Hello SEQanswers!
To introduce myself, I am doing some NGS to try to identify certain disease-causing mutations. I have outsourced the work as do not have direct access to the technology, but I will be doing the bulk of the analysis myself.
While I am waiting for my data to be ready (which, of course, is taking much longer than originally estimated!) I have been practising analysing similar datasets from 1000genomes, using Galaxy.
I'm looking forward to any suggestions and comments!
To introduce myself, I am doing some NGS to try to identify certain disease-causing mutations. I have outsourced the work as do not have direct access to the technology, but I will be doing the bulk of the analysis myself.
While I am waiting for my data to be ready (which, of course, is taking much longer than originally estimated!) I have been practising analysing similar datasets from 1000genomes, using Galaxy.
I'm looking forward to any suggestions and comments!
