posted on 2024-06-11, 05:22authored byUniversity of Kentucky. USDA-ARS, Forage-Animal Production Research Unit, Lexington, Kentucky, USA., Manohar Chakrabarti, Randy D. Dinkins, Arthur G. Hunt
Red clover plants were grown under greenhouse condition with 16h/8h of light/dark cycle. Leaf, root and flower samples were collected, followed by RNA extraction and RNAseq library preparation. RNAseq libraries were sequenced on Illumina platform. Sequenced reads were used to construct a de novo transcriptome assembly. Assembled transcriptome was used to decipher dynamic tissue-specific gene expression patterns in the forage legume red clover.
It is recommended to cite the accession numbers that are assigned to data submissions, e.g. the GenBank, WGS or SRA accession numbers. If individual BioProjects need to be referenced, state that "The data have been deposited with links to BioProject accession number PRJNA287846 in the NCBI BioProject database (https://www.ncbi.nlm.nih.gov/bioproject/)."