Results 131 to 140 of about 253,893 (144)

The role of AMY1 gene copy number variation in dental caries susceptibility: insights from a Turkish population. [PDF]

BMC Oral Health
Hatipoğlu Ö, Saydam F.
europepmc   +1 more source

A benchmarking study of copy number variation inference methods using single-cell RNA-sequencing data. [PDF]

Precis Clin Med
Chen X, Fang LT, Chen Z, Chen W, Wu H, Zhu B, Moos M, Farmer A, Zhang X, Xiong W, Gong S, Jones W, Mason CE, Wu S, Xiao C, Wang C.   +15 more
europepmc   +1 more source

Detection of <i>Ureaplasma parvum</i> in amniotic fluids via reanalysis of prenatal copy number variation sequencing data: an exploratory study. [PDF]

Front Cell Infect Microbiol
Wang G, Chen W, Chen X, Hou H, Zhang J, Han Z.   +5 more
europepmc   +1 more source

The role of gene copy number variation in antimicrobial resistance in human fungal pathogens. [PDF]

NPJ Antimicrob Resist
Jay A, Jordan DF, Gerstein A, Landry CR.
europepmc   +1 more source

Evaluation of the relationship between cytochrome P450 (CYP) 1A2 gene copy number variation and CYP1A2 protein content and enzyme activity in canine liver. [PDF]

Front Vet Sci
Zamora FG, Bigelow H, Yang H, Jimenez TP.   +3 more
europepmc   +1 more source

A copy number variation detection method based on OCSVM algorithm using multi strategies integration. [PDF]

Sci Rep
Zhou M, Dong J, Jiang H, Zhao Z, Yuan T.
europepmc   +1 more source

Genome-wide copy number variation association study in anorexia nervosa. [PDF]

Mol Psychiatry
Walker A, Karlsson R, Szatkiewicz JP, Thornton LM, Yilmaz Z, Leppä VM, Savva A, Lin T, Sidorenko J, McRae A, Kirov G, Davies HL, Fundín BT, Chawner SJRA, Song J, Borg S, Wen J, Watson HJ, Munn-Chernoff MA, Baker JH, Gordon S, Berrettini WH, Brandt H, Crawford S, Halmi KA, Kaplan AS, Kaye WH, Mitchell J, Strober M, Woodside DB, Pedersen NL, Parker R, Jordan J, Kennedy MA, Birgegård A, Landén M, Martin NG, Sullivan PF, Bulik CM, Wray NR.   +39 more
europepmc   +1 more source

Genetic etiology of 283 Chinese individuals with epilepsy using copy number variation sequencing and whole exome sequencing: a single-center cohort study. [PDF]

BMC Med Genomics
Hu J, Xin M, Liu J, Li H, Li X, Chen L, Yang P, Zhao H, Sun P, Gao G, Feng H, Li Z, Xiao G, Li Y, Li K, Xu X.   +15 more
europepmc   +1 more source

Application of copy number variation sequencing combined with whole exome sequencing in prenatal left-right asymmetry disorders. [PDF]

BMC Genomics
Qin Y, Senglong M, Touch K, Xiao J, Fang R, Kang Q, Fan L, Li S, Liu J, Wu J, Wu Y, Shi X, Liu H, Gong X, Lin X, Feng L, Chen S, Li W.   +17 more
europepmc   +1 more source