GSM2877811: Primordial_follicle_A10O; Homo sapiens; RNA-Seq

SRX3447165 GSM2877811 GSM2877811: Primordial_follicle_A10O; Homo sapiens; RNA-Seq SRP126216 SRS2737117 GSM2877811 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877811 GSM2877811 GEO Accession GSM2877811 SRX3447166 GSM2877812 GSM2877812: Primordial_follicle_A16O; Homo sapiens; RNA-Seq SRP126216 SRS2737119 GSM2877812 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877812 GSM2877812 GEO Accession GSM2877812 SRX3447167 GSM2877813 GSM2877813: Primordial_follicle_A6O; Homo sapiens; RNA-Seq SRP126216 SRS2737118 GSM2877813 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877813 GSM2877813 GEO Accession GSM2877813 SRX3447168 GSM2877814 GSM2877814: Primordial_follicle_A8O; Homo sapiens; RNA-Seq SRP126216 SRS2737120 GSM2877814 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877814 GSM2877814 GEO Accession GSM2877814 SRX3447169 GSM2877815 GSM2877815: Primordial_follicle_A9O; Homo sapiens; RNA-Seq SRP126216 SRS2737121 GSM2877815 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877815 GSM2877815 GEO Accession GSM2877815 SRX3447170 GSM2877816 GSM2877816: Primordial_follicle_B10ORO; Homo sapiens; RNA-Seq SRP126216 SRS2737123 GSM2877816 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877816 GSM2877816 GEO Accession GSM2877816 SRX3447171 GSM2877817 GSM2877817: Primordial_follicle_B14O; Homo sapiens; RNA-Seq SRP126216 SRS2737122 GSM2877817 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877817 GSM2877817 GEO Accession GSM2877817 SRX3447172 GSM2877818 GSM2877818: Primordial_follicle_B16O; Homo sapiens; RNA-Seq SRP126216 SRS2737125 GSM2877818 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877818 GSM2877818 GEO Accession GSM2877818 SRX3447173 GSM2877819 GSM2877819: Primordial_follicle_B26O; Homo sapiens; RNA-Seq SRP126216 SRS2737124 GSM2877819 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877819 GSM2877819 GEO Accession GSM2877819 SRX3447174 GSM2877820 GSM2877820: Primordial_follicle_B30O; Homo sapiens; RNA-Seq SRP126216 SRS2737126 GSM2877820 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877820 GSM2877820 GEO Accession GSM2877820 SRX3447175 GSM2877821 GSM2877821: Primordial_follicle_B32O; Homo sapiens; RNA-Seq SRP126216 SRS2737127 GSM2877821 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877821 GSM2877821 GEO Accession GSM2877821 SRX3447176 GSM2877822 GSM2877822: Primordial_follicle_B33ORO; Homo sapiens; RNA-Seq SRP126216 SRS2737128 GSM2877822 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877822 GSM2877822 GEO Accession GSM2877822 SRX3447177 GSM2877823 GSM2877823: Primordial_follicle_B5ORO; Homo sapiens; RNA-Seq SRP126216 SRS2737129 GSM2877823 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877823 GSM2877823 GEO Accession GSM2877823 SRX3447178 GSM2877824 GSM2877824: Primordial_follicle_B5O; Homo sapiens; RNA-Seq SRP126216 SRS2737130 GSM2877824 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877824 GSM2877824 GEO Accession GSM2877824 SRX3447179 GSM2877825 GSM2877825: Primordial_follicle_B8O; Homo sapiens; RNA-Seq SRP126216 SRS2737131 GSM2877825 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877825 GSM2877825 GEO Accession GSM2877825 SRX3447180 GSM2877826 GSM2877826: Primordial_follicle_F38O; Homo sapiens; RNA-Seq SRP126216 SRS2737132 GSM2877826 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877826 GSM2877826 GEO Accession GSM2877826 SRX3447181 GSM2877827 GSM2877827: Primordial_follicle_F39O; Homo sapiens; RNA-Seq SRP126216 SRS2737133 GSM2877827 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877827 GSM2877827 GEO Accession GSM2877827 SRX3447182 GSM2877828 GSM2877828: Primary_follicle_A11O; Homo sapiens; RNA-Seq SRP126216 SRS2737134 GSM2877828 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877828 