Hello from France

[amandinette]

This is my first post on this forum, just to say "hello" to the SeqAnswers community.

I am an engineer in bioinformatics, working on NGS data in an hospital.
I work on 2 types of projects :
- analysing RNA-Seq data to identify differentially expressed genes and splicing events,
- analysing genome or exome data to identify variants (point mutation as well as "bigger" variations like translocations).

I hope to find solutions to my questions here, and also to be able to help other people, by sharing experience.

Cheers,
Amandinette