SRX7184552 GSM4178123 SRP230630 SRS5690776 GSM4178123 RNA-Seq TRANSCRIPTOMIC cDNA Myocardium were removed, flash frozen on dry ice, and total RNA was isolated from tissue and cell specimens using Trizol reagent (Invitrogen).1-2 µg total RNA was used to prepare the sequencing library. (1) Total RNA is enriched by oligo (dT) magnetic beads (rRNA removed); (2) RNA-seq library preparation using KAPA Stranded RNA-Seq Library Prep Kit (Illumina), which incorporates dUTP into the second cDNA strand and renders the RNA-seq library strand-specific. The completed libraries were qualified with Agilent 2100 Bioanalyzer and quantified by the absolute quantification qPCR method. To sequence the libraries on the Illumina HiSeq 4000 instrument, the barcoded libraries were mixed, denatured to single-stranded DNA in NaOH, captured on Illumina flow cell, amplified in situ, and subsequently sequenced for 150 cycles for both ends on Illumina HiSeq instrument. Illumina HiSeq 4000 gds 304178123 GSM4178123 GEO Accession GSM4178123 SRX7184553 GSM4178124 SRP230630 SRS5690777 GSM4178124 RNA-Seq TRANSCRIPTOMIC cDNA Myocardium were removed, flash frozen on dry ice, and total RNA was isolated from tissue and cell specimens using Trizol reagent (Invitrogen).1-2 µg total RNA was used to prepare the sequencing library. (1) Total RNA is enriched by oligo (dT) magnetic beads (rRNA removed); (2) RNA-seq library preparation using KAPA Stranded RNA-Seq Library Prep Kit (Illumina), which incorporates dUTP into the second cDNA strand and renders the RNA-seq library strand-specific. The completed libraries were qualified with Agilent 2100 Bioanalyzer and quantified by the absolute quantification qPCR method. To sequence the libraries on the Illumina HiSeq 4000 instrument, the barcoded libraries were mixed, denatured to single-stranded DNA in NaOH, captured on Illumina flow cell, amplified in situ, and subsequently sequenced for 150 cycles for both ends on Illumina HiSeq instrument. Illumina HiSeq 4000 gds 304178124 GSM4178124 GEO Accession GSM4178124 SRX7184554 GSM4178125 SRP230630 SRS5690778 GSM4178125 RNA-Seq TRANSCRIPTOMIC cDNA Myocardium were removed, flash frozen on dry ice, and total RNA was isolated from tissue and cell specimens using Trizol reagent (Invitrogen).1-2 µg total RNA was used to prepare the sequencing library. (1) Total RNA is enriched by oligo (dT) magnetic beads (rRNA removed); (2) RNA-seq library preparation using KAPA Stranded RNA-Seq Library Prep Kit (Illumina), which incorporates dUTP into the second cDNA strand and renders the RNA-seq library strand-specific. The completed libraries were qualified with Agilent 2100 Bioanalyzer and quantified by the absolute quantification qPCR method. To sequence the libraries on the Illumina HiSeq 4000 instrument, the barcoded libraries were mixed, denatured to single-stranded DNA in NaOH, captured on Illumina flow cell, amplified in situ, and subsequently sequenced for 150 cycles for both ends on Illumina HiSeq instrument. Illumina HiSeq 4000 gds 304178125 GSM4178125 GEO Accession GSM4178125 SRX7184555 GSM4178126 SRP230630 SRS5690779 GSM4178126 RNA-Seq TRANSCRIPTOMIC cDNA Myocardium were removed, flash frozen on dry ice, and total RNA was isolated from tissue and cell specimens using Trizol reagent (Invitrogen).1-2 µg total RNA was used to prepare the sequencing library. (1) Total RNA is enriched by oligo (dT) magnetic beads (rRNA removed); (2) RNA-seq library preparation using KAPA Stranded RNA-Seq Library Prep Kit (Illumina), which incorporates dUTP into the second cDNA strand and renders the RNA-seq library strand-specific. The completed libraries were qualified with Agilent 2100 Bioanalyzer and quantified by the absolute quantification qPCR method. To sequence the libraries on the Illumina HiSeq 4000 instrument, the barcoded libraries were mixed, denatured to single-stranded DNA in NaOH, captured on Illumina flow cell, amplified in situ, and subsequently sequenced for 150 cycles for both ends on Illumina HiSeq instrument. Illumina HiSeq 4000 gds 304178126 GSM4178126 GEO Accession GSM4178126 SRX7184556 GSM4178127 SRP230630 SRS5690780 GSM4178127 RNA-Seq TRANSCRIPTOMIC cDNA Myocardium were removed, flash frozen on dry ice, and total RNA was isolated from tissue and cell specimens using Trizol reagent (Invitrogen).1-2 µg total RNA was used to prepare the sequencing library. (1) Total RNA is enriched by oligo (dT) magnetic beads (rRNA removed); (2) RNA-seq library preparation using KAPA Stranded RNA-Seq Library Prep Kit (Illumina), which incorporates dUTP into the second cDNA strand and renders the RNA-seq library strand-specific. The completed libraries were qualified with Agilent 2100 Bioanalyzer and quantified by the absolute quantification qPCR method. To sequence the libraries on the Illumina HiSeq 4000 instrument, the barcoded libraries were mixed, denatured to single-stranded DNA in NaOH, captured on Illumina flow cell, amplified in situ, and subsequently sequenced for 150 cycles for both ends on Illumina HiSeq instrument. Illumina HiSeq 4000 gds 304178127 GSM4178127 GEO Accession GSM4178127 