22938 results for "ega"

in 110.78 milliseconds.

• 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

• Biomarker data

  Biomarker data including the time point of sample collection, tumor content and ERBB2 gene expression.

  Dataset EGAD00001009415

• Chip-Seq

  27 Chip-Seq samples from Human CD4+ T cells

  Dataset EGAD00001010181

• Cancers of Unknow Primary

  genetic data of 14 rigorously selected CUP samples

  Dataset EGAD00001009426

• WGS Huh7 cell lines

  Whole Genome Sequencing of Huh7 cell lines

  Dataset EGAD00001001386

• RNA-seq data for NRF2 study

  RNA-seq data for clinical samples

  Dataset EGAD00001002243

• BotSeq sequences1

  This is the first dataset for the Botseq sequencing project

  Dataset EGAD00001002263

• Melanoma multi site metastases

  These are caveman, pindel and sequenza calls for the metastatic melanoma exomes within this study.

  Dataset EGAD00001005487

• Nevi exome sequencing

  8 matched pair melanocytic nevi Agilent SureSelect Human All Exon V5 plus UTR

  Dataset EGAD00001006011

• Plasma DNA profile in DNASE1L3 deficiency

  Plasma DNA profile in DNASE1L3 deficiency

  Dataset EGAD00001006216

• Expression profiles and genetic makeup of agnospheres.

  WES performed on 15 CUP-derived samples

  Dataset EGAD00001006668

• H3K4me3, IgG, and Input ChIP-seq in overexpression of pLV Control, CS-FL and CS-ΔEx4 in SW1116 cells.

  none

  Study EGAS00001008121

• Gene signature for predicting homologous recombination deficiency in triple-negative breast cancer

  We developed a gene expression-based classifier for homologous recombination deficiency (HRD) in breast cancer patients using WES and RNA-seq data obtained from 94 TNBC samples from a Malaysian hospital-based cohort (MyBrCa). This classifier was able to predict for high levels of a mutational signature associated with HRD in an additional MyBrCa TNBC validation cohort (this EGA study) as well as in TNBCs from TCGA. We also validated the classifier on a NanoString platform with both fresh frozen and FFPE tissue.

  Study EGAS00001006518

• BRERUNO

  Dac EGAC00001003277

• Human transcriptomic (RNA-Seq) and epigenomic (ATAC-Seq) data of early B-cell lineage (bulk and single-cell) DAC

  Dac EGAC00001003265

• METABRIC data access committee

  Dac EGAC00001000484

• Data Access Committee of divisions B060 and B062, German Cancer Research Center (DKFZ)

  Dac EGAC00001001626

• EGAD00010000280

  CLL Expression array

  Dataset EGAD00010000280

• EGAD00010000516

  Samples from the Pomak Villages in Greece, Pomak isolate

  Dataset EGAD00010000516

• EGAD00010000538

  28 unlinked autosomal microsatellite loci for 20 African and 4 philippine populations

  Dataset EGAD00010000538

• EGAD00010000564

  HipSci - Healthy Normals - Expression Array - May 2014

  Dataset EGAD00010000564

• EGAD00010000568

  HipSci - Healthy Normals - Methylation Array - May 2014

  Dataset EGAD00010000568

• Breast Cancer Follow Up Series

  Breast Cancer Follow Up Series

  Dataset EGAD00001000066

• Cancer Single Cell Sequencing

  Cancer Single Cell Sequencing

  Dataset EGAD00001000067

• Acute Lymphoblastic Leukemia Exome sequencing

  Acute Lymphoblastic Leukemia Exome sequencing

  Dataset EGAD00001000089

• Glioma cell lines rearrangement screen

  Glioma cell lines rearrangement screen

  Dataset EGAD00001000090

• Pancreatic adenocarcinoma QCMG 20120201

  Pancreatic adenocarcinoma QCMG 20120201

  Dataset EGAD00001000096

• Burden of Disease in Sarcoma

  Burden of Disease in Sarcoma

  Dataset EGAD00001000127

• Lung Cancer Whole Genomes

  Lung Cancer Whole Genomes

  Dataset EGAD00001000144

• DATA FILES FOR SJOS

  DATA FILES FOR SJOS

  Dataset EGAD00001000159

• DATA FILES FOR SJLGG

  DATA FILES FOR SJLGG

  Dataset EGAD00001000161

• Whole Genome Methylation in CLL

  Whole Genome Methylation in CLL

  Dataset EGAD00001000177

• Gene Discovery in Age-Related Hearing Loss

  Gene Discovery in Age-Related Hearing Loss

  Dataset EGAD00001000198

• Screening for abnormal CGI methylation in primary colorectal tumours

  Screening for abnormal CGI methylation in primary colorectal tumours

  Dataset EGAD00001000213

• UK10K_NEURO_ASD_BIONED REL-2012-07-05

  EGAD00001000228_UK10K_NEURO_ASD_BIONED_REL_2012_07_05

  Dataset EGAD00001000228

• UK10K_NEURO_ASD_FI REL-2012-07-05

  EGAD00001000229_UK10K_NEURO_ASD_FI_REL_2012_07_05

  Dataset EGAD00001000229

• UK10K_NEURO_ASD_GALLAGHER REL-2012-07-05

  EGAD00001000230_UK10K_NEURO_ASD_GALLAGHER_REL_2012_07_05

  Dataset EGAD00001000230

• UK10K_NEURO_ASD_SKUSE REL-2012-07-05

  EGAD00001000231_UK10K_NEURO_ASD_SKUSE_REL_2012_07_05

  Dataset EGAD00001000231

• UK10K_NEURO_IOP_COLLIER REL-2012-07-05

  EGAD00001000235_UK10K_NEURO_IOP_COLLIER_REL_2012_07_05

  Dataset EGAD00001000235

• UK10K_NEURO_IMGSAC REL-2012-07-05

  EGAD00001000239_UK10K_NEURO_IMGSAC_REL_2012_07_05

  Dataset EGAD00001000239

• UK10K_NEURO_ASD_MGAS REL-2012-07-05

  EGAD00001000242_UK10K_NEURO_ASD_MGAS_REL_2012_07_05

  Dataset EGAD00001000242