Outlook of the Global Healthcare Analytics Market: Potential Growth, Share,Research, Sales, Trends, Supply, and Forecast from 2017 to 2022: Top Key Vendors:IBM Corporation,SAS Institute,Optum, Inc.,Truven Health Analytics,Cerner Corporation,McKesson Corporation


Outlook of the Global Healthcare Analytics Market: Potential Growth, Share,Research, Sales, Trends, Supply, and Forecast from 2017 to 2022: Top Key Vendors:IBM Corporation,SAS Institute,Optum, Inc.,Truven Health Analytics,Cerner Corporation,McKesson Corporation http://www.military-technologies.net/2017/11/15/outlook-of-the-global-healthcare-analytics-market-potential-growth-shareresearch-sales-trends-supply-and-forecast-from-2017-to-2022-top-key-vendorsibm-corporationsas-instituteoptum-inc-tr/

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What is DNA Sequencing Ask Team Genomics Deerwalkinc Biotech


Genomics Biotech Services What are these?

1. DNA Sequencing Services

DNA sequencing services involve analyzing sequence data of genes linked to cardiology, immunology, ophthalmology, nephrology, pulmonology, urology, gastroenterology, metabolic, hematology, oncology and endocrinology.

Deliverables:

  • Software-based quality analysis of DNA sequencing results (software: SeqScape, Sequence Scanner)
  • Documentation of sequencing results of patients/subjects in Quality Analysis Reports; generation of genetic testing reports
  • Identifying and providing nomenclature of variants, and associating variants with clinical significance scores based on mutational database
  • Identifying and calculating insertion/deletion variants in sequenced genes

2. Variant Science Services

Variant science work includes determining a patient’s variants and evaluating the predisposition of genotype in relation to phenotype.
Processes executed:

  • Curating genetic variants and related information from biomedical journals for use in database applications – Variants are curated and annotated according to Human Genome Variation Society (HGVS) nomenclature. This process includes:
    • Extracting articles that describe variants from online sources such as Scholar Google, Google, Pub Med
    • Reading the articles and manually listing all genetic variants and related information
    • Deriving the standard nomenclature of genetic variants according to HGVS

http://www.deerwalk.com/services/deerwalk-genomics