Hello & a survey

[Arthur.Z]

Hi everybody,

I am new in next-generation sequencing and have a question for you all:

If you are inclined to use commercially available software package or open-source analysis tools to analyze your NGS data?

I am interested in using target gene deep sequencing to uncover genetics mechanisms for rare/orphan diseases in childhood.

I am wondering if there is anyone in this forum with similar research interests like me?

Thanks
Arthur.Z