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  <docDscr>
    <citation>
      <titlStmt>
        <titl xml:lang="sv">10X single-cell RNA sequencing of hematopoietic stem and progenitor cells from a dual SF3B1-mutant MDS-RS patient and a healthy donor</titl>
        <parTitl xml:lang="en">10X single-cell RNA sequencing of hematopoietic stem and progenitor cells from a dual SF3B1-mutant MDS-RS patient and a healthy donor</parTitl>
        <IDNo agency="SND">2023-222-1</IDNo>
        <IDNo agency="DOI">https://doi.org/10.48723/tt0e-eq82</IDNo>
      </titlStmt>
      <prodStmt>
        <producer xml:lang="en" abbr="SND">Swedish National Data Service</producer>
        <producer xml:lang="sv" abbr="SND">Svensk nationell datatjänst</producer>
      </prodStmt>
      <holdings URI="https://doi.org/10.48723/tt0e-eq82">Landing page</holdings>
    </citation>
  </docDscr>
  <stdyDscr>
    <citation>
      <titlStmt>
        <titl xml:lang="sv">10X single-cell RNA sequencing of hematopoietic stem and progenitor cells from a dual SF3B1-mutant MDS-RS patient and a healthy donor</titl>
        <parTitl xml:lang="en">10X single-cell RNA sequencing of hematopoietic stem and progenitor cells from a dual SF3B1-mutant MDS-RS patient and a healthy donor</parTitl>
        <IDNo agency="SND">2023-222-1</IDNo>
        <IDNo agency="DOI">https://doi.org/10.48723/tt0e-eq82</IDNo>
        <IDNo agency="DOI">10.1016/j.bneo.2024.100011</IDNo>
      </titlStmt>
      <rspStmt>
        <AuthEnty xml:lang="en" affiliation="Department of Medicine, Huddinge / Center for Hematology and Regenerative Medicine (HERM), Karolinska Institutet">Moura, Pedro Luis</AuthEnty>
        <AuthEnty xml:lang="sv" affiliation="Institutionen för medicin, Huddinge / Centrum för hematologi och regenerativ medicin (HERM), Karolinska Institutet">Moura, Pedro Luis</AuthEnty>
        <AuthEnty xml:lang="en" affiliation="Department of Medicine, Huddinge / Center for Hematology and Regenerative Medicine (HERM), Karolinska Institutet">Hellström-Lindberg, Eva</AuthEnty>
        <AuthEnty xml:lang="sv" affiliation="Institutionen för medicin, Huddinge / Centrum för hematologi och regenerativ medicin (HERM), Karolinska Institutet">Hellström-Lindberg, Eva</AuthEnty>
      </rspStmt>
      <prodStmt>
        <grantNo xml:lang="en" agency="Swedish Cancer Society">19 0200</grantNo>
        <grantNo xml:lang="sv" agency="Cancerfonden">19 0200</grantNo>
        <grantNo xml:lang="en" agency="Knut and Alice Wallenberg Foundation">2017.0359</grantNo>
        <grantNo xml:lang="sv" agency="Knut och Alice Wallenbergs stiftelse">2017.0359</grantNo>
        <grantNo xml:lang="en" agency="Swedish Research Council">2021-01404_VR</grantNo>
        <grantNo xml:lang="sv" agency="Vetenskapsrådet">2021-01404_VR</grantNo>
        <grantNo xml:lang="en" agency="Swedish Cancer Society">21 0340</grantNo>
        <grantNo xml:lang="sv" agency="Cancerfonden">21 0340</grantNo>
      </prodStmt>
      <distStmt>
        <distrbtr xml:lang="en" abbr="SND" URI="https://snd.se">Swedish National Data Service</distrbtr>
        <distrbtr xml:lang="sv" abbr="SND" URI="https://snd.se">Svensk nationell datatjänst</distrbtr>
        <distDate xml:lang="en" date="2024-04-18" />
      </distStmt>
      <verStmt>
        <version elementVersion="1" elementVersionDate="2024-04-18" />
      </verStmt>
      <holdings URI="https://doi.org/10.48723/tt0e-eq82">Landing page</holdings>
    </citation>
    <stdyInfo>
      <subject />
      <abstract xml:lang="en" contentType="abstract">This dataset consists of 10X single-cell RNA sequencing data of bone marrow cells (CD34+ stem cells) obtained from two clinical visits of a dual SF3B1-mutant MDS-RS patient (Patient 1 in the associated publication: visits at 31 months post-diagnosis, with dominant SF3B1 N626D; and at 118 months post-diagnosis, with dominant SF3B1 K666N) and one healthy bone marrow donor. The objective of this data collection was to assess how the hematopoietic stem and progenitor cell compartment of this patient differed over time and as a result of changes in clonal frequency. 
