Figure S11. Gel electrophoresis of 39 primers for real-time PCR with cDNA as template (a and b) and a subset (c and d) primers sets using cDNA as template for qRT-PCR. PCR was performed (d) with one primer pair failed to amplify target in RT-PCR using DNA as template (two columns on the most right side). The numbers on top of each plot (a, b, c and d) indicate the code of primer used for PCR amplification, refer to Supplementary S Table 9 for details of each primer pair. (PDF 870 kb
Figure S2. Electrophoresis of primary PCR products after SSH. M: 100 bp marker; Lanes 1–4: products ...
Table S1. RT-PCR candidate gene information. Candidate gene name, Unique ID, forward (F) and reverse...
Figure S3. Electrophoresis of secondary PCR products after SSH. M: 100 bp marker; Lanes 1–4: product...
Figure S12. Test of differential gene expresssion among selected genes from three gene families (USP...
Table S2. Summary of database matches (specific values) for C. gigantea unigenes. (DOCX 15 kb
Table S3. Database matches (full results) for C. gigantea unigenes. (XLSX 1763 kb
Table S1. Summary of assembled contigs, scaffolds and unigenes properties for the C. gigantea unigen...
Figure S10. Alignment of the conserved RxR and DDxxD motifs and motifs variation among 121 TPS seque...
Figure S9. Conserved motifs in LRR-RLK domain from C. gigantea transcriptome and their consensus seq...
Table S8. Characteristics of the transcriptome assemblies from related conifer species and re-analys...
Figure S1. Assessment of reads by FastQC before quality control. a) Quality of raw-reads per base. T...
Table S7. Functional enrichment analysis of the specific gene families from C. gigantea. The full li...
Figure S2. Assessment of reads using FastQC after quality control. a) Quality of reads per base afte...
Figure S8. Multiple sequence alignment (MSA) of the USPA-like domains of the putative USPA protein. ...
Figure S6. Metabolic pathway of the Terpenoid bakcone biosynthesis for the unigenes identified in C....
Figure S2. Electrophoresis of primary PCR products after SSH. M: 100 bp marker; Lanes 1–4: products ...
Table S1. RT-PCR candidate gene information. Candidate gene name, Unique ID, forward (F) and reverse...
Figure S3. Electrophoresis of secondary PCR products after SSH. M: 100 bp marker; Lanes 1–4: product...
Figure S12. Test of differential gene expresssion among selected genes from three gene families (USP...
Table S2. Summary of database matches (specific values) for C. gigantea unigenes. (DOCX 15 kb
Table S3. Database matches (full results) for C. gigantea unigenes. (XLSX 1763 kb
Table S1. Summary of assembled contigs, scaffolds and unigenes properties for the C. gigantea unigen...
Figure S10. Alignment of the conserved RxR and DDxxD motifs and motifs variation among 121 TPS seque...
Figure S9. Conserved motifs in LRR-RLK domain from C. gigantea transcriptome and their consensus seq...
Table S8. Characteristics of the transcriptome assemblies from related conifer species and re-analys...
Figure S1. Assessment of reads by FastQC before quality control. a) Quality of raw-reads per base. T...
Table S7. Functional enrichment analysis of the specific gene families from C. gigantea. The full li...
Figure S2. Assessment of reads using FastQC after quality control. a) Quality of reads per base afte...
Figure S8. Multiple sequence alignment (MSA) of the USPA-like domains of the putative USPA protein. ...
Figure S6. Metabolic pathway of the Terpenoid bakcone biosynthesis for the unigenes identified in C....
Figure S2. Electrophoresis of primary PCR products after SSH. M: 100 bp marker; Lanes 1–4: products ...
Table S1. RT-PCR candidate gene information. Candidate gene name, Unique ID, forward (F) and reverse...
Figure S3. Electrophoresis of secondary PCR products after SSH. M: 100 bp marker; Lanes 1–4: product...