Summary of consensus sequences is saved in the $output/consensus-summary.txt as a table, with columns give the following stats about each consensus:
Table 1 Summary of consensus sequences from test run.
| subread name | nBase | nPalin | nRemoved | mPalin | mPercent | mPhred | |------------------------------|-------|--------|---------|---------|----------|------| | m54215_191216_174243/4260227 | 1162 | 6 | 0 | 4.25 | 92.92 | 2.89 | | m54215_191216_174243/4325960 | 2635 | 8 | 0 | 7.22 | 93.01 | 5.17 | | m54215_191216_174243/4522859 | 887 | 26 | 12 | 13.64 | 90.98 | 9.5 | | m54215_200221_110350/4784809 | 2643 | 12 | 0 | 11.16 | 94 | 8.3 | | m54215_200221_110350/4980913 | 2508 | 3 | 1 | 2 | 97.43 | 1.22 | | m54215_200221_110350/4981702 | 718 | 17 | 3 | 13.51 | 92.79 | 9.84 |
Consensus sequencing meeting all of the following criteria are likely to have accuracy around 99.%. We recommend to use these sequences for de novo assembly, linkage analysis, low depth variant calling, and similar challenging tasks.
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