SRX2209219 GSM2334957 SRP090801 SRS1726580 GSM2334957 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Arcturus Pico Pure (Thermofisher) following manufacturer instructions. 0.6 ng of total RNA was used to generate barcoded RNA-seq libraries using the Ovation Single Cell RNA-Seq System (NuGEN) with two rounds of library amplification. The size of the libraries was calculated using the Agilent 2100 Bioanalyzer. Library concentration was determined using the Qubit® fluorometer (ThermoFisher Scientific). Libraries were sequenced on a HiSeq2500 (Illumina) to generate 60 bases single reads. 4 biological replicates consisting of 5 pooled hearts were used per sample. Illumina HiSeq 2500 gds 302334957 GEO Accession GSM2334957 SRX2209220 GSM2334958 SRP090801 SRS1726582 GSM2334958 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Arcturus Pico Pure (Thermofisher) following manufacturer instructions. 0.6 ng of total RNA was used to generate barcoded RNA-seq libraries using the Ovation Single Cell RNA-Seq System (NuGEN) with two rounds of library amplification. The size of the libraries was calculated using the Agilent 2100 Bioanalyzer. Library concentration was determined using the Qubit® fluorometer (ThermoFisher Scientific). Libraries were sequenced on a HiSeq2500 (Illumina) to generate 60 bases single reads. 4 biological replicates consisting of 5 pooled hearts were used per sample. Illumina HiSeq 2500 gds 302334958 GEO Accession GSM2334958 SRX2209221 GSM2334959 SRP090801 SRS1726581 GSM2334959 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Arcturus Pico Pure (Thermofisher) following manufacturer instructions. 0.6 ng of total RNA was used to generate barcoded RNA-seq libraries using the Ovation Single Cell RNA-Seq System (NuGEN) with two rounds of library amplification. The size of the libraries was calculated using the Agilent 2100 Bioanalyzer. Library concentration was determined using the Qubit® fluorometer (ThermoFisher Scientific). Libraries were sequenced on a HiSeq2500 (Illumina) to generate 60 bases single reads. 4 biological replicates consisting of 5 pooled hearts were used per sample. Illumina HiSeq 2500 gds 302334959 GEO Accession GSM2334959 SRX2209222 GSM2334960 SRP090801 SRS1726583 GSM2334960 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Arcturus Pico Pure (Thermofisher) following manufacturer instructions. 0.6 ng of total RNA was used to generate barcoded RNA-seq libraries using the Ovation Single Cell RNA-Seq System (NuGEN) with two rounds of library amplification. The size of the libraries was calculated using the Agilent 2100 Bioanalyzer. Library concentration was determined using the Qubit® fluorometer (ThermoFisher Scientific). Libraries were sequenced on a HiSeq2500 (Illumina) to generate 60 bases single reads. 4 biological replicates consisting of 5 pooled hearts were used per sample. Illumina HiSeq 2500 gds 302334960 GEO Accession GSM2334960 SRX2209223 GSM2334961 SRP090801 SRS1726584 GSM2334961 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Arcturus Pico Pure (Thermofisher) following manufacturer instructions. 0.6 ng of total RNA was used to generate barcoded RNA-seq libraries using the Ovation Single Cell RNA-Seq System (NuGEN) with two rounds of library amplification. The size of the libraries was calculated using the Agilent 2100 Bioanalyzer. Library concentration was determined using the Qubit® fluorometer (ThermoFisher Scientific). Libraries were sequenced on a HiSeq2500 (Illumina) to generate 60 bases single reads. 4 biological replicates consisting of 5 pooled hearts were used per sample. Illumina HiSeq 2500 gds 302334961 GEO Accession GSM2334961 SRX2209224 GSM2334962 SRP090801 SRS1726585 GSM2334962 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Arcturus Pico Pure (Thermofisher) following manufacturer instructions. 0.6 ng of total RNA was used to generate barcoded RNA-seq libraries using the Ovation Single Cell RNA-Seq System (NuGEN) with two rounds of library amplification. The size of the libraries was calculated using the Agilent 2100 Bioanalyzer. Library concentration was determined using the Qubit® fluorometer (ThermoFisher Scientific). Libraries were sequenced on a HiSeq2500 (Illumina) to generate 60 bases single reads. 4 biological replicates consisting of 5 pooled hearts were used per sample. Illumina HiSeq 2500 gds 302334962 GEO Accession GSM2334962 SRX2209225 GSM2334963 SRP090801 SRS1726587 GSM2334963 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Arcturus Pico Pure (Thermofisher) following manufacturer instructions. 0.6 ng of total RNA was used to generate barcoded RNA-seq libraries using the Ovation Single Cell RNA-Seq System (NuGEN) with two rounds of library amplification. The size of the libraries was calculated using the Agilent 2100 Bioanalyzer. Library concentration was determined using the Qubit® fluorometer (ThermoFisher Scientific). Libraries were sequenced on a HiSeq2500 (Illumina) to generate 60 bases single reads. 4 biological replicates consisting of 5 pooled hearts were used per sample. Illumina HiSeq 2500 gds 302334963 GEO Accession GSM2334963 SRX2209226 GSM2334964 SRP090801 SRS1726586 GSM2334964 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Arcturus Pico Pure (Thermofisher) following manufacturer instructions. 0.6 ng of total RNA was used to generate barcoded RNA-seq libraries using the Ovation Single Cell RNA-Seq System (NuGEN) with two rounds of library amplification. The size of the libraries was calculated using the Agilent 2100 Bioanalyzer. Library concentration was determined using the Qubit® fluorometer (ThermoFisher Scientific). Libraries were sequenced on a HiSeq2500 (Illumina) to generate 60 bases single reads. 4 biological replicates consisting of 5 pooled hearts were used per sample. Illumina HiSeq 2500 gds 302334964 GEO Accession GSM2334964