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    <responseDate>2026-10-15T17:15:01Z</responseDate>
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                <identifier>oai:data.mendeley.com/s64chwbwzx.1</identifier>
                <datestamp>2026-03-16T22:58:51Z</datestamp>
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            <metadata><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <dc:creator>Mishra, Animesh Anand</dc:creator>
    <dc:title>HILIC metabolomics for intracellular metabolite in Candida albican with or without short chain fatty acids </dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Candida  albicans SC5314 was grown under four conditions: 1) YPD at pH 5.0; 2) YPD with 50 mM acetic acid; 3) YPD with 50 mM propionic acid at pH 5.0; 4) YPD with 50 mM butyric acid at pH 5.0. Cultures were grown for 4 hours at 37C aerbobically with shaking. Cultures were harvested and the intracellular metabolome was extracted for HILIC metabolomics.  There are four replicates per condition. The file contains metabolites name; m/z for the metabolite, retention time for metabnolite, raw peak area in each sample, normalized peak area for each sample, ratio of area under YPD samples/ SCFA treated samples, log2 fold change of YPD samples/SCFA treated samples, p value for the ratio of YPD samples/SCFA treated samples, adjusted p value of YPD samples/SCFA treated samples and VIP score</dc:description>
    <dc:subject>Candida albicans</dc:subject>
    <dc:contributor>Koh, Andrew</dc:contributor>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/s64chwbwzx.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/s64chwbwzx.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
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    <dc:date>2026-03-16T22:58:51Z</dc:date>
    <dc:date>2026-03-18T23:59:59Z</dc:date>
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