Fig. 5From: A simple procedure for directly obtaining haplotype sequences of diploid genomesCoverage at SNP loci in bulk genomic DNA data plotted against the number of subcellular libraries in which heterozygotes were found. The strong correlation between depth of coverage in the bulk genomic DNA sample and number of heterozygote containing subcell libraries (r2 = 0.84) suggests that increasing copy number causes more libraries to contain contigs representing that regionBack to article page