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        <parTitl xml:lang="en">RNA-Seq data from Ovarian Tumours</parTitl>
        <IDNo agency="SND">doi-10-17044-scilifelab-28342484-0</IDNo>
        <IDNo agency="DOI">https://doi.org/10.17044/SCILIFELAB.28342484</IDNo>
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        <producer xml:lang="en" abbr="SND">Swedish National Data Service</producer>
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        <titl xml:lang="sv"></titl>
        <parTitl xml:lang="en">RNA-Seq data from Ovarian Tumours</parTitl>
        <IDNo agency="SND">doi-10-17044-scilifelab-28342484-0</IDNo>
        <IDNo agency="DOI">https://doi.org/10.17044/SCILIFELAB.28342484</IDNo>
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        <AuthEnty xml:lang="en" affiliation="Science for Life Laboratory">Moskov, Mikaela</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="2025-02-04" />
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      <abstract xml:lang="en" contentType="abstract">The data presented in this item contain sensitive information that cannot be shared openly. Work on depositing the data in FEGA Sweden has been initiated. FEGA Sweden is a national node of the Federated European Genome-phenome Archive (FEGA), which allows data to be shared under controlled access. The datasets in FEGA Sweden are findable through the European Genome-phenome Archive web portal (https://ega-archive.org).

This dataset refers to the raw data used in the preprint "Deep plasma proteomics identifies and validates an eight-protein biomarker panel that separate benign from malignant tumors in ovarian cancer" available on MedRxiv (DOI: 10.1101/2024.10.10.24315232v1)

Data Set Description

Samples: 81 fresh frozen tumor tissue samples, either benign or malignant, from women with suspected ovarian cancer were used for analysis of mRNA expression.

Library Preparation and Sequencing: Sequencing libraries were prepared from 122-194 ng (three samples), 200 ng (seven samples) or 500 ng (71 samples) total RNA using the TruSeq stranded mRNA library preparation kit (cat# 20020595, Illumina Inc.) including polyA-selection. The libraries were then sequenced on a NovaSeq 6000 system (Illumina Inc.) on S4 flowcells with version 1.5 sequencing chemistry on three lanes. Paired-end sequencing of with read lengths of 150 bp was used.

Library preparation and sequencing was performed by the SNP&amp;SEQ Technology platform, SciLifeLab, National Genomics Infrastructure Uppsala, Sweden.</abstract>
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        <restrctn xml:lang="en">Access to data through an external actor. Access to data is restricted.</restrctn>
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