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          <r:AttributeValue>Department of Immunology, Genetics and Pathology, Uppsala University</r:AttributeValue>
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            <a:FirstGiven>Kimberly</a:FirstGiven>
            <a:LastFamily>Sturk-Andreaggi</a:LastFamily>
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              <r:String>Kimberly Sturk-Andreaggi</r:String>
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    <r:Citation>
      <r:Title>
        <r:String xml:lang="sv">SUPPLEMENTARY MATERIALS for Mitochondrial DNA genome variation in the Swedish population</r:String>
        <r:String xml:lang="en">SUPPLEMENTARY MATERIALS for Mitochondrial DNA genome variation in the Swedish population</r:String>
      </r:Title>
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          <r:URN>urn:ddi:se.researchdata:2024-357.Individual-0:2.0</r:URN>
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          <r:String xml:lang="sv">Uppsala universitet</r:String>
          <r:String xml:lang="en">Uppsala University</r:String>
        </r:PublisherName>
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      <r:Publisher>
        <r:PublisherName>
          <r:String xml:lang="sv">Uppsala universitet</r:String>
          <r:String xml:lang="en">Uppsala University</r:String>
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      <r:PublicationDate>
        <r:SimpleDate>2022-03-28</r:SimpleDate>
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        <r:IdentifierContent>10.57804/mfyp-ea25</r:IdentifierContent>
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    <r:Abstract>
      <r:Content xml:lang="sv">The data consists of:

- Table S1. The haplogroup breakdown for the 934 SweGen haplotypes included in the final mitochondrial genome dataset.

- Figure S1. Graphical description of the average read depths observed in the SweGen dataset.

- Figure S2. The distribution of read depth for the 16,569 positions of the mitochondrial genome 
based on the average observed in a subset of 100 representative SweGen haplotypes.

- Figure S3. The box-and-whisker plot presents the distribution of average variant frequency for each 
coverage classification group.

Datasetet har ursprungligen publicerats i DiVA och flyttades över till SND 2024.</r:Content>
      <r:Content xml:lang="en">The data consists of:

- Table S1. The haplogroup breakdown for the 934 SweGen haplotypes included in the final mitochondrial genome dataset.

- Figure S1. Graphical description of the average read depths observed in the SweGen dataset.

- Figure S2. The distribution of read depth for the 16,569 positions of the mitochondrial genome 
based on the average observed in a subset of 100 representative SweGen haplotypes.

- Figure S3. The box-and-whisker plot presents the distribution of average variant frequency for each 
coverage classification group.

The dataset was originally published in DiVA and moved to SND in 2024.</r:Content>
    </r:Abstract>
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        <r:URN>urn:ddi:se.researchdata:2024-357.TopicalCoverage:2.0</r:URN>
        <r:Subject xml:lang="en" controlledVocabularyID="10609" controlledVocabularyName="Standard för svensk indelning av forskningsämnen 2025">Genetics and Genomics</r:Subject>
        <r:Subject xml:lang="sv" controlledVocabularyID="10609" controlledVocabularyName="Standard för svensk indelning av forskningsämnen 2025">Genetik och genomik</r:Subject>
        <r:Subject xml:lang="en" controlledVocabularyID="30501" controlledVocabularyName="Standard för svensk indelning av forskningsämnen 2025">Forensic Science</r:Subject>
        <r:Subject xml:lang="sv" controlledVocabularyID="30501" controlledVocabularyName="Standard för svensk indelning av forskningsämnen 2025">Rättsmedicin</r:Subject>
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