SRX6714238 GSM4034926 SRP218341 SRS5267218 GSM4034926 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034926 GSM4034926 GEO Accession GSM4034926 SRX6714239 GSM4034927 SRP218341 SRS5267219 GSM4034927 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034927 GSM4034927 GEO Accession GSM4034927 SRX6714240 GSM4034928 SRP218341 SRS5267220 GSM4034928 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034928 GSM4034928 GEO Accession GSM4034928 SRX6714241 GSM4034929 SRP218341 SRS5267221 GSM4034929 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034929 GSM4034929 GEO Accession GSM4034929 SRX6714242 GSM4034930 SRP218341 SRS5267222 GSM4034930 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034930 GSM4034930 GEO Accession GSM4034930 SRX6714243 GSM4034931 SRP218341 SRS5267223 GSM4034931 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034931 GSM4034931 GEO Accession GSM4034931 SRX6714244 GSM4034932 SRP218341 SRS5267224 GSM4034932 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034932 GSM4034932 GEO Accession GSM4034932 SRX6714245 GSM4034933 SRP218341 SRS5267225 GSM4034933 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034933 GSM4034933 GEO Accession GSM4034933 SRX6714246 GSM4034934 SRP218341 SRS5267226 GSM4034934 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034934 GSM4034934 GEO Accession GSM4034934 SRX6714247 GSM4034935 SRP218341 SRS5267227 GSM4034935 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034935 GSM4034935 GEO Accession GSM4034935 SRX6714248 GSM4034936 SRP218341 SRS5267228 GSM4034936 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034936 GSM4034936 GEO Accession GSM4034936 SRX6714249 GSM4034937 SRP218341 SRS5267229 GSM4034937 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034937 GSM4034937 GEO Accession GSM4034937 SRX6714250 GSM4034938 SRP218341 SRS5267230 GSM4034938 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034938 GSM4034938 GEO Accession GSM4034938 SRX6714251 GSM4034939 SRP218341 SRS5267231 GSM4034939 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034939 GSM4034939 GEO Accession GSM4034939 SRX6714252 GSM4034940 SRP218341 SRS5267232 GSM4034940 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034940 GSM4034940 GEO Accession GSM4034940 SRX6714253 GSM4034941 SRP218341 SRS5267233 GSM4034941 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034941 GSM4034941 GEO Accession GSM4034941 SRX6714254 GSM4034942 SRP218341 SRS5267234 GSM4034942 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034942 GSM4034942 GEO Accession GSM4034942 SRX6714255 GSM4034943 SRP218341 SRS5267235 GSM4034943 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034943 GSM4034943 GEO Accession GSM4034943 SRX6714256 GSM4034944 SRP218341 SRS5267236 GSM4034944 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034944 GSM4034944 GEO Accession GSM4034944 SRX6714257 GSM4034945 SRP218341 SRS5267237 GSM4034945 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Direct-Zol RNA purification kit (Zymo Research) as recommended by manufacturer. 3'-endRNA libraries were prepared for sequencing using Lexogen QuantSeq 3' mRNA-Seq kit Illumina HiSeq 4000 gds 304034945 GSM4034945 GEO Accession GSM4034945 SRX6799402 GSM4059083 SRP218341 PRJNA560229 SRS5342406 GSM4059083 RNA-Seq TRANSCRIPTOMIC cDNA Cells from different genotypes/differentiations were harvested in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). In the case of cardiomyocytes, cells at D10-D11 of differentiation were used, while in the case of NCCs, cells were obtained by collecting migratory cells from dissected and re-plated rosettes. polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304059083 GSM4059083 GEO Accession GSM4059083 SRX6799403 GSM4059084 SRP218341 PRJNA560229 SRS5342407 GSM4059084 RNA-Seq TRANSCRIPTOMIC cDNA Cells from different genotypes/differentiations were harvested in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). In the case of cardiomyocytes, cells at D10-D11 of differentiation were used, while in the case of NCCs, cells were obtained by collecting migratory cells from dissected and re-plated rosettes. polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304059084 GSM4059084 GEO Accession GSM4059084 SRX6799404 GSM4059085 SRP218341 PRJNA560229 SRS5342408 GSM4059085 RNA-Seq TRANSCRIPTOMIC cDNA Cells from different genotypes/differentiations were harvested in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). In the case of cardiomyocytes, cells at D10-D11 of differentiation were used, while in the case of NCCs, cells were obtained by collecting migratory cells from dissected and re-plated rosettes. polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304059085 GSM4059085 GEO Accession GSM4059085 