SRX645365 GSM1426195 SRP044043 SRS653531 GSM1426195 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were directly lysed and used for cDNA synthesis using SMARTer Ultra Low Input RNA cDNA preparation kit (Clontech). After amplification, the cDNA samples were fragmented using Covaris sonicator (Covaris). Sequencing libraries were made with the fragmented DNA using NEBNext Ultra DNA Library Prep Kit for Illumina according to manufacturer’s instruction (New England Biolabs). Single end 50 bp sequencing was done on Hiseq 2500 (Illumina). Illumina HiSeq 2500 GEO Sample GSM1426195 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1426195 gds 301426195 GEO Accession GSM1426195 SRX645366 GSM1426196 SRP044043 SRS653532 GSM1426196 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were directly lysed and used for cDNA synthesis using SMARTer Ultra Low Input RNA cDNA preparation kit (Clontech). After amplification, the cDNA samples were fragmented using Covaris sonicator (Covaris). Sequencing libraries were made with the fragmented DNA using NEBNext Ultra DNA Library Prep Kit for Illumina according to manufacturer’s instruction (New England Biolabs). Single end 50 bp sequencing was done on Hiseq 2500 (Illumina). Illumina HiSeq 2500 GEO Sample GSM1426196 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1426196 gds 301426196 GEO Accession GSM1426196 SRX645367 GSM1426197 SRP044043 SRS653533 GSM1426197 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were directly lysed and used for cDNA synthesis using SMARTer Ultra Low Input RNA cDNA preparation kit (Clontech). After amplification, the cDNA samples were fragmented using Covaris sonicator (Covaris). Sequencing libraries were made with the fragmented DNA using NEBNext Ultra DNA Library Prep Kit for Illumina according to manufacturer’s instruction (New England Biolabs). Single end 50 bp sequencing was done on Hiseq 2500 (Illumina). Illumina HiSeq 2500 GEO Sample GSM1426197 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1426197 gds 301426197 GEO Accession GSM1426197 SRX645368 GSM1426198 SRP044043 SRS653534 GSM1426198 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were directly lysed and used for cDNA synthesis using SMARTer Ultra Low Input RNA cDNA preparation kit (Clontech). After amplification, the cDNA samples were fragmented using Covaris sonicator (Covaris). Sequencing libraries were made with the fragmented DNA using NEBNext Ultra DNA Library Prep Kit for Illumina according to manufacturer’s instruction (New England Biolabs). Single end 50 bp sequencing was done on Hiseq 2500 (Illumina). Illumina HiSeq 2500 GEO Sample GSM1426198 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1426198 gds 301426198 GEO Accession GSM1426198 SRX645369 GSM1426199 SRP044043 SRS653535 GSM1426199 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were directly lysed and used for cDNA synthesis using SMARTer Ultra Low Input RNA cDNA preparation kit (Clontech). After amplification, the cDNA samples were fragmented using Covaris sonicator (Covaris). Sequencing libraries were made with the fragmented DNA using NEBNext Ultra DNA Library Prep Kit for Illumina according to manufacturer’s instruction (New England Biolabs). Single end 50 bp sequencing was done on Hiseq 2500 (Illumina). Illumina HiSeq 2500 GEO Sample GSM1426199 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1426199 gds 301426199 GEO Accession GSM1426199 SRX645370 GSM1426200 SRP044043 SRS653536 GSM1426200 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were directly lysed and used for cDNA synthesis using SMARTer Ultra Low Input RNA cDNA preparation kit (Clontech). After amplification, the cDNA samples were fragmented using Covaris sonicator (Covaris). Sequencing libraries were made with the fragmented DNA using NEBNext Ultra DNA Library Prep Kit for Illumina according to manufacturer’s instruction (New England Biolabs). Single end 50 bp sequencing was done on Hiseq 2500 (Illumina). Illumina HiSeq 2500 GEO Sample GSM1426200 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1426200 gds 301426200 GEO Accession GSM1426200 SRX645371 GSM1426201 SRP044043 SRS653537 GSM1426201 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were directly lysed and used for cDNA synthesis using SMARTer Ultra Low Input RNA cDNA preparation kit (Clontech). After amplification, the cDNA samples were fragmented using Covaris sonicator (Covaris). Sequencing libraries were made with the fragmented DNA using NEBNext Ultra DNA Library Prep Kit for Illumina according to manufacturer’s instruction (New England Biolabs). Single end 50 bp sequencing was done on Hiseq 2500 (Illumina). Illumina HiSeq 2500 GEO Sample GSM1426201 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1426201 gds 301426201 GEO Accession GSM1426201 