<HashMap><database>biostudies-arrayexpress</database><scores/><additional><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><submitter>Marek Marzec</submitter><instrument_platform>Illumina NovaSeq 6000</instrument_platform><study_type>RNA-seq of coding RNA</study_type><organism>Hordeum vulgare</organism><species>Hordeum vulgare</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15240</full_dataset_link><description>Identification of strigolactone-dependent genes in barley involved in response to cadmium (Cd) and zinc (Zn) treatment. Comparison of two organs (shoot and root) allowed to identification of tissue-specific genes that remain under the control of strigolactones in barley</description><repository>biostudies-arrayexpress</repository><sample_protocol>Nucleic Acid Extraction - Samples were frozen immediately in liquid nitrogen; RNA was isolated using the mirVana miRNA Isolation Kit (Sigma, catalogue number: AM1560).</sample_protocol><sample_protocol>Sequencing - Transcriptome sequencing was conducted by Novogene Co., LTD (Beijing, China).</sample_protocol><sample_protocol>Sample Collection - For RNA-isolation analyses, plant tissue (shoot and root) was collected in four biological replicates, each containing tissue from 4 seedlings.</sample_protocol><sample_protocol>Growth Protocol - For the RNAseq experiment, plants were grown in hydroponic conditions up to 21 days. Six plants were placed in the 1.5 l container filled with ½ Hoagland solution (Hoagland and Dennis, 1938). The medium was replaced every week. Plants were placed in the greenhouse under a 20/18°C day/night, 16/8 photoperiod and 420 μE m−2 s−1 light intensity. After eleven days of growth in control conditions, the containers were divided into variants: control, treated with Cd at a concentration of 5 µM, or treated with Zn at a concentration of 50 µM. The treatment lasted another ten days.</sample_protocol><sample_protocol>Library Construction - Preparation of RNA library was conducted by Novogene Co., LTD (Beijing, China).</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><pubmed_authors>Marek Marzec</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA-seq; comparison of root and shoot transcriptome between WT and strigolactone-insensitive mutant (hvd14.d), barley in response to cadmium (Cd) and zinc (Zn) treatment; three-week-old seedlings</name><description>Identification of strigolactone-dependent genes in barley involved in response to cadmium (Cd) and zinc (Zn) treatment. Comparison of two organs (shoot and root) allowed to identification of tissue-specific genes that remain under the control of strigolactones in barley</description><dates><release>2026-05-31T00:00:00Z</release><modification>2026-05-31T01:01:14.056Z</modification><creation>2025-06-12T13:40:19.987Z</creation></dates><accession>E-MTAB-15240</accession><cross_references><ENA>ERP173420</ENA><Biostudies>E-MTAB-13641</Biostudies><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>