SRX3781640 GSM3036928 SRP134911 SRS3035065 GSM3036928 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA of oocytes were purified using RNeasy Mini kit (QIAGEN, 74104) as recommended protocols First stand cDNA was synthesized using a commercial kit (Invitrogen, Cat. 18080-051). Second strand cDNA was synthesized with second strand synthesis buffer (Invitrogen, Cat. 10812014), MgCl2, DTT, dNTP, dUTP, RNase H (Fermentas, Cat. EN0202), E. coli DNA ligase (NEB, Cat. M0205S) and DNA polymerase I (NEB, Cat. M0209S). DNA was purified after 2-hour incubation on thermomixer at 16°C. Synthesized cDNA was subjected to library preparation. DNA was end-repaired, adenylated, and ligated to TruSeq sequencing adaptors. Libraries were then treated with UDG (AMPErase, Cat. N808-0096) at 37°C for 1 hour followed by DNA amplification using Phusion HF DNA polymerase (NEB, Cat. M0530L). The amplified DNA was size selected using AMPure Beads for 200-500bp DNA fragments. HiSeq X Ten gds 303036928 GSM3036928 GEO Accession GSM3036928 SRX3781641 GSM3036929 SRP134911 SRS3035066 GSM3036929 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA of oocytes were purified using RNeasy Mini kit (QIAGEN, 74104) as recommended protocols First stand cDNA was synthesized using a commercial kit (Invitrogen, Cat. 18080-051). Second strand cDNA was synthesized with second strand synthesis buffer (Invitrogen, Cat. 10812014), MgCl2, DTT, dNTP, dUTP, RNase H (Fermentas, Cat. EN0202), E. coli DNA ligase (NEB, Cat. M0205S) and DNA polymerase I (NEB, Cat. M0209S). DNA was purified after 2-hour incubation on thermomixer at 16°C. Synthesized cDNA was subjected to library preparation. DNA was end-repaired, adenylated, and ligated to TruSeq sequencing adaptors. Libraries were then treated with UDG (AMPErase, Cat. N808-0096) at 37°C for 1 hour followed by DNA amplification using Phusion HF DNA polymerase (NEB, Cat. M0530L). The amplified DNA was size selected using AMPure Beads for 200-500bp DNA fragments. HiSeq X Ten gds 303036929 GSM3036929 GEO Accession GSM3036929 SRX3781642 GSM3036930 SRP134911 SRS3035067 GSM3036930 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA of oocytes were purified using RNeasy Mini kit (QIAGEN, 74104) as recommended protocols First stand cDNA was synthesized using a commercial kit (Invitrogen, Cat. 18080-051). Second strand cDNA was synthesized with second strand synthesis buffer (Invitrogen, Cat. 10812014), MgCl2, DTT, dNTP, dUTP, RNase H (Fermentas, Cat. EN0202), E. coli DNA ligase (NEB, Cat. M0205S) and DNA polymerase I (NEB, Cat. M0209S). DNA was purified after 2-hour incubation on thermomixer at 16°C. Synthesized cDNA was subjected to library preparation. DNA was end-repaired, adenylated, and ligated to TruSeq sequencing adaptors. Libraries were then treated with UDG (AMPErase, Cat. N808-0096) at 37°C for 1 hour followed by DNA amplification using Phusion HF DNA polymerase (NEB, Cat. M0530L). The amplified DNA was size selected using AMPure Beads for 200-500bp DNA fragments. HiSeq X Ten gds 303036930 GSM3036930 GEO Accession GSM3036930 SRX3781643 GSM3036931 SRP134911 SRS3035068 GSM3036931 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA of oocytes were purified using RNeasy Mini kit (QIAGEN, 74104) as recommended protocols First stand cDNA was synthesized using a commercial kit (Invitrogen, Cat. 18080-051). Second strand cDNA was synthesized with second strand synthesis buffer (Invitrogen, Cat. 10812014), MgCl2, DTT, dNTP, dUTP, RNase H (Fermentas, Cat. EN0202), E. coli DNA ligase (NEB, Cat. M0205S) and DNA polymerase I (NEB, Cat. M0209S). DNA was purified after 2-hour incubation on thermomixer at 16°C. Synthesized cDNA was subjected to library preparation. DNA was end-repaired, adenylated, and ligated to TruSeq sequencing adaptors. Libraries were then treated with UDG (AMPErase, Cat. N808-0096) at 37°C for 1 hour followed by DNA amplification using Phusion HF DNA polymerase (NEB, Cat. M0530L). The amplified DNA was size selected using AMPure Beads for 200-500bp DNA fragments. HiSeq X Ten gds 303036931 GSM3036931 GEO Accession GSM3036931 SRX3781644 GSM3036932 SRP134911 SRS3035069 GSM3036932 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA of oocytes were purified using RNeasy Mini kit (QIAGEN, 74104) as recommended protocols First stand cDNA was synthesized using a commercial kit (Invitrogen, Cat. 18080-051). Second strand cDNA was synthesized with second strand synthesis buffer (Invitrogen, Cat. 10812014), MgCl2, DTT, dNTP, dUTP, RNase H (Fermentas, Cat. EN0202), E. coli DNA ligase (NEB, Cat. M0205S) and DNA polymerase I (NEB, Cat. M0209S). DNA