SRX6799405 GSM4059086 SRP218341 PRJNA560229 SRS5342409 GSM4059086 RNA-Seq TRANSCRIPTOMIC cDNA Cells from different genotypes/differentiations were harvested in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). In the case of cardiomyocytes, cells at D10-D11 of differentiation were used, while in the case of NCCs, cells were obtained by collecting migratory cells from dissected and re-plated rosettes. polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304059086 GSM4059086 GEO Accession GSM4059086 SRX6799406 GSM4059087 SRP218341 PRJNA560229 SRS5342410 GSM4059087 RNA-Seq TRANSCRIPTOMIC cDNA Cells from different genotypes/differentiations were harvested in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). In the case of cardiomyocytes, cells at D10-D11 of differentiation were used, while in the case of NCCs, cells were obtained by collecting migratory cells from dissected and re-plated rosettes. polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304059087 GSM4059087 GEO Accession GSM4059087 SRX6799407 GSM4059088 SRP218341 PRJNA560229 SRS5342411 GSM4059088 RNA-Seq TRANSCRIPTOMIC cDNA Cells from different genotypes/differentiations were harvested in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). In the case of cardiomyocytes, cells at D10-D11 of differentiation were used, while in the case of NCCs, cells were obtained by collecting migratory cells from dissected and re-plated rosettes. polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304059088 GSM4059088 GEO Accession GSM4059088 SRX6799408 GSM4059089 SRP218341 PRJNA560229 SRS5342412 GSM4059089 RNA-Seq TRANSCRIPTOMIC cDNA Cells from different genotypes/differentiations were harvested in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). In the case of cardiomyocytes, cells at D10-D11 of differentiation were used, while in the case of NCCs, cells were obtained by collecting migratory cells from dissected and re-plated rosettes. polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304059089 GSM4059089 GEO Accession GSM4059089 SRX6799409 GSM4059090 SRP218341 PRJNA560229 SRS5342413 GSM4059090 RNA-Seq TRANSCRIPTOMIC cDNA Cells from different genotypes/differentiations were harvested in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). In the case of cardiomyocytes, cells at D10-D11 of differentiation were used, while in the case of NCCs, cells were obtained by collecting migratory cells from dissected and re-plated rosettes. polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304059090 GSM4059090 GEO Accession GSM4059090 SRX6799410 GSM4059091 SRP218341 PRJNA560229 SRS5342414 GSM4059091 RNA-Seq TRANSCRIPTOMIC cDNA Cells from different genotypes/differentiations were harvested in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). In the case of cardiomyocytes, cells at D10-D11 of differentiation were used, while in the case of NCCs, cells were obtained by collecting migratory cells from dissected and re-plated rosettes. polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304059091 GSM4059091 GEO Accession GSM4059091 SRX6799411 GSM4059092 SRP218341 PRJNA560229 SRS5342415 GSM4059092 RNA-Seq TRANSCRIPTOMIC cDNA Cells from different genotypes/differentiations were harvested in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). In the case of cardiomyocytes, cells at D10-D11 of differentiation were used, while in the case of NCCs, cells were obtained by collecting migratory cells from dissected and re-plated rosettes. polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304059092 GSM4059092 GEO Accession GSM4059092 SRX6799412 GSM4059093 SRP218341 PRJNA560229 SRS5342416 GSM4059093 RNA-Seq TRANSCRIPTOMIC cDNA Cells from different genotypes/differentiations were harvested in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). In the case of cardiomyocytes, cells at D10-D11 of differentiation were used, while in the case of NCCs, cells were obtained by collecting migratory cells from dissected and re-plated rosettes. polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304059093 GSM4059093 GEO Accession GSM4059093 SRX6799413 GSM4059094 SRP218341 PRJNA560229 SRS5342417 GSM4059094 RNA-Seq TRANSCRIPTOMIC cDNA Cells from different genotypes/differentiations were harvested in Trizol (Life Technologies) and total RNA was isolated and DNase-treated using the Direct-zol RNA miniprep kit as per manufacturer's instructions (Zymo Research). In the case of cardiomyocytes, cells at D10-D11 of differentiation were used, while in the case of NCCs, cells were obtained by collecting migratory cells from dissected and re-plated rosettes. polyA-enriched RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304059094 GSM4059094 GEO Accession GSM4059094