Cofactor Genomics is so much more than a resource for sequencing. We provide real solutions that generate results to make a real difference in your research.
What makes Cofactor tick is the people behind the service. We offer the perfect solution for your sequencing needs so you get the most out of your experiments.
Cofactor Genomics offers the absolute best value in genomic sequencing today. That's because of our unique ability to deliver more than just sequencing.
At Cofactor, we make it as easy as possible to submit your samples. It is our goal to streamline your experiment in the most efficient manner possible.
Learn about Cofactor's web-based analysis and visualization software.
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Cofactor Genomics's robust RNA-seq pipeline provides researchers with the ability to evaluate differential gene expression in their chosen organism. ActiveSite, our intuitive web-based user-interface, enables researchers to examine, sort, and discover patterns in their data that may not be visible when working with text files or in classical expression applications. Our Project Scientists ensure that experiments survey transcriptomes at the appropriate depth. Whether a wide-overview or a deep interrogation, researchers will have confidence in the results we provide.
Cofactor compares every sample against every other sample in a pair-wise fashion. This approach helps delineate and tier data outputs based on comparisons between replicate samples.
Cofactor delivers the FASTA sequence of every cluster of read alignments. This deliverable will closely represent the transcriptome assembly for the given sample.
Cofactor's saturation analysis offers the ability to determine, during the experimental design, the appropriate number of reads to generate for each sample. Using a proprietary saturation pipeline, Cofactor can graph the interaction of reads totals and unique transcript counts. When a transcriptome pool is sequenced to saturation, the resulting saturation curve will be asymptotic. This unique analysis allows us to determine the point where the most data is generated per dollar spent.
Reads that do not align to the reference assembly may be important or interesting in the context of an RNA-seq experiment. We are able to assemble just the unaligned reads which may provide further clues to the etiology of a condition or contamination in a sample.
Cofactor's ActiveSite Viewer is a web portal that hosts all of the information associated with a project. ActiveSite enables clients to examine, sort, and discover patterns in their data that may not be visible when working with just text files or in classical expression applications. Using the viewer, clients are also able to download the background files used to build their analysis.