14308 results for ""Pennsylvania+German"+ACS+study+'Socius'+open+access"

in 11.64 milliseconds.

• MD Anderson GU Data Access Committee

  Dac EGAC00001002356

• Data Access Committee for data from EGAS00001002864

  Dac EGAC00001003487

• Data Access Committee for data from EGAS00001007832

  Dac EGAC00001003500

• Data Access Committee for data from EGAS00001007819

  Dac EGAC00001003501

• UTHSCSA HCC Team Data Access Commitee

  Dac EGAC00001003351

• Dusseldorf/Lisbon Data Access Commitee

  Dac EGAC00001002758

• CCRI NFAT project data access committee

  Dac EGAC00001003280

• General DAC

  General Data Access Committee.

  Dac EGAC50000000184

• UVM Data Access Commitee

  Dac EGAC00001002078

• Francis Crick Institute Data Access Committee

  Dac EGAC50000000111

• Data Access Committee for data from EGAS00001007904

  Dac EGAC00001003512

• Data Access Committee for data from EGAS00001008107

  Dac EGAC00001003568

• EXPIRED - Data Access Committee Princess Maxima Center

  Dac EGAC00001003259

• EXPIRED - Data Access Committee Princess Maxima Center

  Dac EGAC00001003355

• Auristone Data Access Committee

  Auristone DAC

  Dac EGAC50000000875

• Whole genome sequencing of six ethnic groups from Burkina Faso, Cameroon, and Tanzania

  We conducted low-coverage (~10x) sequencing of six ethnic groups from three malaria-endemic countries in sub-Saharan Africa, with the aim of characterising genetic diversity and improving imputation performance for genotyped samples in these populations. This data is part of a pre-publication release and is available under managed access. Please see https://www.malariagen.net/data/terms-use/human-gwas-data for more information on MalariaGEN data access policies. The purpose of the project was to support the discovery and understanding of genetic variants that influence human disease. Specifically defined goals were: a. the discovery of single nucleotide variants at frequencies of 1% or higher in diverse populations, b. even more comprehensive discovery (variants down to frequencies of 0.1 - 0.5%) in functional gene regions, and c. discovery of structural variants, such as copy number variants, other insertions and deletions, and inversions, including sequence-level understanding of breakpoints.

  Study EGAS00001003648

• Melanoma Institute Australia Data Access Committee

  Dac EGAC00001003075

• Japanese genotype Data Access Commeitee

  Dac EGAC00001003107

• Small intestinal plasma cells data access committee

  Dac EGAC00001001079

• MS Risk Gene RNAseq Data Access Committee

  Dac EGAC00001003249

• Berlin Neuroblastoma Liquid Biopsy Data Access Committee

  Dac EGAC00001003314

• Data Access Commitee of mantle cell lymphoma

  Dac EGAC00001001119

• Lung cancer RNA Seq Data Access Committee

  Dac EGAC00001003317

• Human Subsistence - chemosensation genomics - Data access Committee

  Dac EGAC00001003272

• DKFZ OE0214 Data Access Committee

  Dac EGAC00001002156