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        <parTitl xml:lang="en">RNA-sequencing data from: The AML cellular state space unveils NPM1 immune evasion subtypes with distinct clinical outcomes, and: The complement receptor C3AR constitutes a novel therapeutic target in NPM1-mutated AML</parTitl>
        <IDNo agency="SND">doi-10-17044-scilifelab-21557163-0</IDNo>
        <IDNo agency="DOI">https://doi.org/10.17044/SCILIFELAB.21557163</IDNo>
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        <producer xml:lang="en" abbr="SND">Swedish National Data Service</producer>
        <producer xml:lang="sv" abbr="SND">Svensk nationell datatjänst</producer>
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    <citation>
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        <titl xml:lang="sv"></titl>
        <parTitl xml:lang="en">RNA-sequencing data from: The AML cellular state space unveils NPM1 immune evasion subtypes with distinct clinical outcomes, and: The complement receptor C3AR constitutes a novel therapeutic target in NPM1-mutated AML</parTitl>
        <IDNo agency="SND">doi-10-17044-scilifelab-21557163-0</IDNo>
        <IDNo agency="DOI">https://doi.org/10.17044/SCILIFELAB.21557163</IDNo>
      </titlStmt>
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        <AuthEnty xml:lang="en" affiliation="Science for Life Laboratory">Lilljebjörn, Henrik</AuthEnty>
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        <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="2025-10-07" />
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      <holdings URI="https://doi.org/10.17044/SCILIFELAB.21557163">Landing page</holdings>
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      <abstract xml:lang="en" contentType="abstract">This dataset contains bulk RNA-sequencing (RNA-seq) gene expression data from from 120 AML-samples from the subtypes NPM1 (n=33), AML-MR (n=30), TP53 (n=18), PML::RARA (n=8), CBFB::MYH11 (n=8), AML without class defining mutations (n=8), RUNX1::RUNX1T1 (n=3), KMT2A fusion genes (n=3), AML meeting the criteria for two subtypes (n=2), DEK-NUP214 (n=2), GATA2::MECOM (n=1), and bialleleic CEBPA mutation (n=1). The single cell libraries were constructed from bone marrow (n=102) or peripheral blood (n=18) using the TruSeq RNA Library Prep Kit v2 (Illumina) and sequenced on a NextSeq 500. Reads were aligned against human reference genome hg19 and read counts were determined using RSEM v1.2.30 (https://github.com/deweylab/RSEM) with gencode v19 as gene reference. Data is available as fpkm-values as determined by RSEM. Raw sequencing reads (fastq) are available at the European Genome-Phenome Archive (EGA) under accession ID EGAD50000001576: https://ega-archive.org/datasets/EGAD50000001576.</abstract>
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        <restrctn xml:lang="sv">Åtkomst till data via extern aktör. </restrctn>
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