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. 2013 Aug 1;208(12):1998–2006. doi: 10.1093/infdis/jit392

Table 3.

Pairwise Correlations Between Mutant Allele Frequency Estimates in Clinical Specimens Generated by Various Methodsa

Sanger Sanger-MLE Pooled gDNA (1) Pooled gDNA (2) Pooled gDNA (3)b Pooled gDNA (4)b Pooled DBS (1) Pooled DBS (2)
Sanger <.0001 .0002 .0001 .2004 .2686 .0008 1
Sanger-MLE 0.9992 .0005 .0003 .2935 .3629 .0017 1
Pooled gDNA (1) 0.9929 0.9902 <.0001 .0126 .0219 <.0001 1
Pooled gDNA (2) 0.9943 0.9916 0.9994 .0130 .0296 <.0001 1
Pooled gDNA (3)b 0.9928 0.9895 0.9995 0.9995 .0056 .0067 1
Pooled gDNA (4)b 0.9904 0.9870 0.9992 0.9989 0.9998 .0011 1
Pooled DBS (1) 0.9880 0.9842 0.9991 0.9983 0.9998 1 1
Pooled DBS (2) 0.6264 0.6503 0.6370 0.6257 0.5482 0.5510 0.6259

Abbreviations: DBS, dried blood spot; gDNA, genomic DNA; MLE, maximum likelihood estimation;

a Numbers in lower half are correlation coefficients between estimates of mutant allele frequencies in dhfr (codons 51, 59, 108, and 164) and dhps (codons 437, 540, and 581); numbers close to 1 indicate a positive correlation, those close to −1 indicate a negative correlation, and those close to 0 indicate no correlation between values in the 2 groups. Correlation coefficients that were significant at P < .05 after Bonferroni correction are bolded and italicized. Numbers in upper half of table are P values for the correlation coefficients. Numbers in parentheses indicate technical replicates of the second-generation sequencing reactions.

b Frequencies are available only for the 4 dhfr loci, because dhps was sequenced in only only 2 replicates.