Skip to main content
. 2010 Jan 15;26(5):589–595. doi: 10.1093/bioinformatics/btp698

Table 1.

Evaluation on simulated data

Program Metrics 100 bp
200 bp
500 bp
1000 bp
10 000 bp
2% 5% 10% 2% 5% 10% 2% 5% 10% 2% 5% 10% 2% 5% 10%
BLAT CPU sec 685 577 559 819 538 486 1078 699 512 1315 862 599 2628 1742 710
Q20% 68.7 25.5 3.0 92.0 52.9 7.8 97.1 86.3 21.4 97.7 96.4 39.0 98.4 99.0 94.0
errAln% 0.99 2.48 5.47 0.55 1.72 4.55 0.17 1.12 4.41 0.01 0.52 3.98 0.00 0.00 1.28
BWA-SW CPU sec 165 125 84 222 168 118 249 172 152 234 168 150 158 134 120
Q20% 85.1 62.2 19.8 93.8 88.7 49.7 96.1 95.5 85.1 96.9 96.5 95.0 98.4 98.5 98.1
errAln% 0.01 0.05 0.17 0.00 0.02 0.13 0.00 0.00 0.04 0.00 0.00 0.00 0.00 0.00 0.00
SSAHA2 CPU sec 4872 7962 9345 1932 2236 5252 3311 8213 6863 1554 1583 3113
Q20% 85.5 83.8 78.2 93.4 93.1 91.9 96.6 96.5 96.1 97.7 97.6 97.4
errAln% 0.00 0.01 0.19 0.01 0.00 0.01 0.00 0.01 0.04 0.00 0.00 0.00

Approximately 10 000 000 bp data of different read lengths and error rates are simulated from the human genome. Twenty percent of errors are indel errors with the indel length drawn from a geometric distribution (density: 0.7·0.3l−1). These simulated reads are aligned back to the human genome with BLAT (option -fastMap), BWA-SW and SSAHA2 (option −454 for 100 and 200 bp reads), respectively. The aligned coordinates are then compared with the simulated coordinates to find alignment errors. In each cell in this table, the three numbers are the CPU seconds on a single-core of an Intel E5420 2.5 GHz CPU, percent alignments with mapping quality greater than or equal to 20 (Q20), and percent wrong alignments out of Q20 alignments. SSAHA2 and BWA-SW report mapping quality; BLAT mapping quality is estimated as 250 times the difference of the best and second best alignment scores divided by the best alignment score (essentially the same calculation as the one for BWA-SW).