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We next ensured that the locations of the SNPs were correct by aligning SNP probe sequences to the human genome reference (GRCh37) using BWA v0.7.5a-r405 (Li and Durbin, 2009).
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Results were corrected by 5% Bonferroni correction.
Scan inhomogeneities were corrected by a shading correction algorithm (14).
These effects were corrected by using advanced ATR correction.
Residual stenoses were corrected by PTA.
The data were corrected by the cell area parameter.
All tests were corrected by the Bonferroni method [29, 30].
Mortality data were corrected by Abbott's formula (Abbott 1925).
The hysteresis loops were corrected by subtracting diamagnetic/paramagnetic slopes.
Element peak intensities were corrected by Scofield factors (Scofield 1976).
Most detected omissions were corrected by the following day.
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