VISTA™

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VISTA™ CARRIER SCREENING MAX
Screening for more than 80,000 mutations associated with 800 recessive genetic conditions
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VISTA™ CARRIER SCREENING MINI PANEL
Screening for more than 5,400 mutations associated with 11 recessive genetic conditions
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VISTA™ CARRIER SCREENING TARGETED PANEL 2.0
Screening for more than 11,000 mutations associated with 172 recessive genetic conditions
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VISTA™ CHROMOSOME SEQEUNCING – 100K
Chromosome sequencing of aneuploidy of all chromosomes, >100 Kb of deletions or duplications to investigate the causes of infertility or miscarriage.
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VISTA™ CHROMOSOME SEQUENCING – 1M
Chromosome sequencing of aneuploidy of all chromosomes, >100 Mb of deletions or duplications to investigate the causes of infertility or miscarriage.
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VISTA™ THALASSEMIASEQ
Detect HBA1, HBA2, HBB genes at one time and detect more than 508 thalassemia mutations & more than 1000 Hb mutations.
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