An unannotated version of the trascriptome assembly (contigs and unigenes) is presented here.

An unannotated version of the trascriptome assembly (contigs and unigenes) is presented here.

An unannotated version of the trascriptome assembly (contigs and unigenes) is presented here.

The raw reads were used to generate a de novo assembly. High quality reads were then assembled into contigs and tese contigs were then further assembled into unigenes using paired end information to combine contigs that arose from the same transcript.

All unigenes were screened against protein databases Nr, SwissProt, KEGG and COG using BLASTx (e-value<10-5) and against nucleotide database Nt using BLASTn (e-value<10-5). The best hits were used to determine the sequence direction of the unigenes.