Genomics Service—Illumina Iscan

Rely on CD BioSciences' experienced genomics services to deliver high-quality, interpretable results using highly sensitive PCR, real-time PCR, NGS technologies, and advanced data analysis. All of your genomics research needs can be met with our highly flexible and customizable platform and our long experience in analyzing preclinical research samples.

Name of the Instrument/Platform

Illumina Iscan

MANUFACTURER:

Illumina

Introduction

• Humancyto SNP-12V2.1
The 12-sample HumanCytoSNP-12 BeadChip is a powerful, whole-genome scanning panel designed for efficient, high-throughput analysis of genetic and structural variations that are most relevant to human disease.
Complete panel of genome-wide tag single nucleotide polymorphisms (SNPs) and markers targeting all regions of known cytogenetic importance, incorporating ~300,000 "best of the best" SNPs with the highest tagging power
1. Average SNP call rates and reproducibility of > 99.9%, and low noise for copy number measurements
2. Detect many types and sizes of structural variation in the human genome that affect phenotypes, including duplications, deletions, amplifications, copy-neutral loss of heterozygosity (LOH), and mosaicism
3. Process up to 12 samples in parallel, increasing sample throughput and decreasing experimental variability
4. Process samples using the single-tube, PCR-free Infinium HD Assay that requires only 200ng DNA per sample
The HumanCytoSNP-12 Be

Summary

The iScan System can scan thousands of array samples per day, without sacrificing data quality or reproducibility. It supports our expansive portfolio of genetic analysis assays, from high-throughput genotyping to DNA methylation analysis.

CD BioSciences offers you Illumina Iscan-based genomic services. If you are interested, please feel free to contact us for more information.

For research use only, not intended for any clinical use.

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