Hi,

I am trying to analyze some RNA-seq data using the Galaxy. The reads for each 
sample comes from 3 lanes, so I need to integrate these three lane reads to be 
able to make a comparison between my samples. How do I 'put together' these 
three read-files? Is there any tools available in Galaxy for that, which I have 
missed? Unfortunately I do not have any programming skills.

Many thanks,
Mehdi M
----------------------------------------
Mehdi Motallebipour, PhD
Mammalian Neurogenesis
MRC Clinical Sciences Centre
Imperial College London
Hammersmith Hospital Campus
Du Cane Road
London
W12 0NN
United Kingdom
Tel: +44-20-8383 8285


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