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Additional file 3 of Comparative transcriptomics analysis revealing flower trichome development during flower development in two Lonicera japonica Thunb. cultivars using RNA-seq

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DataCite Commons2024-02-08 更新2024-07-28 收录
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Additional file 3: Table S1. Comparison of the density of glandular and non-glandular hairs in ‘Damaohua’ and ‘Yujin 1’ (mm-2). Table S2. Comparison of the lengths of glandular and non-glandular hairs in ‘Damaohua’ and ‘Yujin 1’ (μm). Table S3. Assembly summary of transcriptomic data. Table S4. Preprocessing results of sequencing data quality. Table S5. Annotation results of the unigenes. Table S6. Summary of top 10 GO terms and top 20 KEGG pathway assignments for the L. japonica flower transcriptome. Table S7. DEGs involved in trichome development. Table S8. Primers used for analysis of gene expression by qRT-PCR. Table S9. DEGs involved in signal transduction. Table S10. DEGs involved in secondary metabolites. Table S11. DEGs involved in plant resistance.

附加文件3:表S1。‘大毛花’与‘玉津1号’的腺毛与非腺毛密度对比(单位:mm⁻²)。表S2:‘大毛花’与‘玉津1号’的腺毛与非腺毛长度对比(单位:μm)。表S3:转录组数据组装结果汇总。表S4:测序数据质量预处理结果。表S5:单基因簇(unigene)注释结果。表S6:金银花(Lonicera japonica,L. japonica)花转录组的前10条基因本体(Gene Ontology,GO)条目与前20条京都基因与基因组百科全书(Kyoto Encyclopedia of Genes and Genomes,KEGG)通路注释汇总。表S7:参与表皮毛发育的差异表达基因(Differentially Expressed Genes,DEGs)。表S8:实时定量逆转录PCR(qRT-PCR)基因表达分析所用引物。表S9:参与信号转导的差异表达基因。表S10:参与次生代谢产物的差异表达基因。表S11:参与植物抗性的差异表达基因。
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figshare
创建时间:
2020-07-18
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