GSM2877828 GEO Accession GSM2877828 SRX3447183 GSM2877829 GSM2877829: Primary_follicle_A17O; Homo sapiens; RNA-Seq SRP126216 SRS2737135 GSM2877829 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877829 GSM2877829 GEO Accession GSM2877829 SRX3447184 GSM2877830 GSM2877830: Primary_follicle_A18O; Homo sapiens; RNA-Seq SRP126216 SRS2737136 GSM2877830 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877830 GSM2877830 GEO Accession GSM2877830 SRX3447185 GSM2877831 GSM2877831: Primary_follicle_A19O; Homo sapiens; RNA-Seq SRP126216 SRS2737137 GSM2877831 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877831 GSM2877831 GEO Accession GSM2877831 SRX3447186 GSM2877832 GSM2877832: Primary_follicle_A20O; Homo sapiens; RNA-Seq SRP126216 SRS2737138 GSM2877832 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877832 GSM2877832 GEO Accession GSM2877832 SRX3447187 GSM2877833 GSM2877833: Primary_follicle_A2O; Homo sapiens; RNA-Seq SRP126216 SRS2737139 GSM2877833 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877833 GSM2877833 GEO Accession GSM2877833 SRX3447188 GSM2877834 GSM2877834: Primary_follicle_A3O; Homo sapiens; RNA-Seq SRP126216 SRS2737140 GSM2877834 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877834 GSM2877834 GEO Accession GSM2877834 SRX3447189 GSM2877835 GSM2877835: Primary_follicle_A5O; Homo sapiens; RNA-Seq SRP126216 SRS2737141 GSM2877835 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877835 GSM2877835 GEO Accession GSM2877835 SRX3447190 GSM2877836 GSM2877836: Primary_follicle_B10O; Homo sapiens; RNA-Seq SRP126216 SRS2737142 GSM2877836 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877836 GSM2877836 GEO Accession GSM2877836 SRX3447191 GSM2877837 GSM2877837: Primary_follicle_B11O; Homo sapiens; RNA-Seq SRP126216 SRS2737143 GSM2877837 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877837 GSM2877837 GEO Accession GSM2877837 SRX3447192 GSM2877838 GSM2877838: Primary_follicle_B13O; Homo sapiens; RNA-Seq SRP126216 SRS2737144 GSM2877838 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877838 GSM2877838 GEO Accession GSM2877838 SRX3447193 GSM2877839 GSM2877839: Primary_follicle_B16ORO; Homo sapiens; RNA-Seq SRP126216 SRS2737145 GSM2877839 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877839 GSM2877839 GEO Accession GSM2877839 SRX3447194 GSM2877840 GSM2877840: Primary_follicle_B18O; Homo sapiens; RNA-Seq SRP126216 SRS2737147 GSM2877840 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877840 GSM2877840 GEO Accession GSM2877840 SRX3447195 GSM2877841 GSM2877841: Primary_follicle_B1O; Homo sapiens; RNA-Seq SRP126216 SRS2737146 GSM2877841 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877841 GSM2877841 GEO Accession GSM2877841 SRX3447196 GSM2877842 GSM2877842: Primary_follicle_B20O; Homo sapiens; RNA-Seq SRP126216 SRS2737148 GSM2877842 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877842 GSM2877842 GEO Accession GSM2877842 SRX3447197 GSM2877843 GSM2877843: Primary_follicle_B25O; Homo sapiens; RNA-Seq SRP126216 SRS2737149 GSM2877843 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877843 GSM2877843 GEO Accession GSM2877843 SRX3447198 GSM2877844 GSM2877844: Primary_follicle_B27O; Homo sapiens; RNA-Seq SRP126216 SRS2737150 GSM2877844 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877844 GSM2877844 GEO Accession GSM2877844 SRX3447199 GSM2877845 GSM2877845: Primary_follicle_B28O; Homo sapiens; RNA-Seq SRP126216 SRS2737151 GSM2877845 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877845 GSM2877845 GEO Accession GSM2877845 SRX3447200 GSM2877846 GSM2877846: Primary_follicle_B2O; Homo sapiens; RNA-Seq SRP126216 SRS2737152 GSM2877846 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877846 GSM2877846 GEO Accession