zCall: a rare variant caller for array-based genotyping. Bioinformatics 2012; 28: 2543-2545.Goldstein et al. zCall: A Rare Variant Caller for Array-based Genotyping. Bioinformatics. 2012 Oct 1;28(19):2543-5Goldstein JI, Crenshaw A, Carey J, et al. zCall: a rare variant caller for ...
There is a demand for technologies that allow the interrogation of large numbers of SNP polymorphisms, both in whole-genome panels and in smaller custom designed sets, to attempt to elucidate the nature of complex disease through linkage and association
Innovating Molecular Breeding with Streamlined High Throughput Genotyping and Lightning Quick DNA extraction View webinar Feature article: April 28, 2025 The path to precision medicine in Indonesia Read article Research publication: March 03, 2025 ...
Array-based genotyping in S.cerevisiae using semi-supervised clustering. Bourgon R,Mancera E,Brozzi A, et al. Bioinformatics . 2009... Richard,Bourgon,Eugenio,... - 《Bioinformatics》 被引量: 15发表: 2009年 Array-based genotyping in using semi-supervised clustering Array-based genotyping in S...
is not fully utilized. Therefore, those rare variants and large insertions/deletions only detected in WGS data were lost during the extraction and merging processes (Supplementary Table3). However, coming from a case-only dataset with array-based genotyping, the dominant scenario for use of GAWMer...
Chambert K, Stevens C; Swedish Schizophrenia Consortium; ARRA Autism Sequencing Consortium, Sklar P, Hultman CM, Purcell S, McCarroll SA, Sullivan PF, Daly MJ, Neale BM. zCall: a rare variant caller for array-based genotyping: Genetics and population analysis. Bioinformatics. 2012 Oct 1;28...
Find ready-to-use microarray kits for a wide variety of genotyping and epigenetics studies, or use custom kits for genotyping of any species.
GenomeStudio software provides an integrated platform for data analysis of microarray-based genotyping assays, with a user-friendly graphical interface.
(1)WGA:根据检测方法和突变类型的不同,分别采用多次退火环状循环扩增(multiple annealing and looping-based amplification cycles, MALBAC, 苏州亿康)或多重置换扩增(multiple displacement amplification, MDA, 德国Qiagen)两种方法进行WGA,...
Array based comparative genomic hybridization (array CGH) has emerged as a powerful tool for detecting gene copy number variants implicated in many disease states. Simple, robust genomic DNA labeling reagents and removal of free dye and nucleotides are two of the most critical components dete...