Title |
Pedigree and genotyping quality analyses of over 10,000 DNA samples from the Generation Scotland: Scottish Family Health Study
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Published in |
BMC Medical Genomics, March 2013
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DOI | 10.1186/1471-2350-14-38 |
Pubmed ID | |
Authors |
Shona M Kerr, Archie Campbell, Lee Murphy, Caroline Hayward, Cathy Jackson, Louise V Wain, Martin D Tobin, Anna Dominiczak, Andrew Morris, Blair H Smith, David J Porteous |
Abstract |
Generation Scotland: Scottish Family Health Study (GS:SFHS) is a family-based biobank of 24,000 participants with rich phenotype and DNA available for genetic research. This paper describes the laboratory results from genotyping 32 single nucleotide polymorphisms (SNPs) on DNA from over 10,000 participants who attended GS:SFHS research clinics. The analysis described here was undertaken to test the quality of genetic information available to researchers. The success rate of each marker genotyped (call rate), minor allele frequency and adherence to Mendelian inheritance are presented. The few deviations in marker transmission in the 925 parent-child trios analysed were assessed as to whether they were likely to be miscalled genotypes, data or sample handling errors, or pedigree inaccuracies including non-paternity. |
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Geographical breakdown
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Germany | 1 | 20% |
Unknown | 1 | 20% |
Demographic breakdown
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Members of the public | 2 | 40% |
Practitioners (doctors, other healthcare professionals) | 1 | 20% |
Mendeley readers
Geographical breakdown
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Demographic breakdown
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Student > Ph. D. Student | 11 | 17% |
Professor | 7 | 11% |
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Professor > Associate Professor | 4 | 6% |
Other | 10 | 15% |
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Social Sciences | 3 | 5% |
Other | 8 | 12% |
Unknown | 14 | 22% |