The dataset is appoximately 80.9 GB and has filetypes txt, rds and fastq.</abstract>
      <abstract xml:lang="sv" contentType="abstract">Syftet med denna datainsamling var att bedöma hur det hematopoetiska stam- och progenitorcellsutrymmet hos en patient skiljde sig över tiden och som ett resultat av förändringar i klonal frekvens. Se den engelska beskrivningen för mer information.</abstract>
      <sumDscr>
        <anlyUnit xml:lang="en" unit="Cells">Cells<concept vocab="DDI Analysis Unit" vocabURI="https://vocabularies.cessda.eu/v2/vocabularies/AnalysisUnit/2.1.3?languageVersion=en-2.1.3">Cells</concept></anlyUnit>
        <anlyUnit xml:lang="sv" unit="Celler">Celler<concept vocab="DDI Analysis Unit" vocabURI="https://vocabularies.cessda.eu/v2/vocabularies/AnalysisUnit/2.1.3?languageVersion=sv-2.1.3">Celler</concept></anlyUnit>
        <universe xml:lang="en">Patients with Myelodysplastic neoplasms with ring sideroblasts (MDS-RS) and healthy donors</universe>
        <universe xml:lang="sv">Patienter med myelodysplastisk syndrom med ringsideroblaster (MDS-RS) samt friska donatorer</universe>
        <dataKind xml:lang="en">Numeric</dataKind>
        <dataKind xml:lang="en">Other</dataKind>
      </sumDscr>
    </stdyInfo>
    <method>
      <dataColl>
        <timeMeth xml:lang="en">Time series: Discrete<concept vocab="DDI Time Method" vocabURI="https://vocabularies.cessda.eu/v2/vocabularies/TimeMethod/1.2.3?languageVersion=en-1.2.3">Time series: Discrete</concept></timeMeth>
        <timeMeth xml:lang="sv">Tidsserie: Diskret<concept vocab="DDI Time Method" vocabURI="https://vocabularies.cessda.eu/v2/vocabularies/TimeMethod/1.2.3?languageVersion=sv-1.2.3">Tidsserie: Diskret</concept></timeMeth>
        <sampProc xml:lang="en">The data in this dataset comes from 1 dual SF3B1mt MDS-RS patient and 1 healthy donor. It is part of a study where bone marrow (BM) samples were collected from 2 dual SF3B1mt MDS-RS patients (Patient 1: N626D, K666N; Patient 2: K700E, K666N) evaluated at Karolinska University Hospital, Sweden. Diagnostic procedures were performed according to the European LeukemiaNet recommendation and WHO classification for myeloid neoplasms. Mutational status was evaluated at the clinic through panel sequencing for the most common myeloid mutations. Additional samples were collected from a total of 4 healthy NBM donors for control purposes. All source material was provided with written informed consent for research use, given in accordance with the Declaration of Helsinki, and the study was approved by the Ethics Research Committee at Karolinska Institutet.<concept vocab="DDI Sampling Procedure" vocabURI="https://vocabularies.cessda.eu/v2/vocabularies/SamplingProcedure/2.0.1?languageVersion=en-2.0.1">The data in this dataset comes from 1 dual SF3B1mt MDS-RS patient and 1 healthy donor. It is part of a study where bone marrow (BM) samples were collected from 2 dual SF3B1mt MDS-RS patients (Patient 1: N626D, K666N; Patient 2: K700E, K666N) evaluated at Karolinska University Hospital, Sweden. Diagnostic procedures were performed according to the European LeukemiaNet recommendation and WHO classification for myeloid neoplasms. Mutational status was evaluated at the clinic through panel sequencing for the most common myeloid mutations. Additional samples were collected from a total of 4 healthy NBM donors for control purposes. All source material was provided with written informed consent for research use, given in accordance with the Declaration of Helsinki, and the study was approved by the Ethics Research Committee at Karolinska Institutet.</concept></sampProc>
