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. 2014 Oct 23;111(44):E4762–E4768. doi: 10.1073/pnas.1405423111

Fig. 3.

Fig. 3.

IRAK1 haplotypes. In addition to the common SNV, we also uncovered multiple sample-specific SNVs across the IRAK1 coding sequence (cds). These allowed us to establish SVN haplotypes in IRAK1 for each of the samples. Shown are the positions of all SNVs across the IRAK1 targeted regions on the x axis and the sample name on the y axis. Dots indicate a nucleotide difference from the hg19 reference genome, and the color of the dots indicates the number of reads covering that specific SNV on a log10 scale. Note that all nucleotide positions were covered in all cell lines. Note that each cell line has a different SNV pattern, demonstrating the unique origin of each of our samples.