Hi all,
I'm a PhD student from NZ about to delve into next gen sequencing for my project. No one in my group has any idea with what to do but lucky we have a guy in our department who showed me how to get started with Linux (which is the easy bit!). Normally I just do linkage and Sanger sequencing to find my patient's mutations...
I'll probably be extensively using this forum over the next wee while as I figure out how to analyse my data. My PI has also told me he wants me to set up some whole exon capture with Illumina over the next few months. Anyone used Aligent SureSelect and found it good/bad? And is there a good online tute for all this SAM tools Bowtie stuff...?
-Cheers!
I'm a PhD student from NZ about to delve into next gen sequencing for my project. No one in my group has any idea with what to do but lucky we have a guy in our department who showed me how to get started with Linux (which is the easy bit!). Normally I just do linkage and Sanger sequencing to find my patient's mutations...
I'll probably be extensively using this forum over the next wee while as I figure out how to analyse my data. My PI has also told me he wants me to set up some whole exon capture with Illumina over the next few months. Anyone used Aligent SureSelect and found it good/bad? And is there a good online tute for all this SAM tools Bowtie stuff...?
-Cheers!
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