        <sampProc xml:lang="en">Probability: Simple random<concept vocab="DDI Sampling Procedure" vocabURI="https://vocabularies.cessda.eu/v2/vocabularies/SamplingProcedure/2.0.1?languageVersion=en-2.0.1">Probability: Simple random</concept></sampProc>
        <sampProc xml:lang="sv">Sannolikhetsurval: obundet slumpmässigt urval<concept vocab="DDI Sampling Procedure" vocabURI="https://vocabularies.cessda.eu/v2/vocabularies/SamplingProcedure/2.0.1?languageVersion=sv-2.0.1">Sannolikhetsurval: obundet slumpmässigt urval</concept></sampProc>
        <sampProc xml:lang="en">Non-probability: Availability<concept vocab="DDI Sampling Procedure" vocabURI="https://vocabularies.cessda.eu/v2/vocabularies/SamplingProcedure/2.0.1?languageVersion=en-2.0.1">Non-probability: Availability</concept></sampProc>
        <sampProc xml:lang="sv">Icke-sannolikhetsurval: tillgänglighetsurval<concept vocab="DDI Sampling Procedure" vocabURI="https://vocabularies.cessda.eu/v2/vocabularies/SamplingProcedure/2.0.1?languageVersion=sv-2.0.1">Icke-sannolikhetsurval: tillgänglighetsurval</concept></sampProc>
        <sampProc xml:lang="en">Mixed probability and non-probability<concept vocab="DDI Sampling Procedure" vocabURI="https://vocabularies.cessda.eu/v2/vocabularies/SamplingProcedure/2.0.1?languageVersion=en-2.0.1">Mixed probability and non-probability</concept></sampProc>
        <sampProc xml:lang="sv">Blandat sannolikhets- och icke-sannolikhetsurval<concept vocab="DDI Sampling Procedure" vocabURI="https://vocabularies.cessda.eu/v2/vocabularies/SamplingProcedure/2.0.1?languageVersion=sv-2.0.1">Blandat sannolikhets- och icke-sannolikhetsurval</concept></sampProc>
      </dataColl>
    </method>
    <dataAccs>
      <useStmt>
        <restrctn xml:lang="en">Access to data through SND. Access to data is restricted.</restrctn>
        <restrctn xml:lang="sv">Åtkomst till data via SND. Tillgång till data är begränsad.</restrctn>
        <conditions elementVersion="info:eu-repo-Access-Terms vocabulary">restrictedAccess</conditions>
      </useStmt>
    </dataAccs>
    <othrStdyMat>
      <relPubl>
        <citation>
          <titlStmt>
            <titl xml:lang="sv">Pedro Luis Moura, Yasuhito Nannya, Affaf Aliouat, Isabel Juliana Hofman, Teresa Mortera Blanco, Tetsuichi Yoshizato, Ryunosuke Saiki, Masahiro M Nakagawa, Maria Creignou, Ann-Charlotte Björklund, Gunilla Walldin, Indira Barbosa, Monika Jansson, Francesca Grasso, Edda M Elvarsdottir, Petter S Woll, Sten Eirik W Jacobsen, Seishi Ogawa, Eva Hellström-Lindberg, Competition of dual SF3B1mt clones in MDS-RS is associated with distinct RNA mis-splicing in hematopoietic stem cells,
Blood Neoplasia, 2024,100011, ISSN 2950-3280,
https://doi.org/10.1016/j.bneo.2024.100011.</titl>
            <parTitl xml:lang="en">Pedro Luis Moura, Yasuhito Nannya, Affaf Aliouat, Isabel Juliana Hofman, Teresa Mortera Blanco, Tetsuichi Yoshizato, Ryunosuke Saiki, Masahiro M Nakagawa, Maria Creignou, Ann-Charlotte Björklund, Gunilla Walldin, Indira Barbosa, Monika Jansson, Francesca Grasso, Edda M Elvarsdottir, Petter S Woll, Sten Eirik W Jacobsen, Seishi Ogawa, Eva Hellström-Lindberg, Competition of dual SF3B1mt clones in MDS-RS is associated with distinct RNA mis-splicing in hematopoietic stem cells,
Blood Neoplasia, 2024,100011, ISSN 2950-3280,
https://doi.org/10.1016/j.bneo.2024.100011.</parTitl>
            <IDNo agency="DOI">10.1016/j.bneo.2024.100011</IDNo>
          </titlStmt>
          <distStmt>
            <distDate date="2024">2024</distDate>
          </distStmt>
        </citation>
      </relPubl>
    </othrStdyMat>
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