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        <identifier>oai:researchdata.se:2023-122-1/1</identifier>
        <datestamp>2026-03-19</datestamp>
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        <setSpec>subject:ssif:30112</setSpec>
        <setSpec>subject:ssif:301</setSpec>
        <setSpec>subject:ssif:302</setSpec>
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        <setSpec>principal:slug:karolinska-institutet</setSpec>
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        <oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" 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">
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          <dc:identifier>https://doi.org/10.48723/0f0c-p816</dc:identifier>
          <dc:title xml:lang="en">Smart-seq3 and Smart-seq3xpress single-cell RNA sequencing of bone marrow cells from MDS-RS patients</dc:title>
          <dc:title xml:lang="sv">Smart-seq3 och Smart-seq3xpress singel-cell RNA sekvensering av benmärgsceller från MDS-RS patienter</dc:title>
          <dc:creator>https://orcid.org/0000-0002-0493-5394</dc:creator>
          <dc:creator>https://orcid.org/0000-0002-7839-3743</dc:creator>
          <dc:subject xml:lang="en">Natural Sciences</dc:subject>
          <dc:subject xml:lang="sv">Naturvetenskap</dc:subject>
          <dc:subject xml:lang="en">Biological Sciences</dc:subject>
          <dc:subject xml:lang="sv">Biologi</dc:subject>
          <dc:subject xml:lang="en">Cell Biology</dc:subject>
          <dc:subject xml:lang="sv">Cellbiologi</dc:subject>
          <dc:subject xml:lang="en">Genetics and Genomics</dc:subject>
          <dc:subject xml:lang="sv">Genetik och genomik</dc:subject>
          <dc:subject xml:lang="en">Bioinformatics and Computational Biology</dc:subject>
          <dc:subject xml:lang="sv">Bioinformatik och beräkningsbiologi</dc:subject>
          <dc:subject xml:lang="en">Hematology</dc:subject>
          <dc:subject xml:lang="sv">Hematologi</dc:subject>
          <dc:subject xml:lang="en">Basic Cancer Research</dc:subject>
          <dc:subject xml:lang="sv">Basal cancerforskning</dc:subject>
          <dc:description xml:lang="en">This dataset consists of Smart-seq3 single-cell RNA sequencing data of purified RS from the bone marrow and peripheral blood of 2 MDS-RS patients; and Smart-seq3xpress single-cell RNA sequencing data of FACS-sorted hematopoietic stem cells (HSC), multipotent progenitors (MPP), megakaryocyte-erythroid progenitors (MEP) and erythroblasts from 1 MDS-RS patient. The objective of this data collection was to assess several parameters on how the bone marrow of MDS-RS patients differs from that of healthy donors.

This dataset includes raw sequencing data in .fastq format, processed count matrices and associated pseudonymized metadata.
 
Processing: In brief, cells were sorted into 384-well plates containing 3uL Vapor-Lock (Qiagen) and 0.3uL lysis buffer consisting of 0.125 µM OligodT30VN (5'-Biotin-ACGAGCATCAGCAGCATACGAT30VN-3'; IDT) adjusted to reverse transcription (RT), 0.5mM dNTPs/each adjusted to RT volume, 0.1% Triton X-100, 5% PEG8000 adjusted to RT volume, 0.4u RNase Inhibitor (Takara Bio, 40 U/µL). After cell sorting plates were briefly centrifuged before storage at -80C. Before RT, plates were denatured at 72 degrees for 10 min followed by addition of 0.1 µL of RT mix; 25 mM Tris-HCL pH 8.4 (Fischer Scientific), 30mM NaCl (Ambion), 1 mM GTP (Thermo Fisher Scientific), 2.5 mM MgCl2 (Ambion), 8 mM DTT (Thermo Fisher Scientific), 0.25 U/µl RNase Inhibitor (Takara Bio), 0.75 µM Template Switching Oligo (TSO) (5′-Biotin-AGAGACAGATTGCGCAATGNNNNNNNNWWrGrGrG-3′; IDT) and 2 U/µl of Maxima H Minus reverse transcriptase (Thermo Fisher Scientific). Plates were quickly centrifuged after dispensing to ensure merge of lysis and RT volumes. RT was incubated at 42 °C for 90 minutes, followed by ten cycles of 50 °C for 2 minutes and 42 °C for 2 minutes. After RT, 0.6 µL PCR mix was dispensed to each well containing the following; 1× SeqAmp PCR buffer (Takara Bio), 0.025 U/µl of SeqAmp polymerase (Takara Bio) and 0.5 µM Smartseq3 forward and reverse primer. Plates were quickly spun down before being incubated as follows: 1 minute at 95 °C for initial denaturation, 14 cycles of 10 seconds at 98 °C, 30 seconds at 65 °C and 2–6 minutes at 68 °C. Final elongation was performed for 10 minutes at 72 °C.

The dataset consists of 2 folders: 
- SS3_FACS_PB-BM_RS	
- SS3xpress_FACS_HSC_MPP_MEP_EB

The folder SS3_FACS_PB-BM_RS contains 1 rds file, 3 txt files, and 1 compressed folder (tar.gz) with fastq files.
The folder SS3xpress_FACS_HSC_MPP_MEP_EB contains 1 rds file, 7 txt files, and 2 GNU zipped fastq files.

The documentation file File_list_SS3_SS3xpress.txt contains a full list of the files in the dataset.</dc:description>
          <dc:description xml:lang="sv">Syftet med denna datainsamling var att bedöma flera parametrar om hur benmärgen hos MDS-RS-patienter skiljer sig från den hos friska donatorer. Denna datauppsättning består av Smart-seq3 och Smart-seq3xpress singel-cell RNA sekvensering av benmärgsceller från MDS-RS patienter. Se den engelska beskrivningen för mer information.

Datasetet består av 2 mappar:
- SS3_FACS_PB-BM_RS	
- SS3xpress_FACS_HSC_MPP_MEP_EB

Mappen SS3_FACS_PB-BM_RS innehåller 1 rds-fil, 3 txt-filer och 1 komprimerad mapp (tar.gz) med fastq-filer.
Mappen SS3xpress_FACS_HSC_MPP_MEP_EB innehåller 1 rds fil, 7 txt-filer och 2 GNU-zippade fastq-filer.

Dokumentationsfilen File_list_SS3_SS3xpress.txt innehåller en lista över datasetets alla filer.</dc:description>
          <dc:rights>info:eu-repo/semantics/restrictedAccess</dc:rights>
          <dc:rights>https://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
          <dc:publisher xml:lang="en">Karolinska Institutet</dc:publisher>
          <dc:publisher xml:lang="sv">Karolinska Institutet</dc:publisher>
          <dc:date>2023-10-19T13:52:12.575267Z</dc:date>
          <dc:language>eng</dc:language>
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