Genotype call for chromosomal deletions using read-depth from whole genome sequence variants in cattle

Publikation: KonferencebidragPosterForskning

  • Md Mesbah-Uddin, Animal Genetics and Integrative Biology, UMR 1313 GABI, INRA, AgroParisTech, Université Paris-Saclay, 78350 Jouy-en-Josas, France.
  • ,
  • Bernt Guldbrandtsen
  • ,
  • Mogens Sandø Lund
  • Goutam Sahana
We presented a deletion genotyping (copy-number estimation) method that leverages population-scale whole genome sequence variants data from 1K bull genomes project (1KBGP) to build reference panel for imputation. To estimate deletion-genotype likelihood, we extracted read-depth (RD) data of all the bi-allelic variants within a given deletion locus, and fitted a Gaussian mixture model to the observed RD. We validated our method on brachyspina associated deletion of chromosome 21 (Chr21:21,184,869-21,188,202), which was segregating in our deletion-discovery population of Holstein cattle. We analysed the RD data of 55 progeny tested Holstein bulls with published recessive code for brachyspina (8 carriers and 47 non-carriers) along with 5 carriers from the discovery population (confirmed by assembling the breakpoint sequences). Using our approach we were able to genotype the carriers and non-carriers with 95% accuracy, and a false discovery rate of 18.8%.
Udgivelsesårfeb. 2018
StatusUdgivet - feb. 2018
BegivenhedThe 11th World Congress on Genetics Applied to Livestock Production - Aotea Centre, Auckland 1010, Auckland, New Zealand
Varighed: 11 feb. 201816 feb. 2018
Konferencens nummer: 11


KonferenceThe 11th World Congress on Genetics Applied to Livestock Production
LokationAotea Centre, Auckland 1010
LandNew Zealand

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