Hello all, I have a prelim coming up where I need to present on methods out of my jurisdiction.
I would like to take samples of primary tumor and sequence two well-characterized receptors to look at genetic variation present in them.
How do I prep genomic DNA for sequencing, do I need next-generation sequencing (Illumina machine) or an older method, once I have sequences how do I line them up and look for patterns?
Any advice or direction is appreciated, cheers.
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Sequencing of receptor variants in tumor
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