Table 1.
Number of sequences | Total length (nt) | |
Sanger sequences for assembly | 34 152 | |
Sanger UTs (≥50 nt) | 8 618 | 5 415 737 |
Consensi | 3 999 | |
Singletons | 4 619 | |
NG contigs (≥100 nt) | 29 751 | 5 594 713 |
Input sequence for hybrid assembly | ||
(Sanger UTs + NG contigs) | 38 369 | |
Hybrid contigs | 23 257 | 8 078 653 |
Consensi | 5 924 | |
Singletons | 17 333 |
Assembly of Sanger sequences and next generation (NG) reads resulted in 8618 unique transcripts (UTs) and 29 751 NG contigs, respectively. The rationale of hybrid assembly (23 257 contigs) was to combine the benefits of Sanger (longer transcript assemblies) and NG (deeper sequence coverage) sequencing methods so that a significantly more comprehensive latex transcriptome could be obtained.