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Poster Icon   Scientific Poster
Ultrarapid Whole Genome Sequencing Facilitates Early Definitive Diagnosis of Rare Genetic Disorders
This comprehensive ultrarapid whole genome sequencing helped to identify different disorders including metabolic and rare disorders indicating importance of this test as first -tier diagnostic test. With a streamlined assay workflow turnaround time reduced to 5 to 8 days urWGS is highly suitable test for pediatric disorders as well as other rare genetic disorder and ultimately helps in early selection of any possible treatment options and better disease management
Poster Icon   Scientific Poster
Whole Genome Sequencing as a Screening Tool in Healthy Population: Lesson learned from 110 cases
WGS screening test can be considered as new standard of care along with NBS and carrier status prior to family planning , risk of medically actionable conditions , medically actionable conditions, making suitable prophylactic plans, finding medical management guidelines, selecting optimal dosage of medications and adapting to a healthy life style.
Poster Icon   Scientific Poster
Case Presentation: Co-segregation of a Rare GLA Variant of Uncertain Significance within Two Multiplex Families Facilitates Variant Reclassification to Pathogenic
Co-segregation of the variant with disease in two multiplex families provides powerful evidence for its pathogenicity. These families offer seven documented cases of the variant in affected individuals, crucial for its reclassification as pathogenic. Inclusion of patient phenotypes, family history, and clinic notes aids in VOUS resolution timeline. Accurate variant classification provides confirmed genetic diagnosis and access to specialized medical care for these families.
Poster Icon   Scientific Poster
Unveiling Noncoding DMD Variants: Synergizing RNA Sequencing and DNA Sequencing for Enhanced Molecular Diagnosis
This poster demonstrate RNA sequencing as a powerful tool, especially when integrating with DNA sequencing, for elucidating the pathogenicity of DMD variants, achieving a precise genetic diagnosis, and guiding the potential treatments in patients with clinical and pathological suspicions of DMD/BMD without definitive diagnoses after routine genetic testing.
Publication Icon   Literature - Publication Review
Literature review on protein-protein interaction assays for virology research
This literature review reviews recent publications and show the homogeneous assay set-ups used in a variety of different studies. We present the outcomes of each study and how the information gathered could lead to antiviral therapies.
Whitepaper Icon   Whitepaper
Download your white paper on data analysis methods
This white paper gives you tools for analyzing obtained experimental data such as 2nd messenger quantification for GPCR investigation and screening.
Publication Icon   Literature - Publication Review
Novel drugs for cancer therapy development with PROTAC
A review of current homogeneous assay applications for PROTACs
Datasheet Icon   Datasheet
Bead Ruptor VesselVue Homogenizer Datasheet
The Bead Rupture™ VesselVue™ Homogenizer is the device used to activate VesselVue P-formulation microbubble contrast agent for enhanced ultrasound imaging.
Flyer Icon   Flyer
Vanadis NIPT system - Flyer for Patients
Explains the fundamentals of Vanadis NIPT, including how the test works, the conditions tested, the time it can be performed, and the benefits of the screening test.
Flyer Icon   Flyer
Newborn Sequencing Research - Flyer
Communicates the key strengths and components of our newborn sequencing workflow. Built for flexibility, discover our end-to-end sequencing workflow – all offered from one partner.
Brochure Icon   Brochure
Vanadis NIPT system - Brochure for Laboratories
Outlines differentiating features of the Vanadis NIPT system, inclusive of minimal hands-on time, walkaway automation, high precision and no PCR or sequencing. Empowering any laboratory to conduct NIPT in-house.
Brochure Icon   Brochure
Vanadis cfDNA platform - Brochure for Laboratories
Highlights the defining features behind the Vanadis cfDNA platform, including its ease of use, full automation, high precision and no PCR or sequencing required. Now any lab can conduct cfDNA analysis in-house.
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