligned to hg38.p14 using nfcore/RNA-seq

  Dataset EGAD50000000428

• Sample Sheet

  Sample sheet for aligning samples with patients.

  Dataset EGAD50000000484

• Azienda Ospedaliero-Universitaria di Parma Data Accessibility

  Regulation on the sharing and accessibility of data belonging to Azienda Ospedaliero-Universitaria di Parma

  Dac EGAC50000000239

• Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Umea, Sweden.

  Study EGAS00001005842

• Lifelines NEXT HMO Data

  The dataset contains HMO measurements for 1542 samples from Lifelines NEXT cohort

  Dataset EGAD50000000531

• Whole Exome Sequencing of Bipolar cases and controls performed at the Broad Institute on a cohort from Cardiff, UK (Craddock)

  Study EGAS00001005845

• Genome-wide array data from Eivissa and Menorca

  DAC for the Genome-wide array data from 22 Eivissan and 20 Menorcan individuals.

  Dac EGAC50000000297

• Metadata associated with sequencing

  Associated metadata for sequencing data.

  Dataset EGAD50000000528

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

  Study EGAS00001005854

• Genetic investigation of 12q-amplified osteosarcomas

  Genetic investigation of 12q-amplified osteosarcomas using both whole genome short- and longread and transcriptome sequencing.

  Dac EGAC50000000340

• Multi-omics analysis of pre-invasive lung adenocarcinoma in never-smokers

  Multi-omics analysis of pre-invasive lung adenocarcinoma in never-smokers

  Dac EGAC50000000385

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

  Study EGAS00001005851

• Comparing sequencing of four proto-typical Burkitt lymphomas (BL) with IG-MYC translocation.

  Study EGAS00001000271

• Whole Exome Sequencing of Spanish Patients diagnosed with rare ophtalmogenetic disorders: Macular Dystrophy, Retinitis Pigmentosa and Leber's congenital amaurosis.

  Study EGAS00001004084

• Integration of metabolomics, genomics and immune phenotypes reveals the causal roles of metabolites in disease

  Study EGAS00001005348

• Targeted analysis of cell-free circulating tumor DNA is suitable for early relapse and actionable target detection in patients with neuroblastoma

  Study EGAS00001006027

• Analysis of circulating miRNAs for the identification of new prognostic and predictive markers in gastro-entero-pancreatic neuroendocrine tumour (GEP-NET)

  Study EGAS00001007227

• Multi-omics integration reveals only minor long-term molecular and functional sequelae in immune cells of individuals recovered from COVID-19

  Dac EGAC00001002267

• H3K27ac ChIP-seq of lung neuroendocrine tumors

  H3K27ac ChIP-seq of lung neuroendocrine tumors

  Study EGAS50000000057

• MiRNA_Validation

  Rounded Log2 CPM well-expressed miRNA levels in plasma; determined using the HTG EdgeSeq miRNA Whole Transcriptome Assay

  Dataset EGAD00010002752

• MiRNA_TrainTest

  Rounded Log2 CPM well-expressed miRNA levels in plasma; determined using the HTG EdgeSeq miRNA Whole Transcriptome Assay

  Dataset EGAD00010002754

• NGS WGS Data - Unic TDP

  WGS data from the Unicorn-PASS cohort for the Tandem Duplicator Phenotype paper

  Dataset EGAD50000001567

• UMCG Immunogenetics DAC

  DAC for the data generated in the Immunogenetics group in the genetics department of the University Medical Center Groningen

  Dac EGAC50000000785

• DAC for hepatoblastoma sequencing data

  Data Access Committee for sequencing data of hepatoblastoma PDX cell models sequenced under University of Helsinki.

  Dac EGAC50000000548

• Study of PD-1 negative CD8 effector T-cells in advanced HCC with single-cell sequencing

  Study EGAS00001007547

• Soegaard Laboratory Data Access Committee

  Data Access Committee for data generated by the laboratory of Prof. O.S. Soegaard at Aarhus University Hospital.

  Dac EGAC50000000888

• Liquid biopsy-based minimal residual disease monitoring for early risk stratification and decision-making in advanced non-small cell lung cancer

  Dac EGAC50000000832

• A single cell view on host immune transcriptional response to in vivo BCG-induced trained immunity

  Study EGAS00001006990

• Exome sequencing of Resistant BCC samples.

