<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/DRR022/DRR022241/DRR022241_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/DRR022/DRR022241/DRR022241_1.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>Institute of Wood Technology, Akita Prefectural University</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJDB3018</full_dataset_link><scientific_name>Thujopsis dolabrata var. hondae</scientific_name><long_description>A cDNA library was constructed from leaves and cambium with surrounding tissues from a Thujopsis dolabrata var. hondae tree in Japan. After total RNA was extracted from each tissue using a CTAB-based method, each batch of RNA was mixed equal-molarly. cDNA synthesis was carried out using TruSeq RNA Sample Prep Kit (Illumina) by Hokkaido System Science Co., Ltd (Sapporo, Japan). The library was sequenced using HiSeq 1000 (Illumina) with 2?101-bp paired-end reads by Biotechnology Center of Akita Prefectural University (Akita, Japan).</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Thujopsis dolabrata var. hondae</name><description>illumine Hiseq sequencing of cDNA derived from leaf and cambium mRNA</description><dates><last_updated>2025-09-24</last_updated><first_public>2015-02-21</first_public></dates><accession>PRJDB3018</accession><cross_references><taxon>565456</taxon></cross_references></HashMap>