Which platform for genetic interpretation should I choose for my clinic?

Colleagues, hello! We are planning to implement a system for interpreting NGS data in our clinic. We are still at the selection stage. It is very important that it works quickly, supports different data formats (especially FASTQ and VCF), and that we can use it for both single cases and family cases. We want to avoid errors and speed up the analysis. It is also important that doctors can easily understand why the system made such a conclusion. If anyone has experience, please share. What is worth trying?

Comments

  • A couple of months ago, we started using InheriNext® from https://compassbioinfo.com/ , and I am very pleased. Interpretation is done quickly - literally in 5-15 minutes. There is ClinVar support, ACMG rules are built-in. But the most important thing is complete transparency. You can immediately see what evidence influenced the conclusion. This helps explain to doctors or patients where the result came from. We use different report templates for the type of disease. It is convenient that you can connect the whole team — geneticists, doctors, bioinformaticians — and discuss cases together.

  • We also use InheriNext®. I work with hereditary oncologies, and the platform is ideal. You can quickly highlight significant options, and then discuss them with the clinical team. Transparency helps avoid misunderstandings. And what is important — the price is adequate, especially if there is a large data flow.

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