GSM2877846 SRX3447201 GSM2877847 GSM2877847: Primary_follicle_B33O; Homo sapiens; RNA-Seq SRP126216 SRS2737153 GSM2877847 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877847 GSM2877847 GEO Accession GSM2877847 SRX3447202 GSM2877848 GSM2877848: Primary_follicle_B35O; Homo sapiens; RNA-Seq SRP126216 SRS2737154 GSM2877848 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877848 GSM2877848 GEO Accession GSM2877848 SRX3447203 GSM2877849 GSM2877849: Primary_follicle_B3O; Homo sapiens; RNA-Seq SRP126216 SRS2737155 GSM2877849 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877849 GSM2877849 GEO Accession GSM2877849 SRX3447204 GSM2877850 GSM2877850: Primary_follicle_B6O; Homo sapiens; RNA-Seq SRP126216 SRS2737156 GSM2877850 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877850 GSM2877850 GEO Accession GSM2877850 SRX3447205 GSM2877851 GSM2877851: Primary_follicle_B7O; Homo sapiens; RNA-Seq SRP126216 SRS2737157 GSM2877851 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877851 GSM2877851 GEO Accession GSM2877851 SRX3447206 GSM2877852 GSM2877852: Primary_follicle_S8O; Homo sapiens; RNA-Seq SRP126216 SRS2737158 GSM2877852 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877852 GSM2877852 GEO Accession GSM2877852 SRX3447207 GSM2877853 GSM2877853: Secondary_follicle_F26O; Homo sapiens; RNA-Seq SRP126216 SRS2737159 GSM2877853 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877853 GSM2877853 GEO Accession GSM2877853 SRX3447208 GSM2877854 GSM2877854: Secondary_follicle_G1O; Homo sapiens; RNA-Seq SRP126216 SRS2737160 GSM2877854 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877854 GSM2877854 GEO Accession GSM2877854 SRX3447209 GSM2877855 GSM2877855: Secondary_follicle_G2.2O; Homo sapiens; RNA-Seq SRP126216 SRS2737161 GSM2877855 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877855 GSM2877855 GEO Accession GSM2877855 SRX3447210 GSM2877856 GSM2877856: Secondary_follicle_G2O; Homo sapiens; RNA-Seq SRP126216 SRS2737162 GSM2877856 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877856 GSM2877856 GEO Accession GSM2877856 SRX3447211 GSM2877857 GSM2877857: Secondary_follicle_G3.1O; Homo sapiens; RNA-Seq SRP126216 SRS2737163 GSM2877857 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877857 GSM2877857 GEO Accession GSM2877857 SRX3447212 GSM2877858 GSM2877858: Secondary_follicle_G4.2O; Homo sapiens; RNA-Seq SRP126216 SRS2737164 GSM2877858 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877858 GSM2877858 GEO Accession GSM2877858 SRX3447213 GSM2877859 GSM2877859: Secondary_follicle_G4O; Homo sapiens; RNA-Seq SRP126216 SRS2737165 GSM2877859 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877859 GSM2877859 GEO Accession GSM2877859 SRX3447214 GSM2877860 GSM2877860: Secondary_follicle_G5O; Homo sapiens; RNA-Seq SRP126216 SRS2737166 GSM2877860 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877860 GSM2877860 GEO Accession GSM2877860 SRX3447215 GSM2877861 GSM2877861: Secondary_follicle_G6.2O; Homo sapiens; RNA-Seq SRP126216 SRS2737167 GSM2877861 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877861 GSM2877861 GEO Accession GSM2877861 SRX3447216 GSM2877862 GSM2877862: Secondary_follicle_G6O; Homo sapiens; RNA-Seq SRP126216 SRS2737168 GSM2877862 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877862 GSM2877862 GEO Accession GSM2877862 SRX3447217 GSM2877863 GSM2877863: Secondary_follicle_G8O; Homo sapiens; RNA-Seq SRP126216 SRS2737169 GSM2877863 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877863 GSM2877863 GEO Accession GSM2877863 SRX3447218 GSM2877864 GSM2877864: Secondary_follicle_G9.2O; Homo sapiens; RNA-Seq SRP126216 SRS2737170 GSM2877864 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877864 GSM2877864 GEO Accession GSM2877864 SRX3447219 GSM2877865 