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Twist Alliance VCGS Exome-40.1 MB (2, 12, or 96 reactions)

Streamline the identification of heritable disease-linked alleles, be it through carrier screening or pre- and post-natal testing.

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Drawing on decades of experience in clinical genomics, Victorian Clinical Genetics Services (VCGS) has partnered with Twist to design a diagnostic panel—Twist Alliance VCGS Exome - 40.1 MB—that covers the whole exome, with dedicated coverage boosting over clinically relevant genes (Mendeliome). In designing this panel, special care was given to ensuring additional coverage of clinically relevant loci that fall outside the gene coding regions traditionally targeted by exomes (i.e. known pathogenic loci in non-coding regions).

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