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

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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