GSM2877865: Antral_follicle_X10O; Homo sapiens; RNA-Seq SRP126216 SRS2737171 GSM2877865 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877865 GSM2877865 GEO Accession GSM2877865 SRX3447220 GSM2877866 GSM2877866: Antral_follicle_X16O; Homo sapiens; RNA-Seq SRP126216 SRS2737172 GSM2877866 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877866 GSM2877866 GEO Accession GSM2877866 SRX3447221 GSM2877867 GSM2877867: Antral_follicle_X17O; Homo sapiens; RNA-Seq SRP126216 SRS2737173 GSM2877867 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877867 GSM2877867 GEO Accession GSM2877867 SRX3447222 GSM2877868 GSM2877868: Antral_follicle_X18O; Homo sapiens; RNA-Seq SRP126216 SRS2737174 GSM2877868 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877868 GSM2877868 GEO Accession GSM2877868 SRX3447223 GSM2877869 GSM2877869: Antral_follicle_X19O; Homo sapiens; RNA-Seq SRP126216 SRS2737175 GSM2877869 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877869 GSM2877869 GEO Accession GSM2877869 SRX3447224 GSM2877870 GSM2877870: Antral_follicle_X21O; Homo sapiens; RNA-Seq SRP126216 SRS2737176 GSM2877870 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877870 GSM2877870 GEO Accession GSM2877870 SRX3447225 GSM2877871 GSM2877871: Antral_follicle_X22O; Homo sapiens; RNA-Seq SRP126216 SRS2737177 GSM2877871 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877871 GSM2877871 GEO Accession GSM2877871 SRX3447226 GSM2877872 GSM2877872: Antral_follicle_X23O; Homo sapiens; RNA-Seq SRP126216 SRS2737178 GSM2877872 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877872 GSM2877872 GEO Accession GSM2877872 SRX3447227 GSM2877873 GSM2877873: Antral_follicle_X27O; Homo sapiens; RNA-Seq SRP126216 SRS2737179 GSM2877873 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877873 GSM2877873 GEO Accession GSM2877873 SRX3447228 GSM2877874 GSM2877874: Antral_follicle_X29O; Homo sapiens; RNA-Seq SRP126216 SRS2737180 GSM2877874 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877874 GSM2877874 GEO Accession GSM2877874 SRX3447229 GSM2877875 GSM2877875: Antral_follicle_X30O; Homo sapiens; RNA-Seq SRP126216 SRS2737181 GSM2877875 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877875 GSM2877875 GEO Accession GSM2877875 SRX3447230 GSM2877876 GSM2877876: Antral_follicle_C1O; Homo sapiens; RNA-Seq SRP126216 SRS2737182 GSM2877876 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877876 GSM2877876 GEO Accession GSM2877876 SRX3447231 GSM2877877 GSM2877877: Antral_follicle_C4O; Homo sapiens; RNA-Seq SRP126216 SRS2737183 GSM2877877 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877877 GSM2877877 GEO Accession GSM2877877 SRX3447232 GSM2877878 GSM2877878: Antral_follicle_C5O; Homo sapiens; RNA-Seq SRP126216 SRS2737184 GSM2877878 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877878 GSM2877878 GEO Accession GSM2877878 SRX3447233 GSM2877879 GSM2877879: Antral_follicle_C8O; Homo sapiens; RNA-Seq SRP126216 SRS2737185 GSM2877879 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877879 GSM2877879 GEO Accession GSM2877879 SRX3447234 GSM2877880 GSM2877880: Antral_follicle_E1O; Homo sapiens; RNA-Seq SRP126216 SRS2737186 GSM2877880 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877880 GSM2877880 GEO Accession GSM2877880 SRX3447235 GSM2877881 GSM2877881: Antral_follicle_E4O; Homo sapiens; RNA-Seq SRP126216 SRS2737187 GSM2877881 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877881 GSM2877881 GEO Accession GSM2877881 SRX3447236 GSM2877882 GSM2877882: Antral_follicle_E5O; Homo sapiens; RNA-Seq SRP126216 SRS2737188 GSM2877882 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877882 GSM2877882 GEO Accession GSM2877882 SRX3447237 GSM2877883 GSM2877883: Antral_follicle_E9O; Homo sapiens; RNA-Seq SRP126216 