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MGICare Single Gene Genomic Disease Phasing and Chromosome Copy Number Variation Sequencing Library Prep Set
MGICare Single Gene Genomic Disease Phasing and Chromosome Copy Number Variation Sequencing Library Prep Set is specifically designed for the MGI High-throughput series sequencing platforms. This library prep kit is optimized to prepare a whole genome-wide and Thalassemia genes region enriched library from human genomic DNA and single-cell(or multiple cells)multiple displacement amplification (MDA) products. Only one library preparation is needed to detect both chromosome copy number variations and Thalassemia gene mutation.
The kit uses multiplex PCR amplification technology combined with NGS sequencing technology and PGS/PGD integration software to accurately identify chromosomal copy number variant and thalassemia in embryos.

Characteristics

PGS and PGD detection can be completed at one library preparation:The whole genome and target capture are performed in one tube
Easy to Use:Simple protocol and short operation time, suitable for automated library preparation instrument
Applicable for detection of chromosomal copy number variations larger than 16Mb and the situation of thalassaemia
HLA matching helps probands regain health

Specification

Product Name MGICare Single Gene Genomic Disease Phasing and Chromosome Copy Number Variation Sequencing Library Prep Set
PN. 1000013705
Specification

48 rxn

Assay Time ~5 h
Hands-On Time ~2 h
Sample types 300ng Human genome DNA、single cell or multiple cells MDA products
Applications Chromosomal copy number variation detection and the detection of thalassemia and HLA matching
Platform Compatibility MGISEQ-200、MGISEQ-2000 and so on
Recommended Read Length SE50+10
Recommended software PGS/PGD Integration software
Recommended sequencing data

10 million raw reads

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