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            <gco:CharacterString>Coccolithophore culturing, harvesting, and protein extraction - Haploid and diploid cultures of C. braarudii were cultured at 15 degrees celsius and harvested during mid-exponential growth. Proteins were extracted using RIPA buffer and liquid nitrogen grinding.
          Coccolithophore protein mass spectrometry (MS) - TMT labelling, Liquid Chromatography Mass Spectrometry and subsequent raw data analysis were carried out by the Proteomics Facility of Bristol University, UK.
          The raw data files were processed and quantified using Proteome Discoverer software v2.1 (Thermo Scientific) and searched against the latest release version 2021_2 of the C. braarudii predicted protein database (25204 proteins) from Uniprot (www.uniprot.org), and a common contaminates database using the SEQUEST HT algorithm.
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          Differential abundance between life phases was assessed using LIMMA (Ritchie et al., 2015), with a significance level of  less than 0.05.
          Notes on the data spreadsheet -  Accession: Uniprot Accession Number for Coccolithus braarudii
          logFC, AveExpr, t, P.Value, adj.P.Val, B - For information on analysing RNAseq or protein MS data, see package LIMMA: https://kasperdanielhansen.github.io/genbioconductor/html/limma.html
          Unique Peptides - Number of unique peptide for each protein
          Protein FDR Confidence: False discovery rate (FDR), 5  percent = Medium, 1 percent = High
          Blast2GO - Protein annotation
          Description - Protein description from Uniprot
          Best BLAST hit and e value: NCBI Blast hit with highest e-value</gco:CharacterString>
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