hi all, I am trying to conduct exome analysis on NGS exome data. the was sent from the Illumina platform as a sorted bam file.
while referring to some of the "best ways" to analyze exome data, and particularly using GATK it seems that i might have to convert the bam -> sai and then realign and then once again create a bam file.
is there any way to use GATK and just use the sorted bam file as it already aligned and sorted.
new to this analysis so might have missed something, any advice in this area will be very appreciated.
A
BAM files can contain unaligned or aligned reads. The most common form is the latter and I am almost sure that is the type you have. You'll need to familiarize yourself with samtools in order to be sure, though.