Results 131 to 140 of about 10,451,845 (193)

Copy Number Variation in Common Disease

Thyroid®, 2011
Brand, O, Gough, S
openaire   +2 more sources

<i>RNU2-1</i> gene copy number variations do not affect serum levels of miR-1246 as a biomarker for lung adenocarcinoma. [PDF]

Exp Ther Med
Ueda M, Sato S, Miyagi Y, Aiso T.
europepmc   +1 more source

Decoding clone evolution in HER2 amplified breast cancer through single-cell and spatial transcriptomics analysis of copy number variations. [PDF]

Sci Rep
Yang J, Li Y, Luo S, Wang J, Duan Y.
europepmc   +1 more source

Clinical Implications and Limitations of Noninvasive Prenatal Testing for Detecting Fetal Copy Number Variations: A Multicenter Study in Shaanxi Province, China. [PDF]

Med Sci Monit
Wang H, Zhang L, Yang T, Jia Y, Liu R, Jia Z, Liu Y, Bai G.   +7 more
europepmc   +1 more source

Correction to: Enhancing interpretation of clinical disease-associated copy number variations from multiple sequencing strategies with CNVSeeker. [PDF]

Bioinformatics
europepmc   +1 more source

Tool Comparison for Detecting Tumour Cells in Endometrial Cancer via Single-Cell Copy Number Variations Analysis. [PDF]

J Cell Mol Med
Dugo E, Piva F, Giulietti M, Giannella L, Ciavattini A.   +4 more
europepmc   +1 more source

ZIPcnv: accurate and efficient inference of copy number variations from shallow whole-genome sequencing. [PDF]

Bioinformatics
Xue Z, Zeng J, Wang X, Yuan J, Wang T, Lai X, Wang L, Wang Y, Zhu H, Jin X, Wang J.   +10 more
europepmc   +1 more source

Identification of copy number variations through whole genome resequencing between Jiuyishan and Hyplus rabbits. [PDF]

Front Vet Sci
Wang Y, Wang J, Ding H, Yang L, Zhao H, Huang D.   +5 more
europepmc   +1 more source

Combining pangenomics and population genetics finds chromosomal re-arrangements, diversified chromosome segments, copy number variations and transposon polymorphisms in wheat and rye powdery mildew. [PDF]

PLoS Pathog
Sotiropoulos AG, Müller MC, Kunz L, Graf JP, Kiss L, Hückelhoven R, Schlagenhauf E, Keller B, Wicker T.   +8 more
europepmc   +1 more source

Residual risk of clinically significant copy number variations in fetuses with ultrasonographic soft markers following exclusion of non-invasive prenatal screening-detectable findings. [PDF]

Arch Gynecol Obstet
Liang Y, Zhou R, Liu T, Gao J, Xu Y, Huang M, Meng L, Huo H, Zhang Q, Wu Y, Xu Z, Wang Y.   +11 more
europepmc   +1 more source