was purified after 2-hour incubation on thermomixer at 16°C. Synthesized cDNA was subjected to library preparation. DNA was end-repaired, adenylated, and ligated to TruSeq sequencing adaptors. Libraries were then treated with UDG (AMPErase, Cat. N808-0096) at 37°C for 1 hour followed by DNA amplification using Phusion HF DNA polymerase (NEB, Cat. M0530L). The amplified DNA was size selected using AMPure Beads for 200-500bp DNA fragments. HiSeq X Ten gds 303036932 GSM3036932 GEO Accession GSM3036932 SRX3781645 GSM3036933 SRP134911 SRS3035070 GSM3036933 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA of oocytes were purified using RNeasy Mini kit (QIAGEN, 74104) as recommended protocols First stand cDNA was synthesized using a commercial kit (Invitrogen, Cat. 18080-051). Second strand cDNA was synthesized with second strand synthesis buffer (Invitrogen, Cat. 10812014), MgCl2, DTT, dNTP, dUTP, RNase H (Fermentas, Cat. EN0202), E. coli DNA ligase (NEB, Cat. M0205S) and DNA polymerase I (NEB, Cat. M0209S). DNA was purified after 2-hour incubation on thermomixer at 16°C. Synthesized cDNA was subjected to library preparation. DNA was end-repaired, adenylated, and ligated to TruSeq sequencing adaptors. Libraries were then treated with UDG (AMPErase, Cat. N808-0096) at 37°C for 1 hour followed by DNA amplification using Phusion HF DNA polymerase (NEB, Cat. M0530L). The amplified DNA was size selected using AMPure Beads for 200-500bp DNA fragments. HiSeq X Ten gds 303036933 GSM3036933 GEO Accession GSM3036933 SRX3781646 GSM3036934 SRP134911 SRS3035071 GSM3036934 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA of oocytes were purified using RNeasy Mini kit (QIAGEN, 74104) as recommended protocols First stand cDNA was synthesized using a commercial kit (Invitrogen, Cat. 18080-051). Second strand cDNA was synthesized with second strand synthesis buffer (Invitrogen, Cat. 10812014), MgCl2, DTT, dNTP, dUTP, RNase H (Fermentas, Cat. EN0202), E. coli DNA ligase (NEB, Cat. M0205S) and DNA polymerase I (NEB, Cat. M0209S). DNA was purified after 2-hour incubation on thermomixer at 16°C. Synthesized cDNA was subjected to library preparation. DNA was end-repaired, adenylated, and ligated to TruSeq sequencing adaptors. Libraries were then treated with UDG (AMPErase, Cat. N808-0096) at 37°C for 1 hour followed by DNA amplification using Phusion HF DNA polymerase (NEB, Cat. M0530L). The amplified DNA was size selected using AMPure Beads for 200-500bp DNA fragments. HiSeq X Ten gds 303036934 GSM3036934 GEO Accession GSM3036934 SRX3781647 GSM3036935 SRP134911 SRS3035072 GSM3036935 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA of oocytes were purified using RNeasy Mini kit (QIAGEN, 74104) as recommended protocols First stand cDNA was synthesized using a commercial kit (Invitrogen, Cat. 18080-051). Second strand cDNA was synthesized with second strand synthesis buffer (Invitrogen, Cat. 10812014), MgCl2, DTT, dNTP, dUTP, RNase H (Fermentas, Cat. EN0202), E. coli DNA ligase (NEB, Cat. M0205S) and DNA polymerase I (NEB, Cat. M0209S). DNA was purified after 2-hour incubation on thermomixer at 16°C. Synthesized cDNA was subjected to library preparation. DNA was end-repaired, adenylated, and ligated to TruSeq sequencing adaptors. Libraries were then treated with UDG (AMPErase, Cat. N808-0096) at 37°C for 1 hour followed by DNA amplification using Phusion HF DNA polymerase (NEB, Cat. M0530L). The amplified DNA was size selected using AMPure Beads for 200-500bp DNA fragments. HiSeq X Ten gds 303036935 GSM3036935 GEO Accession GSM3036935 SRX3781648 GSM3036936 SRP134911 SRS3035073 GSM3036936 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA of oocytes were purified using RNeasy Mini kit (QIAGEN, 74104) as recommended protocols First stand cDNA was synthesized using a commercial kit (Invitrogen, Cat. 18080-051). Second strand cDNA was synthesized with second strand synthesis buffer (Invitrogen, Cat. 10812014), MgCl2, DTT, dNTP, dUTP, RNase H (Fermentas, Cat. EN0202), E. coli DNA ligase (NEB, Cat. M0205S) and DNA polymerase I (NEB, Cat. M0209S). DNA was purified after 2-hour incubation on thermomixer at 16°C. Synthesized cDNA was subjected to library preparation. DNA was end-repaired, adenylated, and ligated to TruSeq sequencing adaptors. Libraries were then treated with UDG (AMPErase, Cat. N808-0096) at 37°C for 1 hour followed by DNA amplification using Phusion HF DNA polymerase (NEB, Cat. M0530L). The amplified DNA was size selected using AMPure Beads for 200-500bp DNA fragments. HiSeq X Ten gds 303036936 GSM3036936 GEO Accession GSM3036936