Labs brochures - for Providers

This collection includes all of our SEQUENOM LABORATORIES provider-oriented brochures for MaterniT21 PLUS, VisibiliT, HerediT, SensiGene RHD, RetnaGene and NextView lines of laboratory-developed tests.

  • Spanish MaterniT 21 PLUS core patient brochure_Rep-1053-v1-0217

    Spanish MaterniT 21 PLUS core patient brochure_Rep-1053-v1-0217

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  • Interested in learning how we can support your prenatal NIPT needs?

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  • Spanish MaterniT 21 PLUS ESS patient brochure_Rep-1054-v1-0217

    Spanish MaterniT 21 PLUS ESS patient brochure_Rep-1054-v1-0217

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  • Expanding Noninvasive Prenatal Testing (NIPT) to Average Risk: MaterniT® 21 PLUS Performance in the Average Risk vs. High Risk Population

    Expanding Noninvasive Prenatal Testing (NIPT) to Average Risk: MaterniT® 21 PLUS Performance in the Average Risk vs. High Risk Population

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  • Optimized Detection of 22q11.2 Deletions Using Whole Genome Sequencing

    Optimized Detection of 22q11.2 Deletions Using Whole Genome Sequencing

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  • Five years of precision – cfDNA as a case example

    Five years of precision – cfDNA as a case example

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  • Success of NIPT based on Maternal Weight and Gestational Age

    Success of NIPT based on Maternal Weight and Gestational Age

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  • MaterniT 21® PLUS provider brochure

    MaterniT 21® PLUS provider brochure

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  • Abnormal ultrasound and increased yield of abnormal results with genome-wide cfDNA analysis

    Abnormal ultrasound and increased yield of abnormal results with genome-wide cfDNA analysis

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  • Expanding noninvasive prenatal testing (NIPT) for screening of unbalanced translocations

    Expanding noninvasive prenatal testing (NIPT) for screening of unbalanced translocations

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  • Genome wide detection of chromosomal gains and losses greater than 7Mb by cfDNA analysis

    Genome wide detection of chromosomal gains and losses greater than 7Mb by cfDNA analysis

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  • Clinical experience of trisomy 16 and 22, and microdeletion detection by noninvasive prenatal testing (NIPT)

    Clinical experience of trisomy 16 and 22, and microdeletion detection by noninvasive prenatal testing (NIPT)

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  • Automated genomic interpretation of sub-chromosomal fetal copy number variation by sequencing circulating cell-free DNA from maternal plasma

    Automated genomic interpretation of sub-chromosomal fetal copy number variation by sequencing circulating cell-free DNA from maternal plasma

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  • Circulating cell-free DNA screening for fetal aneuploidy- the Newton-Wellesley Hospital Maternal Fetal Medicine experience

    Circulating cell-free DNA screening for fetal aneuploidy- the Newton-Wellesley Hospital Maternal Fetal Medicine experience

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  • Identification of 22q11 microdeletions by noninvasive prenatal testing (NIPT) - the clinical experience

    Identification of 22q11 microdeletions by noninvasive prenatal testing (NIPT) - the clinical experience

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  • Karyotype-level noninvasive prenatal testing by sequencing of circulating cell-free DNA from maternal plasma

    Karyotype-level noninvasive prenatal testing by sequencing of circulating cell-free DNA from maternal plasma

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  • Noninvasive prenatal testing aids in detecting parental balanced translocation and highlights limitations of karyotyping

    Noninvasive prenatal testing aids in detecting parental balanced translocation and highlights limitations of karyotyping

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  • Rings and things- Noninvasive prenatal testing¹s unique view of the biology and embryology behind chromosomal ring formation and segregation

    Rings and things- Noninvasive prenatal testing¹s unique view of the biology and embryology behind chromosomal ring formation and segregation

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  • Two cases of Wolf-Hirshhorn syndrome detected by noninvasive prenatal testing (NIPT)

    Two cases of Wolf-Hirshhorn syndrome detected by noninvasive prenatal testing (NIPT)

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  • HerediT CF provider sheet

    HerediT CF provider sheet

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  • HerediT UNIVERSAL Patient Brochure Mar 2015

    HerediT UNIVERSAL Patient Brochure Mar 2015

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