In addition to a consensus from all reads, also include consensus seqs generated for each haplotype. This allows recovery of CG sites which are specific to a particular haplotype, but which may be missed in the consensus from all reads (which is pure majority rules).
In addition to a consensus from all reads, also include consensus seqs generated for each haplotype. This allows recovery of CG sites which are specific to a particular haplotype, but which may be missed in the consensus from all reads (which is pure majority rules).