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          <dc:title>&lt;p&gt;Genomic details of genome-wide SNPs with HWD in reliable regions.&lt;/p&gt;</dc:title>
          <dc:creator>Elika Garg (5615168)</dc:creator>
          <dc:creator>Jaffa Romain (24950232)</dc:creator>
          <dc:creator>Lei Sun (45752)</dc:creator>
          <dc:creator>Andrew D. Paterson (7588598)</dc:creator>
          <dc:subject>Genetics</dc:subject>
          <dc:subject>Evolutionary Biology</dc:subject>
          <dc:subject>Ecology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Marine Biology</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>order omnibus meta</dc:subject>
          <dc:subject>1000 genomes project</dc:subject>
          <dc:subject>wide significance threshold</dc:subject>
          <dc:subject>poor sequence quality</dc:subject>
          <dc:subject>numerous autosomal loci</dc:subject>
          <dc:subject>hwd ), followed</dc:subject>
          <dc:subject>genomic features indicative</dc:subject>
          <dc:subject>eight snps within</dc:subject>
          <dc:subject>minor allele frequency</dc:subject>
          <dc:subject>hardy &amp;# 8211</dc:subject>
          <dc:subject>sex chromosome sequences</dc:subject>
          <dc:subject>sequence features</dc:subject>
          <dc:subject>autosomal snps</dc:subject>
          <dc:subject>hwd based</dc:subject>
          <dc:subject>chromosome 14q31</dc:subject>
          <dc:subject>&amp;# 8805</dc:subject>
          <dc:subject>allelic snps</dc:subject>
          <dc:subject>wide sex</dc:subject>
          <dc:subject>weinberg equilibrium</dc:subject>
          <dc:subject>weinberg disequilibrium</dc:subject>
          <dc:subject>usually implemented</dc:subject>
          <dc:subject>practical tool</dc:subject>
          <dc:subject>multivariate predictor</dc:subject>
          <dc:subject>missing genotypes</dc:subject>
          <dc:subject>five super</dc:subject>
          <dc:subject>bp region</dc:subject>
          <dc:subject>based selection</dc:subject>
          <dc:subject>based framework</dc:subject>
          <dc:subject>assessing hardy</dc:subject>
          <dc:subject>also interfere</dc:subject>
          <dc:subject>african super</dc:subject>
          <dc:subject>afr ).</dc:subject>
          <dc:subject>active recruitment</dc:subject>
          <dc:subject>490 individuals</dc:subject>
          <dc:description>&lt;p&gt;255 SNPs on autosomes and 1 on NPR with significant HWD were found in reliable regions. Their coordinates were lifted over to GRCh38 for functional annotations from dbSNP and Ensembl VEP (see Methods). An additional annotation indicates their QC status from the original work [&lt;a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1012280#pgen.1012280.ref002" target="_blank"&gt;2&lt;/a&gt;].&lt;/p&gt; &lt;p&gt;(XLSX)&lt;/p&gt;</dc:description>
          <dc:date>2026-09-15T17:43:50Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.1371/journal.pgen.1012280.s022</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/_p_Genomic_details_of_genome-wide_SNPs_with_HWD_in_reliable_regions_p_/33814668</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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