SRS2737189 GSM2877883 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877883 GSM2877883 GEO Accession GSM2877883 SRX3447238 GSM2877884 GSM2877884: Antral_follicle_G3O; Homo sapiens; RNA-Seq SRP126216 SRS2737190 GSM2877884 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877884 GSM2877884 GEO Accession GSM2877884 SRX3447239 GSM2877885 GSM2877885: Antral_follicle_S12O; Homo sapiens; RNA-Seq SRP126216 SRS2737191 GSM2877885 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877885 GSM2877885 GEO Accession GSM2877885 SRX3447240 GSM2877886 GSM2877886: Antral_follicle_S25O; Homo sapiens; RNA-Seq SRP126216 SRS2737192 GSM2877886 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877886 GSM2877886 GEO Accession GSM2877886 SRX3447241 GSM2877887 GSM2877887: Antral_follicle_S26O; Homo sapiens; RNA-Seq SRP126216 SRS2737193 GSM2877887 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877887 GSM2877887 GEO Accession GSM2877887 SRX3447242 GSM2877888 GSM2877888: Primordial_follicle_A18G; Homo sapiens; RNA-Seq SRP126216 SRS2737194 GSM2877888 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877888 GSM2877888 GEO Accession GSM2877888 SRX3447243 GSM2877889 GSM2877889: Primordial_follicle_A3G; Homo sapiens; RNA-Seq SRP126216 SRS2737196 GSM2877889 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877889 GSM2877889 GEO Accession GSM2877889 SRX3447244 GSM2877890 GSM2877890: Primordial_follicle_A8G; Homo sapiens; RNA-Seq SRP126216 SRS2737195 GSM2877890 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877890 GSM2877890 GEO Accession GSM2877890 SRX3447245 GSM2877891 GSM2877891: Primordial_follicle_A9G; Homo sapiens; RNA-Seq SRP126216 SRS2737197 GSM2877891 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877891 GSM2877891 GEO Accession GSM2877891 SRX3447246 GSM2877892 GSM2877892: Primordial_follicle_B26G; Homo sapiens; RNA-Seq SRP126216 SRS2737198 GSM2877892 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877892 GSM2877892 GEO Accession GSM2877892 SRX3447247 GSM2877893 GSM2877893: Primordial_follicle_B2G; Homo sapiens; RNA-Seq SRP126216 SRS2737200 GSM2877893 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877893 GSM2877893 GEO Accession GSM2877893 SRX3447248 GSM2877894 GSM2877894: Primordial_follicle_B32G; Homo sapiens; RNA-Seq SRP126216 SRS2737199 GSM2877894 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877894 GSM2877894 GEO Accession GSM2877894 SRX3447249 GSM2877895 GSM2877895: Primordial_follicle_B35G; Homo sapiens; RNA-Seq SRP126216 SRS2737202 GSM2877895 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877895 GSM2877895 GEO Accession GSM2877895 SRX3447250 GSM2877896 GSM2877896: Primary_follicle_X17G; Homo sapiens; RNA-Seq SRP126216 SRS2737201 GSM2877896 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877896 GSM2877896 GEO Accession GSM2877896 SRX3447251 GSM2877897 GSM2877897: Primary_follicle_X30G; Homo sapiens; RNA-Seq SRP126216 SRS2737203 GSM2877897 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877897 GSM2877897 GEO Accession GSM2877897 SRX3447252 GSM2877898 GSM2877898: Primary_follicle_A11G; Homo sapiens; RNA-Seq SRP126216 SRS2737204 GSM2877898 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877898 GSM2877898 GEO Accession GSM2877898 SRX3447253 GSM2877899 GSM2877899: Primary_follicle_A14G; Homo sapiens; RNA-Seq SRP126216 SRS2737205 GSM2877899 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877899 GSM2877899 GEO Accession GSM2877899 SRX3447254 GSM2877900 GSM2877900: Primary_follicle_A5G; Homo sapiens; RNA-Seq SRP126216 SRS2737206 GSM2877900 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877900 GSM2877900 GEO Accession GSM2877900 SRX3447255 GSM2877901 GSM2877901: Primary_follicle_A7G; Homo sapiens; RNA-Seq SRP126216 SRS2737207 GSM2877901 