Outcomes
1
Single integrated system for germline variant detection
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Detects SNV, CNV and de novo variants
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Hours from fastq to annotated and prioritised variants
Overview
Genetic tests such as sequencing generated gigabytes of data from a single individual sample. To harness the power of data analytics, we have developed a fully automated data analysis and interpretation software for germline sequencing data.
Powered by artificial intelligence, the Decipher WES data analysis suite is ideal for individuals who want to gain deep insights into their germline targeted panel and whole exome data. Albeit, without the need to write a single line of code!
3 Big Takeaways
One click, all analysis done
Our unified and simple to use interface requires minimal training and minimal input. Simply upload your data, and let the software do its magic! Our proprietary suite of software will analyse your Fastq file and return results in the form of annotated, prioritised and scored list of SNV, CNV and de novo variants, whilst leveraging phenotype data coded in HPO format.
No requirement of expensive hardware
We understand the expense of developing cutting edge hardware infrastructure required to carry out complex genomic analyses. Hence, we took it upon ourselves to develop the same so that you can carry out your analysis worry-free. All you need is a PC or a laptop with an internet connection!
Data security
We understand that security of data is of utmost priority. To ensure data protection, we have developed a multi-layered security protocol to ensure your data is protected with the industry leading security safeguards. We are HIPAA and ISO 27000 compliant.