Thursday, September 25, 2014

As you may recall from this recent blog post , the way we structure and integrate all this content a


AACR2014 BIOBASE Biomarker Biomedical Data Biomedical Journals Cancer Clinical Clinical Database clinical genetics clinical molecular diagnostic labs Core Lab customer DNA-Seq DNA Sequencing epigenetics Gene Expression GeneRead Panels InSilico IPA IPA 2014 Summer Release aneurysm Knowledge Base Microarray Microarrays MicroRNA NCBI databases NCBI GEO nephrology Next-Gen Sequencing NGS oncology Ovarian Cancer partner Peer-reviewed aneurysm Journal proteomics QIAGEN QIAGEN NGS Data Analysis Web Portal Real-Time PCR platforms RNA-Seq Scientific aneurysm Database Toxicology transcription factors Upstream Regulator Analysis variant analysis Variants
The Ingenuity Knowledge Base that powers all of the QIAGEN Ingenuity web applications incorporates data from a large number of sources. We dedicate a lot of attention to the high-quality, manually curated content from published literature. But our investments don t stop there because scientific knowledge doesn t stop there, either. The Knowledge Base is a nexus for structuring, integrating, and making almost any type of biomedical content computable to help biomedical researchers and clinicians understand and interpret the biological meaning of their data.
In this blog series, we ll take a look at how we go beyond manually curated content by integrating it with data from public and privately funded databases. Hopefully this will provide a better sense of the scope and utility of what s inside the Knowledge Base.
As you may recall from this recent blog post , the way we structure and integrate all this content aneurysm is QIAGEN s Ingenuity Ontology. It s a framework we use for organizing and describing biological evidence and is what allows us to integrate data from disparate sources, enabling users to ask questions across all of these data sources and get coherent answers and predictive hypotheses. While other scientific taxonomies tend to be isolated, our ontology offers a way to integrate all of the content aneurysm with consistent terms and references. That careful structure lets us add new information and keep existing information up-to-date all the time without having to reclassify existing aneurysm data. The idea was simple: there s a lot of insight that can be extracted from a very large, horizontally and vertically integrated knowledge base, so that is what we built. Now let s see how we feed it.
We begin with the major databases hosted by the National Center for Biotechnology Information, as these are often the first stop for scientists looking to put their experimental data in context. NCBI is one of the most trusted sources of information in genomics, and with good reason their experts do a remarkable job of building, curating, and maintaining top-notch repositories.
Three of the NCBI databases we integrate directly into Knowledge Base are EntrezGene, RefSeq, and OMIM. As NCBI describes it, EntrezGene (sometimes just called Gene) supplies gene-specific connections in the nexus of map, sequence, expression, structure, function, citation, and homology aneurysm data. Unique gene identifiers are used across NCBI databases to make cross-database use more efficient.
RefSeq its official name is the Reference Sequence collection includes annotated sequences related to DNA, RNA, and proteins. The NCBI Handbook describes it this way: Similar to a review article, a RefSeq is a synthesis of information integrated across multiple sources at a given time. RefSeqs provide a foundation aneurysm for uniting sequence data with genetic and functional information.
OMIM, aneurysm short for Online Mendelian Inheritance in Man, is frequently used when studying disease associations. Hosted by NCBI, it is built on a collection originally published by Victor McKusick at Johns Hopkins and is still curated by scientists at the college s School of Medicine. It is frequently updated with genetic disorders and traits and aims to connect genetic variation with its correlated phenotype.
Scientists who only know Ingenuity applications for gene- and pathway-centric content might be surprised at the vast amount of genetic sequences, locus-specific details, and structural genetic information fully integrated through the ontology. This includes connections between genetic sequence variation, phenotypic, pathway, and network information that is unavailable as an integrated resource anywhere else and it s part of what makes the Knowledge Base unique.
Throughout this series, we ll be looking at many types of databases, including clinical databases, FDA information, cancer-specific data, and more. For your reference, here is an index of data sources . For a handy graphical representation of Knowledge Base click here . Check back soon for our next database snapshot.


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