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877901 GSM2877901 GEO Accession GSM2877901 SRX3447256 GSM2877902 GSM2877902: Primary_follicle_B11G; Homo sapiens; RNA-Seq SRP126216 SRS2737208 GSM2877902 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877902 GSM2877902 GEO Accession GSM2877902 SRX3447257 GSM2877903 GSM2877903: Primary_follicle_B13G; Homo sapiens; RNA-Seq SRP126216 SRS2737209 GSM2877903 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877903 GSM2877903 GEO Accession GSM2877903 SRX3447258 GSM2877904 GSM2877904: Primary_follicle_B1G; Homo sapiens; RNA-Seq SRP126216 SRS2737210 GSM2877904 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877904 GSM2877904 GEO Accession GSM2877904 SRX3447259 GSM2877905 GSM2877905: Primary_follicle_b23G; Homo sapiens; RNA-Seq SRP126216 SRS2737211 GSM2877905 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877905 GSM2877905 GEO Accession GSM2877905 SRX3447260 GSM2877906 GSM2877906: Primary_follicle_B24G; Homo sapiens; RNA-Seq SRP126216 SRS2737212 GSM2877906 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877906 GSM2877906 GEO Accession GSM2877906 SRX3447261 GSM2877907 GSM2877907: Primary_follicle_B25G; Homo sapiens; RNA-Seq SRP126216 SRS2737213 GSM2877907 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877907 GSM2877907 GEO Accession GSM2877907 SRX3447262 GSM2877908 GSM2877908: Primary_follicle_B27G; Homo sapiens; RNA-Seq SRP126216 SRS2737214 GSM2877908 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877908 GSM2877908 GEO Accession GSM2877908 SRX3447263 GSM2877909 GSM2877909: Primary_follicle_B3G; Homo sapiens; RNA-Seq SRP126216 SRS2737215 GSM2877909 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877909 GSM2877909 GEO Accession GSM2877909 SRX3447264 GSM2877910 GSM2877910: Primary_follicle_B7G; Homo sapiens; RNA-Seq SRP126216 SRS2737216 GSM2877910 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877910 GSM2877910 GEO Accession GSM2877910 SRX3447265 GSM2877911 GSM2877911: Secondary_follicle_B33G; Homo sapiens; RNA-Seq SRP126216 SRS2737217 GSM2877911 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877911 GSM2877911 GEO Accession GSM2877911 SRX3447266 GSM2877912 GSM2877912: Secondary_follicle_C3G; Homo sapiens; RNA-Seq SRP126216 SRS2737218 GSM2877912 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877912 GSM2877912 GEO Accession GSM2877912 SRX3447267 GSM2877913 GSM2877913: Secondary_follicle_E1G; Homo sapiens; RNA-Seq SRP126216 SRS2737219 GSM2877913 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877913 GSM2877913 GEO Accession GSM2877913 SRX3447268 GSM2877914 GSM2877914: Secondary_follicle_G4G; Homo sapiens; RNA-Seq SRP126216 SRS2737220 GSM2877914 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877914 GSM2877914 GEO Accession GSM2877914 SRX3447269 GSM2877915 GSM2877915: Secondary_follicle_G8G; Homo sapiens; RNA-Seq SRP126216 SRS2737221 GSM2877915 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877915 GSM2877915 GEO Accession GSM2877915 SRX3447270 GSM2877916 GSM2877916: Secondary_follicle_G9G; Homo sapiens; RNA-Seq SRP126216 SRS2737222 GSM2877916 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877916 GSM2877916 GEO Accession GSM2877916 SRX3447271 GSM2877917 GSM2877917: Antral_follicle_X10G; Homo sapiens; RNA-Seq SRP126216 SRS2737223 GSM2877917 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877917 GSM2877917 GEO Accession GSM2877917 SRX3447272 GSM2877918 GSM2877918: Antral_follicle_X20G; Homo sapiens; RNA-Seq SRP126216 SRS2737224 GSM2877918 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877918 GSM2877918 GEO Accession GSM2877918 SRX3447273 GSM2877919 GSM2877919: Antral_follicle_X21G; Homo sapiens; RNA-Seq SRP126216 SRS2737226 GSM2877919 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877919 