Hello,
I am fairly new to analyzing trios data. The study design consists of WGS on an affected proband with a rare clinical presentation. I figured out my filtering pipeline but I am wondering if I should also be looking at phasing. As far as I understand, phasing shouldn't tell me anymore information than my filtering given that I have probands with unique presentations. Am I correct? If not, can you guide me to a place that would describe it in more detail? Thanks!
Certainly, the higher your accuracy of parental haplotype determination, the better your chances of characterizing a mutation as a de novo in the offspring. There's software like DenovoGear & GATK's PhaseByTransmission which do that.