NEXome Mini Panel v1.0

NEXome Mini Panel v1.0

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NEXome Mini Panel focuses on the exome associated with clinical inherited diseases, with probe coverage spanning a 16.1 Mb genomic region involving 5650 clinically significant genes and encompassing over 4000 genetic disorders. In comparison to the whole exome panel, the NEXome Mini Panel can be used to rapidly and efficiently detect pathogenic genetic variations within target genes in the human genome. This not only reduces sequencing costs but also significantly shortens data analysis time.
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