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        <parTitl xml:lang="en">Activating mutations remodeled the chromatin accessibility landscape to drive distinct regulatory networks in KMT2A-rearranged acute leukemia associated with immune evasion</parTitl>
        <IDNo agency="SND">doi-10-17044-scilifelab-24260710-0</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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        <parTitl xml:lang="en">Activating mutations remodeled the chromatin accessibility landscape to drive distinct regulatory networks in KMT2A-rearranged acute leukemia associated with immune evasion</parTitl>
        <IDNo agency="SND">doi-10-17044-scilifelab-24260710-0</IDNo>
        <IDNo agency="DOI">https://doi.org/10.17044/SCILIFELAB.24260710</IDNo>
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        <AuthEnty xml:lang="en" affiliation="Science for Life Laboratory">Pilheden, Mattias</AuthEnty>
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        <distrbtr xml:lang="en" abbr="SND" URI="https://snd.se">Swedish National Data Service</distrbtr>
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        <distDate xml:lang="en" date="2023-11-24" />
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      <abstract xml:lang="en" contentType="abstract">This dataset includes ATAC-seq (Assay for Transposase-Accessible Chromatin using sequencing) of five infants with acute lymphoblastic leukemia. All patients had an underlying rearrangement of the KMT2A genes, either KMT2A::MLLT1 (n=1), KMT2A::AFF1 (n=3), or KMT2A::MLLT10 (n=1). Three patients also had activating mutations of NRAS G13D and/or KRAS G12D. The median age of the cohort was 2 months 7 days. Diagnostic sample from bone marrow underwent the ATAC-seq library preparation and sequenced on the NextSeq 500 platform (Illumina, San Diego, CA, USA).</abstract>
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