SRX645372 GSM1426202 SRP044043 SRS653538 GSM1426202 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were directly lysed and used for cDNA synthesis using SMARTer Ultra Low Input RNA cDNA preparation kit (Clontech). After amplification, the cDNA samples were fragmented using Covaris sonicator (Covaris). Sequencing libraries were made with the fragmented DNA using NEBNext Ultra DNA Library Prep Kit for Illumina according to manufacturer’s instruction (New England Biolabs). Single end 50 bp sequencing was done on Hiseq 2500 (Illumina). Illumina HiSeq 2500 GEO Sample GSM1426202 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1426202 gds 301426202 GEO Accession GSM1426202 SRX645373 GSM1426203 SRP044043 SRS653539 GSM1426203 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were directly lysed and used for cDNA synthesis using SMARTer Ultra Low Input RNA cDNA preparation kit (Clontech). After amplification, the cDNA samples were fragmented using Covaris sonicator (Covaris). Sequencing libraries were made with the fragmented DNA using NEBNext Ultra DNA Library Prep Kit for Illumina according to manufacturer’s instruction (New England Biolabs). Single end 50 bp sequencing was done on Hiseq 2500 (Illumina). Illumina HiSeq 2500 GEO Sample GSM1426203 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1426203 gds 301426203 GEO Accession GSM1426203 SRX645374 GSM1426204 SRP044043 SRS653540 GSM1426204 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were directly lysed and used for cDNA synthesis using SMARTer Ultra Low Input RNA cDNA preparation kit (Clontech). After amplification, the cDNA samples were fragmented using Covaris sonicator (Covaris). Sequencing libraries were made with the fragmented DNA using NEBNext Ultra DNA Library Prep Kit for Illumina according to manufacturer’s instruction (New England Biolabs). Single end 50 bp sequencing was done on Hiseq 2500 (Illumina). Illumina HiSeq 2500 GEO Sample GSM1426204 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1426204 gds 301426204 GEO Accession GSM1426204 SRX645375 GSM1426205 SRP044043 SRS653541 GSM1426205 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were directly lysed and used for cDNA synthesis using SMARTer Ultra Low Input RNA cDNA preparation kit (Clontech). After amplification, the cDNA samples were fragmented using Covaris sonicator (Covaris). Sequencing libraries were made with the fragmented DNA using NEBNext Ultra DNA Library Prep Kit for Illumina according to manufacturer’s instruction (New England Biolabs). Single end 50 bp sequencing was done on Hiseq 2500 (Illumina). Illumina HiSeq 2500 GEO Sample GSM1426205 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1426205 gds 301426205 GEO Accession GSM1426205 SRX645376 GSM1426206 SRP044043 SRS653542 GSM1426206 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were directly lysed and used for cDNA synthesis using SMARTer Ultra Low Input RNA cDNA preparation kit (Clontech). After amplification, the cDNA samples were fragmented using Covaris sonicator (Covaris). Sequencing libraries were made with the fragmented DNA using NEBNext Ultra DNA Library Prep Kit for Illumina according to manufacturer’s instruction (New England Biolabs). Single end 50 bp sequencing was done on Hiseq 2500 (Illumina). Illumina HiSeq 2500 GEO Sample GSM1426206 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1426206 gds 301426206 GEO Accession GSM1426206 SRX645377 GSM1426207 SRP044043 SRS653543 GSM1426207 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were directly lysed and used for cDNA synthesis using SMARTer Ultra Low Input RNA cDNA preparation kit (Clontech). After amplification, the cDNA samples were fragmented using Covaris sonicator (Covaris). Sequencing libraries were made with the fragmented DNA using NEBNext Ultra DNA Library Prep Kit for Illumina according to manufacturer’s instruction (New England Biolabs). Single end 50 bp sequencing was done on Hiseq 2500 (Illumina). Illumina HiSeq 2500 GEO Sample GSM1426207 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1426207 gds 301426207 GEO Accession GSM1426207 SRX645378 GSM1426208 SRP044043 SRS653544 GSM1426208 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were directly lysed and used for cDNA synthesis using SMARTer Ultra Low Input RNA cDNA preparation kit (Clontech). After amplification, the cDNA samples were fragmented using Covaris sonicator (Covaris). Sequencing libraries were made with the fragmented DNA using NEBNext Ultra DNA Library Prep Kit for Illumina according to manufacturer’s instruction (New England Biolabs). Single end 50 bp sequencing was done on Hiseq 2500 (Illumina). Illumina HiSeq 2500 GEO Sample GSM1426208 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1426208 gds 301426208 GEO Accession GSM1426208