What is FishingCNV?

FishingCNV

FishingCNV is a handy, Java-based tool made just for genome researchers. If you're diving into exome sequencing data and need to spot copy number variations, this app has got your back!

What Does FishingCNV Do?

This software supports coverage files created by the Genome Analysis ToolKit. It's super user-friendly and includes features that will make your research smoother. For instance, it helps generate RPKM files right from BAM files, coverage files, or even custom ones.

How It Works

You start by uploading your input file. Then, FishingCNV goes to work! It analyzes your data using a ton of control files and spits out the CNVs (that's copy number variations). So you can easily see what's going on in your samples.

Why Use FishingCNV?

If you're in the field of genomics and need to keep track of these variations, this app really simplifies things. Plus, since its based on Java, it runs smoothly across different systems.

User-Friendly Design

No one wants complicated software that takes ages to learn! FishingCNV is designed with ease in mind so you can focus on what matters most—your research!

In Conclusion

If you're looking for a reliable way to detect copy number variations in your exome sequencing data, give FishingCNV a try. It's built for researchers like you who want results without all the fuss!

How Download Works

Go to the Softpas website, press the 'Downloads' button, and pick the app you want to download and install—easy and fast!