No need to setup any software or procure any hardware. We take care of it all for you so you can focus
on your research. Need an on-premise solution? We can do that too, reach out and
we can get you more details.
Give us your FASTQ files, and we'll take it from there. Multiple aligners, gene/transcript/exon expression
analysis, variant and rare allele detection, QC analysis, differential expression, tag processing, and more.
Share any aspect of your genomics projects with individuals either inside or outside your organization.
Use comments to dialogue with each other and even annotate particular aspects
of analysis results, allowing interesting finds within large data sets to be easily referenced.
All the analyses include interactive visualization tools of the results that
can handle the scale of large genomic projects. Change thresholds when looking at alignments, compare variants
detected across multiple samples, look at heatmaps of gene expression data at different p-values, etc. - all in
real time with just a click.
Curio uses a proprietary approach to the way it breaks jobs down into smaller parts that can be distributed
across a cluster of machines, allowing you to more quickly experiment by exposing intermediate results
while jobs are still in progress and getting you final results in record time.
We store all of the analysis results in a unique "big data" indexed format that
allows you to ask complex questions of the genome across hundreds of samples, and get answers back in
minutes or seconds. If you want the industry standard formats (BAMs, VCFs, etc.) for other purposes, Curio
can easily provide those to you too.
Ready to Get Started?
Using Curio for the first time is as simple as uploading some FASTQ files and clicking
a few buttons (no need to setup pipelines, build indexes, configure scripts, etc.)
Give us a chance to show you how easy it is to research differently.