WebNov 21, 2014 · Fetal genetic findings for fetal growth restriction without structural malformations at a territory referral center: 10-year experience. GSE212870. Array46 750k test is an in-depht analysis to detect chromosomal alterations, CNVs and SNPs. Download family. Format. SOFT formatted family file (s) SOFT. MINiML formatted family file (s) … WebMay 20, 2015 · We present the R package affy2sv to pre-process Affymetrix CytoScan HD/750k array (also for Genome-Wide SNP 5.0/6.0 and Axiom) in structural variant studies. Results We illustrate the capabilities ...
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WebA chromosomal microarray can detect chromosomal variations (gain and loss of genomic material) at higher resolution than a routine karyotype. The CytoScan® HD assay provides a genome-wide approach that enables high-resolution DNA copy number analysis to detect gains, losses, loss of heterozygosity (LOH), regions identical by descent, and ... Webwith CytoScan™ Amplification Kit (Cat. No. 902975) and CytoScan ™ HD Array Kit (Cat. No. 901833) or CytoScan 750K Array Kit (Cat. No. 901858) to run the CytoScan Assay. Instructions for use Please refer to the CytoScan™ Assay User Guide (Pub. No. 703323) or the CytoScan™ Assay Automated Target Preparation on Affymetrix™ evan wadle pics
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WebThe CMA was conducted with CytoScan 750K array (Affymetrix, USA) with an average resolution of 100 kb. Results: Pathogenic copy number variations (CNVs) were detected in 15 patients by CMA and in two patients by MLPA for four known microdeletion syndromes (Prader-Willi/Angelman syndrome, DiGeorge syndrome, Miller-Dieker syndrome and … WebThe Affymetrix® CytoScan™ 750K Array enables the detection high resolution copy number across the genome as well as providing allelic imbalance information from single … WebCytoScan 750K Suite provides high-resolution coverage of cancer and constitutional genes of interest, along with high-density SNP coverage for loss of heterozygosity (LOH) … first class mail small package