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. 2022 Apr 29;11:e78981. doi: 10.7554/eLife.78981

Table 3. Nucleotide diversity (π) on SD-Mal and SD+ chromosomes.

π ( ± st. dev.) p-value
Chr. Region SD+ SD-Mal SD+ × f SD-Mal vs. SD+ SD-Mal vs. SD+*f
1 2L Distal to
Sd-RanGAP
1.03E-02 1.03E-02 1.52E-04 0.5727 0.00E + 00
(±3.01E-03) (±3.09E-03) (±4.43E-05)
2 2L Proximal to
Sd-RanGAP
4.44E-03 9.39E-05 6.52E-05 5.84E-90 0.0027
(±2.75E-03) (±1.66E-04) (±4.04E-05)
3 2R In(2R)Mal 8.94E-03 7.97E-05 1.31E-04 0.00E + 00 1.42E-33
(±2.95E-03) (±1.18E-04) (±4.33E-05)
4 2L-2R SD-Mal supergene 6.42E-03 7.98E-05 9.43E-05 0.00E + 00 2.60E-06
(±4.03E-03) (±1.32E-04) (±5.92E-05)

Average nucleotide diversity (π) per site and empirical standard deviation estimated in 10-kb windows along chromosome 2, for SD+, SD-Mal, and SD+ scaled by the estimated frequency of SD-Mal chromosomes (SD+× f, where f = 1.47%). Outside of the linked region (row 1), πSD-Mal ~ πSD+. Inside of the linked region (rows 2–4), πSD-Mal < πSD+; even after scaling πSD+ by the frequency of SD-Mal in the population, πSD-Mal < πSD+× f. Due to non-independence of SNPs in non-recombining regions, we also estimated variance in π based on Charlesworth and Charlesworth, 2010; which is 5.30E-05 for In(2R)Mal and 6.27E-05 for the entire SD-Mal supergene. p-values reported by paired t-test between 10-kb windows.