  Exome sequencing of Resistant BCC samples.

  Dataset EGAD00001000887

• Whole_Genome_Sequencing_of_INTERVAL

  Whole genome sequencing of participants from the INTERVAL study.

  Study EGAS00001001355

• ZhongShan Hospital liver tumor single cell sequencing.

  ZhongShan Hospital liver tumor single cell sequencing.

  Study EGAS00001001791

• Exome_sequencing_of_EBV_driven_lymphoma

  Exome sequencing of a case of lethal EBV-driven LPD

  Study EGAS00001001021

• TTN gene targeted sequencing for AMC cohort

  TTN gene targeted sequencing for AMC cohort (n=24)

  Dataset EGAD00001005497

• DNA FASTQ

  TST170 DNA FASTQ files

  Dataset EGAD00001005502

• TST170 Pilot DNA VCF

  TST170 Pilot DNA VCF files

  Dataset EGAD00001006043

• GATCI RNAseq fastqs

  Raw RNA sequence data (fastq) for the GATCI project

  Dataset EGAD00001005810

• Illumina_WXS_BL

  Whole-exome sequencing on Illumina HiSeq2000/2500 of Blood EDTA

  Dataset EGAD00001002093

• SF10320

  SF10320 Unknown.

  Dataset EGAD00001006314

• Exome sequencing of Untreated BCC samples.

  Exome sequencing of Untreated BCC samples.

  Dataset EGAD00001001125

• Sharc-prostate

  Low coverage nanopore sequencing of prostate cancer tumors

  Dataset EGAD00001005473

• AngioPredict CNV and Exome data

  AngioPredict CNV and Exome data

  Dataset EGAD00001004031

• NSCLC targeted

  NSCLC targeted.

  Dataset EGAD00001000889

• WGBS

  Whole Genome Bisulfite Sequencing

  Dataset EGAD00001001119

• TEST3 Dataset

  TEST3 dataset containing 1 FASTQ file with mRNA reads.

  Dataset EGAD00001001920

• CD4 T-Cell ChIP-Seq

  CD4 T-Cell ChIP-Seq

  Dataset EGAD00001002686

• McGill EMC Release 6 data

  McGill EMC Release 6 data

  Dataset EGAD00001002705

• Transcriptome analysis of anaplastic meningiomas

  Transcriptome of anaplastic meingiomas

  Dataset EGAD00001003255

• Whole Genome Sequencing of Normal Singaporean Volunteers

  Whole Genome Sequencing of Normal Singaporean Volunteers

  Dataset EGAD00001004886

• 16S sequencing data for Butyricicoccus safety study

  16S rRNA gene sequencing with Illumina MiSeq (V4 hypervariable region)

  Dataset EGAD00001004406

• Progeria Metagenomics Dataset

  Amplicon sequencing from 45 samples - Amplicons of 16s v3-v4

  Dataset EGAD00001005027

• BC WGS Dataset 3

  Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells

  Dataset EGAD00001001351

• BC WGS Dataset 4

  Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells

  Dataset EGAD00001001353

• Illumina PE WGS data of 9 Egyptian individuals

  High-coverage WGS

  Dataset EGAD00001006037

• Human HiC

  Human HiC

  Dataset EGAD00001003106

• DATA FILES FOR GRUBER SJAMLM7 EXOME

  DATA FILES FOR GRUBER SJAMLM7 EXOME

  Dataset EGAD00001003134

• Exome reads

  Exome reads constituting of FASTQ paired end reads from 5 FHD/FHDL patients

  Dataset EGAD00001003789

• Genome-wide association study of esophageal squamous cell cancer identifies shared and distinct risk variants in African and Chinese populations

  Study EGAS00001007477

• Neurodegenerative_TGS

  An investigation of clonal haematopoiesis in patients with neurodegenerative disease.

  Study EGAS00001002431

• genome-wide cfDNA methylation analysis

  To characterise cfDNA methylome in metastatic prostate cancer

  Study EGAS00001003958

• Bulk RNA data from Wilms Tumors

  Bulk RNA-seq data of pediatric Wilms tumors

  Study EGAS00001006531

• RNAseq of Soft Tissue Sarcomas

  Exon capture RNAseq of 25 soft tissue sarcomas.

  Study EGAS00001007221