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Deep genome sequencing and variation analysis of 13 inbred mouse strains defines candidate phenotypic alleles, private variation, and homozygous truncating mutations
Anthony G. Doran, Kim Wong, Jonathan Flint, David J. Adams, Kent W. Hunter, Thomas M. Keane
doi: https://doi.org/10.1101/039131
Anthony G. Doran
1Wellcome Trust Sanger Institute, Hinxton, Cambridge, CB10 1HH, UK
Kim Wong
1Wellcome Trust Sanger Institute, Hinxton, Cambridge, CB10 1HH, UK
Jonathan Flint
2The Wellcome Trust Centre for Human Genetics, Roosevelt Drive, Oxford OX3 7BN, UK
David J. Adams
1Wellcome Trust Sanger Institute, Hinxton, Cambridge, CB10 1HH, UK
Kent W. Hunter
3Laboratory of Cancer Biology and Genetics, NCI, NIH
Thomas M. Keane
1Wellcome Trust Sanger Institute, Hinxton, Cambridge, CB10 1HH, UK
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Posted February 09, 2016.
Deep genome sequencing and variation analysis of 13 inbred mouse strains defines candidate phenotypic alleles, private variation, and homozygous truncating mutations
Anthony G. Doran, Kim Wong, Jonathan Flint, David J. Adams, Kent W. Hunter, Thomas M. Keane
bioRxiv 039131; doi: https://doi.org/10.1101/039131
Deep genome sequencing and variation analysis of 13 inbred mouse strains defines candidate phenotypic alleles, private variation, and homozygous truncating mutations
Anthony G. Doran, Kim Wong, Jonathan Flint, David J. Adams, Kent W. Hunter, Thomas M. Keane
bioRxiv 039131; doi: https://doi.org/10.1101/039131
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