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Fig. 1 | BMC Genomics

Fig. 1

From: Transcriptomic landscape of posterior regeneration in the annelid Platynereis dumerilii

Fig. 1

Quality control metrics for Platynereis dumerilii transcriptomes A) Total number of transcripts (left), mean transcript length (middle left), number of transcripts with length above 1000bp (middle right) and above 10 000 bp (right) are shown. All transcriptomes are represented, including our intermediate assemblies (Hybrid 1, Hybrid 2 and Blastema), the two from the literature (Head and Embryonic), and our Reference assembly. B Mean alignment rate (percentage of reads mapped) for each transcriptome assembly. Reads from the Blastema, the Embryonic and the Head datasets (see Additional file 2) were mapped on the six transcriptomes with bowtie2 [54]. C BUSCO completeness metrics for the Embryonic, the Head, and our Reference transcriptomes. Complete single-copy and complete duplicated were merged because of the redundancy that is normally occurring in de novo transcriptome assemblies. D Swiss-Prot BLASTX results for each transcriptome assembly. Total bar height represents total number of transcripts with a significant BLASTX hit (e-value cutoff 10-5), colored bars represent the number of transcripts having the indicated coverage with a Swiss-Prot sequence. All BLASTX were done on the non-redundant Swiss-Prot database

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