Hello everyone,
Hope you having a fine day!
I have recently got interested into NGS and its applications for studying cancer genomes. My group is interested in studying somatic mutation landscape of a particular tumor. After going through some literature and considering my current funding, I have decided to pursue exome sequencing.
The question for which I am or will be using exome sequencing is to see if there is any co-relation between the mutations harbored in the cancer exome and the cancer progression..
Do you think 5 tumor samples will be a good number to start with? We will be using Illumina genome analyzer IIx, PE 58 bp...
Hope you having a fine day!
I have recently got interested into NGS and its applications for studying cancer genomes. My group is interested in studying somatic mutation landscape of a particular tumor. After going through some literature and considering my current funding, I have decided to pursue exome sequencing.
The question for which I am or will be using exome sequencing is to see if there is any co-relation between the mutations harbored in the cancer exome and the cancer progression..
Do you think 5 tumor samples will be a good number to start with? We will be using Illumina genome analyzer IIx, PE 58 bp...
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