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    <responseDate>2026-10-15T00:37:20Z</responseDate>
    <request verb="GetRecord" metadataPrefix="oai_dc" identifier="10.57760/sciencedb.15166" >https://www.scidb.cn/oai</request>
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    <header >
    <identifier>10.57760/sciencedb.15166</identifier>
    <datestamp>2025-06-30T10:12:23Z</datestamp>
</header>
    <metadata>
        
<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2025-06-30</dc:date>
  <dc:title>Single-cell transcriptomic and TCR profiling of T-cell lymphoblastic lymphoma</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.15166</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>T-cell lymphoblastic lymphoma (T-LBL) arises from precursor lymphoblastic cells and is often categorized alongside T-cell acute lymphoblastic leukemia (T-ALL), with differentiation primarily based on the proportion of blasts in the bone marrow. There is a current dearth of specific therapeutic strategies for T-LBL, and interventions for relapsed/refractory T-LBL are also lacking. Here we performed single-cell RNA sequencing and single-cell T-cell receptor sequencing on T-LBL samples.Detailed information and references of the dataset, see: Jiali Wang, Yi-Xuan Zhang et al., Clin. Transl. Med. 2025;15:e70380 ( https://doi.org/10.1002/ctm2.70380 )</dc:description>
  <dc:subject>T-LBL; lymphoma; scRNA-seq; TCR</dc:subject>
  <dc:creator>Jiali Wang</dc:creator>
  <dc:creator>Yi-Xuan Zhang</dc:creator>
  <dc:rights>RESTRICTED</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:relation>http://www.doi.org/10.1002/ctm2.7038</dc:relation>
  <dc:publisher>Science Data Bank</dc:publisher>
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