Long-read sequencing technologies have improved significantly since their emergence. Their read lengths, potentially spanning entire transcripts, is advantageous for reconstructing transcriptomes. Exi
Number and percentage of HQR (highly quality reads, see Table 1) from each library mapped to A2 or D5 transcripts assembly.Assessment of read content of the assembly.
Alignment to Ae. aegypti gene models and Ae. albopictus genomic scaffolds by contigs in the De novo assemblies and reference-based re-assemblies with increased number of input read pairs. For De novo
