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Towards the detection of copy number variation from single sperm sequencing in cattle.
Yang L, Gao Y, Oswalt A, Fang L, Boschiero C, Neupane M, Sattler CG, Li CJ, Seroussi E, Xu L, Yang L, Li L, Zhang H, Rosen BD, Van Tassell CP, Zhou Y, Ma L, Liu GE. Yang L, et al. Among authors: xu l. BMC Genomics. 2022 Mar 17;23(1):215. doi: 10.1186/s12864-022-08441-8. BMC Genomics. 2022. PMID: 35300589 Free PMC article.
Bovine exome sequence analysis and targeted SNP genotyping of recessive fertility defects BH1, HH2, and HH3 reveal a putative causative mutation in SMC2 for HH3.
McClure MC, Bickhart D, Null D, Vanraden P, Xu L, Wiggans G, Liu G, Schroeder S, Glasscock J, Armstrong J, Cole JB, Van Tassell CP, Sonstegard TS. McClure MC, et al. Among authors: xu l. PLoS One. 2014 Mar 25;9(3):e92769. doi: 10.1371/journal.pone.0092769. eCollection 2014. PLoS One. 2014. PMID: 24667746 Free PMC article.
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