Dear all
My name is Fahmi and I am currently doing my PhD at The Roslin Institute about network-based visualization and usability of user interfaces in NGS Graph Generator (http://seq-graph.roslin.ed.ac.uk/).
As a part of my work, I will be conducting a usability study on the NGS Graph Generator application. I am currently looking for people to take part in this usability study. If you are interested please answer the questionnaire here.
https://goo.gl/forms/g7oysecaTsk6nU6f1
I am looking who have been involved with the splice variation/transcriptome/alternative splicing either using RNA-seq or microarray. You can try it yourself first and follow the tutorial section in NGS Graph Generator website.
Please reply to this post if you are interested and have any questions, please let me know.
Thank you for reading, Fahmi
