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        <datestamp>2026-09-15T17:32:50Z</datestamp>
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          <dc:title>&lt;p&gt;Shared Genes with minimum depth of 20 reads per allele from preliminary analysis.&lt;/p&gt;</dc:title>
          <dc:creator>Tyler Weide (23768517)</dc:creator>
          <dc:creator>James Koltes (3570086)</dc:creator>
          <dc:creator>Juan Steibel (6173768)</dc:creator>
          <dc:creator>Karl Kerns (12397696)</dc:creator>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Genetics</dc:subject>
          <dc:subject>Evolutionary Biology</dc:subject>
          <dc:subject>Environmental Sciences not elsewhere classified</dc:subject>
          <dc:subject>Ecology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Developmental Biology</dc:subject>
          <dc:subject>Cancer</dc:subject>
          <dc:subject>potential phenomic indicator</dc:subject>
          <dc:subject>nuclear genomic control</dc:subject>
          <dc:subject>mitotracker &amp;# 8482</dc:subject>
          <dc:subject>heterozygous baseline populations</dc:subject>
          <dc:subject>epifluorescence microscopy confirmed</dc:subject>
          <dc:subject>concept framework establishes</dc:subject>
          <dc:subject>better characterize gamete</dc:subject>
          <dc:subject>allelic ratio distortion</dc:subject>
          <dc:subject>182 candidate snps</dc:subject>
          <dc:subject>sire allelic segregation</dc:subject>
          <dc:subject>minimum sequencing depth</dc:subject>
          <dc:subject>nuclear allele representation</dc:subject>
          <dc:subject>alleles within ejaculates</dc:subject>
          <dc:subject>sperm subpopulations differing</dc:subject>
          <dc:subject>paired mitochondrial subpopulations</dc:subject>
          <dc:subject>sperm mitochondrial abundance</dc:subject>
          <dc:subject>mitochondrial abundance</dc:subject>
          <dc:subject>random segregation</dc:subject>
          <dc:subject>boar sperm</dc:subject>
          <dc:subject>defined subpopulations</dc:subject>
          <dc:subject>mitochondrial fluorescence</dc:subject>
          <dc:subject>mitochondrial architecture</dc:subject>
          <dc:subject>wide allele</dc:subject>
          <dc:subject>viable cells</dc:subject>
          <dc:subject>throughput marker</dc:subject>
          <dc:subject>three boars</dc:subject>
          <dc:subject>subcellular architecture</dc:subject>
          <dc:subject>structural distinction</dc:subject>
          <dc:subject>sorted fractions</dc:subject>
          <dc:subject>potentially serve</dc:subject>
          <dc:subject>positioning variation</dc:subject>
          <dc:subject>green fluorescence</dc:subject>
          <dc:subject>genome sequencing</dc:subject>
          <dc:subject>functional validation</dc:subject>
          <dc:subject>frequency differences</dc:subject>
          <dc:subject>frequency analysis</dc:subject>
          <dc:subject>findings suggest</dc:subject>
          <dc:subject>final assembly</dc:subject>
          <dc:subject>excluding debris</dc:subject>
          <dc:subject>evaluated relative</dc:subject>
          <dc:subject>developmental history</dc:subject>
          <dc:subject>30 reads</dc:subject>
          <dc:description>&lt;p&gt;List of filtered heterozygous SNPs identified in merged populations and exhibiting allele frequency differences between Low and High mitochondrial fluorescence sperm fractions with a 20 reads per allele filter.&lt;/p&gt; &lt;p&gt;(XLSX)&lt;/p&gt;</dc:description>
          <dc:date>2026-09-15T17:40:48Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.1371/journal.pone.0358219.s006</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/_p_Shared_Genes_with_minimum_depth_of_20_reads_per_allele_from_preliminary_analysis_p_/33810629</dc:relation>
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