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Showing 17–32 of 42 results

Sentis™ HEREDITARY PANCREATIC CANCER
Screening 12 inherited genes associated with pancreas cancer
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Sentis™ HEREDITARY PROSTATE CANCER
Screening 23 inherited genes associated with prostate cancers
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Sentis™ HEREDITARY RETINOBLASTOMA
Screening RB1 inherited genes associated with eye cancer
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Sentis™ HRD SCORE
Genetic testing to access genomics instability indicators in cancer cells to seek for possibility of using PARPi treatment
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SEQHPV™ HPV TEST
HPV screening that by detecting 14 types of HPV genotypes, including HPV 16 & 18 and 2 low-risk HPV genotypes
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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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WEGENE STANDARD
DNA testing that is personalised to enhance your lifestyle, covering 750+ reports across 11+ categories.
RM2,499.00 Add to cart
WEGENE WGS
Whole Genome Sequencing of human genome for personalised guidance for healthy lifestyle, covering 900+ reports across 12+ categories.
RM6,999.00 Add to cart
XOME EXPRESS
Genetic exome sequencing for fast identification of top 20 variants reports based on BGI’s automated variant analysis pipeline
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XOME EXPRESS (TRIO)
Screens up to 3 related individual on top of regular XOME Express
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XOME GENETIC TESTING FOR 21-OHD CONGENITAL ADRENAL HYPERPLASIA
Sanger sequencing testing for 21-Hydroxylase Deficient Congenital Adrenal Hyperplasia with CYP21A2 gene
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