Table 3. Number of SNPs and false positive variants detected, after alignments of untrimmed reads.
Sequencing technology | Alignments | True variants >20% | False positives>20% | True variants >10%* | False positives>10%* |
Roche 454 | Full length reads | 48 | 4 | 49 | 15 |
Trimmed reads | 46 | 1 | 47 | 6 | |
Illumina GA | Full length reads | 49 | 0 | 52 | 1 |
Trimmed reads | 49 | 0 | 52 | 1 | |
ABI SOLiD | Full length reads | 48 | 0 | 51 | 0 |
Trimmed reads | 50 | 0 | 51 | 0 |
*Values inclusive of the elements detected with a >20% threshold.