(2012) zCall: a rare variant caller for array-based genotyping . Bioinformatics 28 : 2543–2545 [ PMC free article ] [ PubMed ]Goldstein JI, Crenshaw A, Carey J, Grant GB, Maguire J, Fromer M, et al. zCall: a rare variant caller for array-based genotyping. Bioinformatics. 2012; ...
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 ...
4. Syvanen AC (2005) Toward genome-wide SNP genotyping. Nat Genet 37 Suppl:S5–S10 Article PubMed Google Scholar 5. Oliphant A, Barker DL, Stuelpnagel JR, Chee MS (2002) BeadArray technology: Enabling an accurate, cost-effective approach to high-throughput genotyping. Biotechniques Suppl:...
Comparative genomics and DNA array-based genotyping of pandemic Staph- ylococcus aureus strains encoding Panton-Valentine leukocidin. Clin Microbiol Infect 2007;13:236-49.Monecke, S., B. Berger-Ba篓chi, G. Coombs, A. Holmes, I. Kay, A. Kearns, H.-J. Linde, F. O'Brien, P. ...
Array-based genotyping in S.cerevisiae using semi-supervised clustering. Bourgon R,Mancera E,Brozzi A, et al. Bioinformatics . 2009... R Bourgon,E Mancera,A Brozzi,... 被引量: 0发表: 0年 Array-based genotyping in (2009) Array- based genotyping in S. cerevisiae using semi- supervised ...
but this approach is limited by the need for a large overlap in variants across genotyping arrays and the scarcity of non-European controls. We developed and validated a protocol, Genotyping Array-WGS Merge (GAWMerge), for combining genotypes from arrays and whole-genome sequencing, ensuring compl...
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...
SNP genotyping, based on analysis of informative SNP loci with opposing homozygous parental genotypes, confirmed partial monosomies associated with inheritance of unbalanced translocation in surplus embryos. We have developed a universal MDA-SNP array technique for chromosome CN analysis in single ...
Amplicon resequencing is robust, reliable, and unbiased and has the potential for scalable sample preparation for small and large research or clinical studies, increasing accurate genotyping for improved outcomes. We have developed a cost-efficient FLG genotyping method (∼10 times cheaper than exome...
their termini, shown in the figure as increasing length of the open square. This enables genotyping of 6 sequential bases in the hybridized tag205or206, using either single-base extension of 3′-up probes or base-specific ligation to 5′-PO4probes. Each of the probes in the probe set ...