CentoScreen™

 | Post date: 2017/12/23 | 
CentoScreen™

NGS Analysis of 331 genes for carrier screening
 
1. Sequence variants including
- known deep intronic pathogenic variants
- splicing
- regulatory
- any known mutation in CentoMD® 4.0 or HGMD® Professional 2017.3.


Covers >99% of  regions in CCDS 

>99% coverage at 20x of targeted bases

2. Structural variants

3. Repeat expansion


Tel/Fax:+98-21 86035745- 88926847- 86034940
Email: info@gsdseq.ir
https://t.me/genoscop

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