<?xml version='1.0' encoding='utf-8'?>
<?xml-stylesheet type="text/xsl" href="/v2/static/oai2.xsl"?>
<OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd">
  <responseDate>2026-10-07T23:53:59Z</responseDate>
  <request identifier="oai:figshare.com:article/31292941" metadataPrefix="oai_dc" verb="GetRecord">https://api.figshare.com/v2/oai</request>
  <GetRecord>
    <record>
      <header>
        <identifier>oai:figshare.com:article/31292941</identifier>
        <datestamp>2026-09-28T09:19:58Z</datestamp>
        <setSpec>category_24295</setSpec>
        <setSpec>category_24784</setSpec>
        <setSpec>item_type_3</setSpec>
        <setSpec>month_year_09_2026</setSpec>
      </header>
      <metadata>
        <oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"  xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
          <dc:title>CyTOF analysis for A549 cell lines (4 LOY and 2 ROY)</dc:title>
          <dc:creator>Michael Scherer (12212429)</dc:creator>
          <dc:creator>Kathleen Schlüter (23156971)</dc:creator>
          <dc:creator>Maria Llamazares-Prada (21632297)</dc:creator>
          <dc:creator>Mei Ju Chen (23156976)</dc:creator>
          <dc:creator>Christoph Plass (14946945)</dc:creator>
          <dc:subject>Epigenetics (incl. genome methylation and epigenomics)</dc:subject>
          <dc:subject>Cancer genetics</dc:subject>
          <dc:subject>CyTOF</dc:subject>
          <dc:subject>histone modifcation</dc:subject>
          <dc:subject>epigenomics and epigenetics</dc:subject>
          <dc:description>&lt;p dir="ltr"&gt;CyTOF data underwent the following pre-processing prior to analyses: First, the CyTOF software by Fluidigm was used for normalization and concatenation of the acquired data. Then, several gates were applied using the Cytobank platform (Beckman Coulter):&lt;/p&gt;&lt;p dir="ltr"&gt;First, the normalization beads were gated out using the 140Ce channel. Then, live single cells were gated using the cisplatin 195Pt, iridium DNA label in 193Ir, event length, and the Gaussian parameters of width, center, offset and residual channels. CyTOF software was then used for samples de-barcoding.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-28T09:19:58Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.6084/m9.figshare.31292941.v1</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/CyTOF_analysis_for_A549_cell_lines_4_LOY_and_2_ROY_/31292941</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
        </oai_dc:dc>
      </metadata>
    </record>
  </GetRecord>
</OAI-PMH>