SRX7184557 GSM4178128 SRP230630 SRS5690781 GSM4178128 RNA-Seq TRANSCRIPTOMIC cDNA Myocardium were removed, flash frozen on dry ice, and total RNA was isolated from tissue and cell specimens using Trizol reagent (Invitrogen).1-2 µg total RNA was used to prepare the sequencing library. (1) Total RNA is enriched by oligo (dT) magnetic beads (rRNA removed); (2) RNA-seq library preparation using KAPA Stranded RNA-Seq Library Prep Kit (Illumina), which incorporates dUTP into the second cDNA strand and renders the RNA-seq library strand-specific. The completed libraries were qualified with Agilent 2100 Bioanalyzer and quantified by the absolute quantification qPCR method. To sequence the libraries on the Illumina HiSeq 4000 instrument, the barcoded libraries were mixed, denatured to single-stranded DNA in NaOH, captured on Illumina flow cell, amplified in situ, and subsequently sequenced for 150 cycles for both ends on Illumina HiSeq instrument. Illumina HiSeq 4000 gds 304178128 GSM4178128 GEO Accession GSM4178128 SRX7184558 GSM4178129 SRP230630 SRS5690782 GSM4178129 RNA-Seq TRANSCRIPTOMIC cDNA Myocardium were removed, flash frozen on dry ice, and total RNA was isolated from tissue and cell specimens using Trizol reagent (Invitrogen).1-2 µg total RNA was used to prepare the sequencing library. (1) Total RNA is enriched by oligo (dT) magnetic beads (rRNA removed); (2) RNA-seq library preparation using KAPA Stranded RNA-Seq Library Prep Kit (Illumina), which incorporates dUTP into the second cDNA strand and renders the RNA-seq library strand-specific. The completed libraries were qualified with Agilent 2100 Bioanalyzer and quantified by the absolute quantification qPCR method. To sequence the libraries on the Illumina HiSeq 4000 instrument, the barcoded libraries were mixed, denatured to single-stranded DNA in NaOH, captured on Illumina flow cell, amplified in situ, and subsequently sequenced for 150 cycles for both ends on Illumina HiSeq instrument. Illumina HiSeq 4000 gds 304178129 GSM4178129 GEO Accession GSM4178129 SRX7184559 GSM4178130 SRP230630 SRS5690783 GSM4178130 RNA-Seq TRANSCRIPTOMIC cDNA Myocardium were removed, flash frozen on dry ice, and total RNA was isolated from tissue and cell specimens using Trizol reagent (Invitrogen).1-2 µg total RNA was used to prepare the sequencing library. (1) Total RNA is enriched by oligo (dT) magnetic beads (rRNA removed); (2) RNA-seq library preparation using KAPA Stranded RNA-Seq Library Prep Kit (Illumina), which incorporates dUTP into the second cDNA strand and renders the RNA-seq library strand-specific. The completed libraries were qualified with Agilent 2100 Bioanalyzer and quantified by the absolute quantification qPCR method. To sequence the libraries on the Illumina HiSeq 4000 instrument, the barcoded libraries were mixed, denatured to single-stranded DNA in NaOH, captured on Illumina flow cell, amplified in situ, and subsequently sequenced for 150 cycles for both ends on Illumina HiSeq instrument. Illumina HiSeq 4000 gds 304178130 GSM4178130 GEO Accession GSM4178130 SRX7184560 GSM4178131 SRP230630 SRS5690784 GSM4178131 RNA-Seq TRANSCRIPTOMIC cDNA Myocardium were removed, flash frozen on dry ice, and total RNA was isolated from tissue and cell specimens using Trizol reagent (Invitrogen).1-2 µg total RNA was used to prepare the sequencing library. (1) Total RNA is enriched by oligo (dT) magnetic beads (rRNA removed); (2) RNA-seq library preparation using KAPA Stranded RNA-Seq Library Prep Kit (Illumina), which incorporates dUTP into the second cDNA strand and renders the RNA-seq library strand-specific. The completed libraries were qualified with Agilent 2100 Bioanalyzer and quantified by the absolute quantification qPCR method. To sequence the libraries on the Illumina HiSeq 4000 instrument, the barcoded libraries were mixed, denatured to single-stranded DNA in NaOH, captured on Illumina flow cell, amplified in situ, and subsequently sequenced for 150 cycles for both ends on Illumina HiSeq instrument. Illumina HiSeq 4000 gds 304178131 GSM4178131 GEO Accession GSM4178131 SRX7184561 GSM4178132 SRP230630 SRS5690785 GSM4178132 RNA-Seq TRANSCRIPTOMIC cDNA Myocardium were removed, flash frozen on dry ice, and total RNA was isolated from tissue and cell specimens using Trizol reagent (Invitrogen).1-2 µg total RNA was used to prepare the sequencing library. (1) Total RNA is enriched by oligo (dT) magnetic beads (rRNA removed); (2) RNA-seq library preparation using KAPA Stranded RNA-Seq Library Prep Kit (Illumina), which incorporates dUTP into the second cDNA strand and renders the RNA-seq library strand-specific. The completed libraries were qualified with Agilent 2100 Bioanalyzer and quantified by the absolute quantification qPCR method. To sequence the libraries on the Illumina HiSeq 4000 instrument, the barcoded libraries were mixed, denatured to single-stranded DNA in NaOH, captured on Illumina flow cell, amplified in situ, and subsequently sequenced for 150 cycles for both ends on Illumina HiSeq instrument. Illumina HiSeq 4000 gds 304178132 GSM4178132 GEO Accession GSM4178132