Statement_of_Work.pdf

Statement of Work Subscription for Ingenuity Variant Analysis 350

Scope An Ingenuity Variant Analysis 350 subscription allows access to the Qiagen proprietary curated knowledge base assembled by PhD level scientists that currently has over 5.3 million human phenotype associated findings; access to all common public data repositories, 1000 Genomes, Complete Genomics, Exome Server Project, TCGA, ExAC, and Allele Frequency Community for comparison and narrowing the lists of variants of interest; access to the proprietary data base HGMD and PGMD as part of the product offering; the ability to create and utilize a local data base of findings for interpreting NGS data. The subscription includes data storage and state-of-the-art security.

The subscription for Ingenuity Variant Analysis 350 provides an invaluable tool for the discovery of genes and variants associated with inherited human ocular disease.

Ingenuity variant Analysis 350 will allow us to maintain and analyze large amounts of genomic data from human patients, and link this analysis to well-curated bioinformatic tools and databases.

Product

Product No. Product Name Quantity 830288 Ingenuity Variant Analysis 350 1

Period of Performance Base Year: 09/30/2016 – 09/29/2017 Option Year 1: 09/30/2017 – 09/29/2018 Option Year 2: 09/30/2018 – 09/29/2019 Option Year 3: 09/30/2019 – 09/29/2020

Delivery Location National Institutes of Health National Eye Institute 9000 Rockville Pike Building 6 Room 213 Bethesda, MD 20892

Acquisition Contact Eric D. Chapman Contract Specialist 301-435-3910 eric.chapman@nih.gov mailto:eric.chapman@nih.gov