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            <name>Title</name>
            <description>A name given to the resource</description>
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                <text>Coronavirus</text>
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            <description>An account of the resource</description>
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                <text>Dominio científico: Coronavirus</text>
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    <description>A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.</description>
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      <name>Dublin Core</name>
      <description>The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.</description>
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          <name>Title</name>
          <description>A name given to the resource</description>
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              <text>Barcode identification for single cell genomics</text>
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          <name>Creator</name>
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              <text>Akshay Tambe, Lior Pachter</text>
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          <name>Description</name>
          <description>An account of the resource</description>
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              <text>Abstract Background Single-cell sequencing experiments use short DNA barcode ‘tags’ to identify reads that originate from the same cell. In order to recover single-cell information from such experiments, reads must be grouped based on their barcode tag, a crucial processing step that precedes other computations. However, this step can be difficult due to high rates of mismatch and deletion errors that can afflict barcodes. Results Here we present an approach to identify and error-correct barcodes by traversing the de Bruijn graph of circularized barcode k-mers. Our approach is based on the observation that circularizing a barcode sequence can yield error-free k-mers even when the size of k is large relative to the length of the barcode sequence, a regime which is typical single-cell barcoding applications. This allows for assignment of reads to consensus fingerprints constructed from k-mers. Conclusion We show that for single-cell RNA-Seq circularization improves the recovery of accurate single-cell transcriptome estimates, especially when there are a high number of errors per read. This approach is robust to the type of error (mismatch, insertion, deletion), as well as to the relative abundances of the cells. Sircel, a software package that implements this approach is described and publically available.</text>
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          <name>Date</name>
          <description>A point or period of time associated with an event in the lifecycle of the resource</description>
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              <text>2019</text>
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              <text>single cell, Barcodes, barcode identification, de Bruijn Graph, Circularization, k-mer counting</text>
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          <name>Identifier</name>
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              <text>DOI: 10.1186/s12859-019-2612-0</text>
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          <name>Source</name>
          <description>A related resource from which the described resource is derived</description>
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              <text>BMC Bioinformatics</text>
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          <name>Publisher</name>
          <description>An entity responsible for making the resource available</description>
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              <text>BMC</text>
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          <name>Coverage</name>
          <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
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            <elementText elementTextId="12934">
              <text>Biology (General), Computer applications to medicine. Medical informatics</text>
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          <name>Language</name>
          <description>A language of the resource</description>
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              <text>EN</text>
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