Hi fellow members,
I would like to get some explanation from those respected seniors who are experienced in the Bioinformatics analyses as i'm a newbie in the Bioinformatics work.
So, the questions are regarding the annovar output:
- what does it denoted by "." in the SNP column of the annovar output?
- is there any website or link or papers that i can refer to interpret the variants data from the annovar output?