RNA sequencing data from patients with heart disease and controls
SND-ID: 2023-80-1. Version: 1. DOI: https://doi.org/10.5878/e48r-gn02
Citation
Creator/Principal investigator(s)
Victoria Rotter Sopasakis - University of Gothenburg, Department of Laboratory Medicine, Institute of Biomedicine
Lillemor Mattsson Hultén - University of Gothenburg, Department of Laboratory Medicine, Institute of Biomedicine
Research principal
University of Gothenburg - Department of Laboratory Medicine, Institute of Biomedicine
Description
RNA sequencing analysis of atrial cardiac tissue from patients undergoing coronary artery bypass grafting (CABG) or aortic valve replacement (AVR) was performed and compared with atrial cardiac tissue from organ donors and purchased human atrial cardiac RNA.
RNA sequencing analysis was performed at the Genomics Core Facility
at University of Gothenburg, Sweden. All samples (ten controls,
ten CABG patients and ten AVR patients) were quality checked by the
RNA integrity number (RIN) using Tapestation 2200 RNA screenTape
(Agilent Technologies, Santa Clara, CA) and RNA concentration was
measured by NanoDrop (Thermo Fisher, Waltham, MA). RIN values
ranged between 6.6 and 9.0 for all samples. TruSeq Total Stranded RNA
kit with RiboZero (Gold) Sample Preparation Guide (15,031,048 Rev. E)
RNA sequencing analysis was performed at the Genomics Core Facility
at University of Gothenburg, Sweden. All samples (ten controls,
ten CABG patients and ten AVR patients) were quality checked by the
RNA integrity number (RIN) using Tapestation 2200 RNA screenTape
(Agilent Technologies, Santa Clara, CA) and RNA concentration was
measured by NanoDrop (Thermo Fisher, Waltham, MA). RIN values
ranged between 6.6 and 9.0 for all samples. TruSeq Total Stranded RNA
kit with RiboZero (Gold) Sample Preparation Guide (15,031,048 Rev. E)
was used for RNA sample preparation (Illumina, San Diego, CA).
A total of 10 μl (~1 μg) RNA from each sample was used for library
preparation. Directly after depletion, a cleanup step was performed
using 110 ul of the RNAClean XP beads (Beckman Coulter, USA) for each
sample. The fragmentation step was performed for 8 min. 12 PCR cycles
were run for all samples.
Libraries were quantified and normalized with Qubit DNA HS Assay
kit (Life Technologies, Carlsbad, CA) and fragment size determined by
Tapestation 2200 (Agilent Technologies, Santa Clara, CA). The libraries
were pooled together by using the Illumina protocol for pooling and
sequenced with NovaSeq 6000 S1 (Illumina, San Diego, CA) for the read
length of 2 × 100 bp. Show less..
Data contains personal data
Yes
Sensitive personal data
Yes
Type of personal data
Pseudonymized human data (RNA)
Code key exists
Yes
Unit of analysis
Population
Patients undergoing coronary artery bypass grafting (CABG) or aortic valve replacement (AVR) (experimental group) and organ donors and purchased human RNA (control group).
Study design
Experimental study
Preclinical study
Sampling procedure
Data format / data structure
Geographic spread
Geographic location: Sweden
Responsible department/unit
Department of Laboratory Medicine, Institute of Biomedicine
Ethics Review
Gothenburg - Ref. 560-12 and 436-15
Research area
Biochemistry and molecular biology (Standard för svensk indelning av forskningsämnen 2011)
Genetics (Standard för svensk indelning av forskningsämnen 2011)
Bioinformatics and systems biology (Standard för svensk indelning av forskningsämnen 2011)
Basic medicine (Standard för svensk indelning av forskningsämnen 2011)
Medical genetics (Standard för svensk indelning av forskningsämnen 2011)
Cell and molecular biology (Standard för svensk indelning av forskningsämnen 2011)
Cardiac and cardiovascular systems (Standard för svensk indelning av forskningsämnen 2011)
Joakim Sandstedt, Kristina Vukusic, Elham Rekabdar, Göran Dellgren, Anders Jeppsson, Lillemor Mattsson Hultén, Victoria Rotter Sopasakis. Markedly reduced myocardial expression of γ-protocadherins and long non-coding RNAs in patients with heart disease. International Journal of Cardiology, vol 344 (2021), page 149–159.
DOI:
https://doi.org/10.1016/j.ijcard.2021.09.046
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