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. 2014 Mar 12;15(1):188. doi: 10.1186/1471-2164-15-188

Figure 2.

Figure 2

BLAST strategy to identify unique transcripts. Identification of unique transcripts in each individual assembly was performed by reserving contigs from one assembly and pooling all contigs from the remaining assemblies. The contigs from the single assembly were aligned to the pooled contigs. Contigs that fail to align were considered unique to that single assembly. The unique contigs were annotated by aligning to the D. melanogaster transcriptome.