<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kambara K</submitter><funding>Japan Society for the Promotion of Science</funding><pagination>e0286804</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10243633</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(6)</volume><pubmed_abstract>The family Orchidaceae comprises the most species of any monocotyledonous family and has interesting characteristics such as seed germination induced by mycorrhizal fungi and flower morphology that co-adapted with pollinators. In orchid species, genomes have been decoded for only a few horticultural species, and there is little genetic information available. Generally, for species lacking sequenced genomes, gene sequences are predicted by de novo assembly of transcriptome data. Here, we devised a de novo assembly pipeline for transcriptome data from the wild orchid Cypripedium (lady slipper orchid) in Japan by mixing multiple data sets and integrating assemblies to create a more complete and less redundant contig set. Among the assemblies generated by combining various assemblers, Trinity and IDBA-Tran yielded good assembly with higher mapping rates and percentages of BLAST hit contigs and complete BUSCO. Using this contig set as a reference, we analyzed differential gene expression between protocorms grown aseptically or with mycorrhizal fungi to detect gene expressions required for mycorrhizal interaction. A pipeline proposed in this study can construct a highly reliable contig set with little redundancy even when multiple transcriptome data are mixed, and can provide a reference that is adaptable to DEG analysis and other downstream analysis in RNA-seq.</pubmed_abstract><journal>PloS one</journal><pubmed_title>Construction of a de novo assembly pipeline using multiple transcriptome data sets from Cypripedium macranthos (Orchidaceae).</pubmed_title><pmcid>PMC10243633</pmcid><funding_grant_id>JP17K19253</funding_grant_id><pubmed_authors>Fujino K</pubmed_authors><pubmed_authors>Kambara K</pubmed_authors><pubmed_authors>Shimura H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Construction of a de novo assembly pipeline using multiple transcriptome data sets from Cypripedium macranthos (Orchidaceae).</name><description>The family Orchidaceae comprises the most species of any monocotyledonous family and has interesting characteristics such as seed germination induced by mycorrhizal fungi and flower morphology that co-adapted with pollinators. In orchid species, genomes have been decoded for only a few horticultural species, and there is little genetic information available. Generally, for species lacking sequenced genomes, gene sequences are predicted by de novo assembly of transcriptome data. Here, we devised a de novo assembly pipeline for transcriptome data from the wild orchid Cypripedium (lady slipper orchid) in Japan by mixing multiple data sets and integrating assemblies to create a more complete and less redundant contig set. Among the assemblies generated by combining various assemblers, Trinity and IDBA-Tran yielded good assembly with higher mapping rates and percentages of BLAST hit contigs and complete BUSCO. Using this contig set as a reference, we analyzed differential gene expression between protocorms grown aseptically or with mycorrhizal fungi to detect gene expressions required for mycorrhizal interaction. A pipeline proposed in this study can construct a highly reliable contig set with little redundancy even when multiple transcriptome data are mixed, and can provide a reference that is adaptable to DEG analysis and other downstream analysis in RNA-seq.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2026-06-24T03:22:49.775Z</modification><creation>2025-04-06T14:10:55.276Z</creation></dates><accession>S-EPMC10243633</accession><cross_references><pubmed>37279244</pubmed><doi>10.1371/journal.pone.0286804</doi></cross_references></HashMap>