14662 results for "PLOS+ONE+Pennsylvania+German+ACS+language+code+pdc+open+access+study"

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• Cancer genomics project, the University of Tokyo Data Access Committee

  Dac EGAC00001000087

• GEH Data Access Committee

  Dac EGAC00001000139

• BGI Data Access Committee

  Dac EGAC00001000177

• Data access committee of the Prostate Cancer Research Center, University of Tampere, Finland.

  Dac EGAC00001000423

• The Chinese University of Hong Kong Hereditary Spastic Paraplegia Data Access Committee

  Dac EGAC00001000493

• Data Access Committee for the Centre National de Recherche en Génomique Humaine (CNRGH)

  Dac EGAC00001000723

• UT MD Anderson Cancer Center Department of Genomic Medicine Lipoasarcoma Data Access Committee

  Dac EGAC00001000821

• Peking University "Gene & Cognition" Research Group - Data Access Committee

  Dac EGAC00001000856

• Using iPSC-derived neurons to explore cellular phenotypes associated with schizophrenia Data Access Committee.

  Dac EGAC00001000870

• Immune and Metabolic Features of Brain Metastases Melanoma (Cancer Discovery) Data Access Committee

  Dac EGAC00001001216

• DKFZ Medulloblastoma data access committee

  Dac EGAC00001001844

• ALI-cultured PCD and non-PCD patient nasal epithelium transcriptome data access committee

  Dac EGAC00001002882

• The Data Access Committee for Human Olfactory Mucosa Cells (DAC HOM) at UEF

  Dac EGAC00001003404

• Division of Brain Tumor Translational Research, National Cancer Center Japan Data Access Committee

  Dac EGAC50000000366

• human HYPOMAP

  Data access for HYPOMAP raw sequence data and result data objects

  Dac EGAC50000000410

• English Longitudinal Study of Ageing Genome-wide genotyping using the Illumina HumanOmni2.5-8

  These data are for a Genome Wide Association Study (GWAS) in the English Longitudinal Study of Ageing (ELSA, www.ifs.org.uk/elsa), building on the existing ELSA DNA Repository (EDNAR). This will establish a valuable resource for UK and international scientists, giving them access to GWAS genotyping data. Phenotype data, available on request, includes measures of personality, attitudes, behaviours as well as detailed social and economic outcomes; high quality biomarkers and other intermediate phenotypes; a range of more distal phenotypes, such as direct assessments of health (for example, hypertension, diabetes, muscle strength and cognitive function), and the opportunity to analyse existing biological samples for additional biomarkers, including metabolomic studies. Importantly, this resource would be matched with a near identical resource established in the United States for the Health and Retirement Study (HRS), giving the potential for high quality replication studies and comparative analyses.

  Study EGAS00001001036

• GeneScreen, a Population Based, Targeted Genomic Screening Study

  The GeneScreen research study was based at the University of North Carolina (UNC) at Chapel Hill. It brought together researchers from different disciplines, including genetics, clinical medicine, bioethics, sociology, anthropology, psychology, and public health, to study the best ways to offer targeted genetic screening to the general adult population. DNA samples were collected from people who joined GeneScreen to look at a targeted panel of 17 genes. It tested for genetic differences (called mutations) that can cause one of 11 rare, but preventable or treatable conditions, including certain types of cancer and heart disease. Each condition has specific medical advice people can follow with their doctors to prevent or treat a serious health problem. The GeneScreen study was approved by the UNC Institutional Review Board and by the Kaiser Permanente Center for Health Research Institutional Review Board. GeneScreen is funded by the National Human Genome Research Institute of the National Institutes of Health.

  Study phs001817

• Sequence data for study: Mobilization of tissue-resident memory CD4+ T lymphocytes from bone marrow and their contribution to a systemic secondary immune reaction

  Short Description: This study contains 7 RRBS samples, including 3 ex vivo CD4+ Trm (2 x spleen and 1 x bone marrow) and 4 blood tetanus (TT) and measles (Me) antigen-reactive memory CD4+ cells before and one day post DTaP (diphtheria-tetanus-pertussis) and MMR (measles-mumps-rubella) vaccination, respectively (1 x tetanus D0, 1 x tetanus D1, 1 x measles D0, 1 x measles D1). Technology: Illumina HiSeq 2500 Filetype: fastq format

  Dataset EGAD00001007886

• High-grade serous ovarian carcinoma organoids as models of chromosomal instability Data Access Committee

  Dac EGAC00001003204

• Barts Cancer Institute - Follicular Lymphoma Whole Genome Sequencing Project Data Access Committee

  Dac EGAC00001000086

• Data Access Committee: Whole Genome Sequencing of 18 sequential samples from 3 CLL patients

  Dac EGAC00001000221

• Department of Pathology and Tumor Biology, Kyoto University Data Access Committee

  Dac EGAC00001000273

• Oxford Human Islet Data Access Committee

  Dac EGAC00001000335

• Division of Cancer Genomics, National Cancer Center Research Institute Data Access Committee

  Dac EGAC00001000957

• Expanding the neurodevelopmental phenotypes of individuals with de novo KMT2A variants Data Access Committee

  Dac EGAC00001001147