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. 2012 Mar 12;7(3):e32973. doi: 10.1371/journal.pone.0032973

Table 1. Description of the results of the alignments on PN40024 for the different sequenced clones by 454 methodology and for PN115 available sequences.

PN386 PN583 PN777 Mean of 3 clones PN115
% of aligned sequences Alignment Step 1 48.1 42.5 40.2 43.6 57.7
Alignment Step 2 0.9 1.1 1.0 1.0 1.3
Alignment Step 3 12.5 21.7 16.7 16.9 8.0
Total of aligned reads 61.5 65.3 57.9 61.5 67.0
% of unaligned sequences Repeat elements 12.5 13.4 13.90 13.2 12.7
Paralogs 12.0 10.1 13.0 11.7 20.3
Cytoplasmic DNA 4.2 3.6 3.7 3.8
Unknown 8.1 6.8 10.4 8.4
Contamination (other organisms) 0.01 0.01 0.01 0.01
Low quality reads 1.7 0.8 1.4 1.3
Total of unaligned reads 38.5 34.8 42.1 38.4 33.0

Proportion of aligned reads in each steps of the alignment process and proportion of unaligned reads on the reference genome. First alignment step: aligned reads with 95% identity on single loci with reference sequence; Second alignment step: reads aligned in this step are composed by a repeat element (between 50–300 b) which was masked and by a unique sequence (greater than 150 b) which allowed alignment; Third alignment step: reads in this step are aligned on reference sequence with a gap parameter fixed at a minimum.