Quickly uncover insights with the most accurate comparative gene dataset assembled anywhere.

CodeXome® empowers genomic researchers with the only dataset painstakingly built to provide complete control over the molecular and bioinformatic processing in every single sample.

Because finding answers to disease can’t wait.

Accelerate Discovery

The proprietary tools in CodeXome® facilitate uncovering the most precise and refined list of biologically meaningful targets assembled anywhere.

Clarify Objectives

CodeXome®’s breakthrough technology cuts through dense, noisy data to let you complete precise genome analysis in record time.

Improve Understanding

With a curated set of results at your fingertips, you can get to work on finding the answers to genomics questions with just a few clicks of your keyboard.

The volume of genetic data is piling up.
Unfortunately, so is the friction.

Biomedicine and wildlife conservation researchers remain frustrated by the months it typically takes to access and compile genomic data.

Once acquired, researchers have to clean and organize a mosaic of datasets from disparate file formats.

The collection of samples were not curated with the goal of illuminating the history of a gene, so gaps and biased content cloud insights.

Most importantly, many of today’s publicly available gene datasets are woefully incomplete.

CodeXome’s database has strategically assembled:

Number of Genera

%

Primate Diversity Represented

Number of Genes

Examine the context of DNA variation across
millions of years of evolution in seconds.

CodeXome® helps researchers quickly and precisely cut through dense, noisy data using revolutionary digital analytical software.

Avoid Tedious Compilation

Step #1 for any genome researcher is to gather the data.

In this case, because the actual biological specimen are near impossible to acquire, that means you start by using publicly available data. That also means that you need to know where to look. It turns out that there is no single easy button to do this, and there are many steps involved to get information for just a single gene. You’d need to repeat this for every gene.

CodeXome® gives you an easy button (it’s actually a search bar) to access every gene at the click of your keyboard.

Avoid Tedious Compilation

Step #1 for any genome researcher is to gather the data.

In this case, because the actual biological specimen are near impossible to acquire, that means you start by using publicly available data. That also means that you need to know where to look.

It turns out that there is no single easy button to do this, and there are many steps involved to get information for just a single gene. You’d need to repeat this for every gene.

We have the easy button (it’s actually a search bar) – to review every gene at the click of your keyboard.

Reveal Variants in Context

Step #2 for the genome researchers is to validate the accuracy of their data in context.

Even though there may be resources that are free to use, you need to act as your own expert curator, and assess the quality and comprehensiveness of the samples in these public datasets.

If you thought Step 1 was challenging, wait until you have to clean and organize a mosaic of datasets in disparate file formats.

With CodeXome®, Cornerstone Genomics built every dataset from the ground up, with complete control over the molecular and bioinformatic processing in every single sample.

Complete Analysis in Record Time

Step #3 is to actually use your hard-earned data.

Thus far, all you have is raw data. If you want to interpret the information, you still need to perform all the analytical tasks.

Public datasets rarely integrate the analytical functions with their own data, leaving researchers with additional leg work to begin making their discoveries (and using potentially incomplete datasets to begin with makes these challenging analyses even more difficult). 

CodeXome® solves that problem with proprietary tools that help you examine the context of DNA variations across millions of years of evolution in seconds.

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As researchers, we know that bleary-eyed people don’t make many discoveries.

That’s why a “Ureka! Moment“ inspired Cornerstone Genomic’s CEO to leave the National Cancer Institute-National Institutes of Health after 20 years of genomic research to build the entirely unique analysis tool called CodeXome®.

Early support comes from the National Science Foundation.