GSM2877919 GEO Accession GSM2877919 SRX3447274 GSM2877920 GSM2877920: Antral_follicle_X26G; Homo sapiens; RNA-Seq SRP126216 SRS2737225 GSM2877920 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877920 GSM2877920 GEO Accession GSM2877920 SRX3447275 GSM2877921 GSM2877921: Antral_follicle_X28G; Homo sapiens; RNA-Seq SRP126216 SRS2737228 GSM2877921 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877921 GSM2877921 GEO Accession GSM2877921 SRX3447276 GSM2877922 GSM2877922: Antral_follicle_X4.2G; Homo sapiens; RNA-Seq SRP126216 SRS2737227 GSM2877922 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877922 GSM2877922 GEO Accession GSM2877922 SRX3447277 GSM2877923 GSM2877923: Antral_follicle_X4G; Homo sapiens; RNA-Seq SRP126216 SRS2737229 GSM2877923 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877923 GSM2877923 GEO Accession GSM2877923 SRX3447278 GSM2877924 GSM2877924: Antral_follicle_X9G; Homo sapiens; RNA-Seq SRP126216 SRS2737230 GSM2877924 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877924 GSM2877924 GEO Accession GSM2877924 SRX3447279 GSM2877925 GSM2877925: Antral_follicle_C1G1G; Homo sapiens; RNA-Seq SRP126216 SRS2737231 GSM2877925 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877925 GSM2877925 GEO Accession GSM2877925 SRX3447280 GSM2877926 GSM2877926: Antral_follicle_C1G2G; Homo sapiens; RNA-Seq SRP126216 SRS2737232 GSM2877926 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877926 GSM2877926 GEO Accession GSM2877926 SRX3447281 GSM2877927 GSM2877927: Antral_follicle_C1M1G; Homo sapiens; RNA-Seq SRP126216 SRS2737233 GSM2877927 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877927 GSM2877927 GEO Accession GSM2877927 SRX3447282 GSM2877928 GSM2877928: Antral_follicle_C2CG1G; Homo sapiens; RNA-Seq SRP126216 SRS2737234 GSM2877928 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877928 GSM2877928 GEO Accession GSM2877928 SRX3447283 GSM2877929 GSM2877929: Antral_follicle_C2CG2G; Homo sapiens; RNA-Seq SRP126216 SRS2737235 GSM2877929 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877929 GSM2877929 GEO Accession GSM2877929 SRX3447284 GSM2877930 GSM2877930: Antral_follicle_C4GC2G; Homo sapiens; RNA-Seq SRP126216 SRS2737236 GSM2877930 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877930 GSM2877930 GEO Accession GSM2877930 SRX3447285 GSM2877931 GSM2877931: Antral_follicle_C4M1G; Homo sapiens; RNA-Seq SRP126216 SRS2737237 GSM2877931 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877931 GSM2877931 GEO Accession GSM2877931 SRX3447286 GSM2877932 GSM2877932: Antral_follicle_C4M2G; Homo sapiens; RNA-Seq SRP126216 SRS2737238 GSM2877932 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877932 GSM2877932 GEO Accession GSM2877932 SRX3447287 GSM2877933 GSM2877933: Antral_follicle_C6C1G; Homo sapiens; RNA-Seq SRP126216 SRS2737239 GSM2877933 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877933 GSM2877933 GEO Accession GSM2877933 SRX3447288 GSM2877934 GSM2877934: Antral_follicle_C6C2G; Homo sapiens; RNA-Seq SRP126216 SRS2737240 GSM2877934 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877934 GSM2877934 GEO Accession GSM2877934 SRX3447289 GSM2877935 GSM2877935: Antral_follicle_C8C2G; Homo sapiens; RNA-Seq SRP126216 SRS2737241 GSM2877935 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877935 GSM2877935 GEO Accession GSM2877935 SRX3447290 GSM2877936 GSM2877936: Antral_follicle_C8G; Homo sapiens; RNA-Seq SRP126216 SRS2737242 GSM2877936 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877936 GSM2877936 GEO Accession GSM2877936 SRX3447291 GSM2877937 GSM2877937: Antral_follicle_C8G2G; Homo sapiens; RNA-Seq SRP126216 SRS2737243 GSM2877937 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877937 GSM2877937 GEO Accession GSM2877937 SRX3447292 GSM2877938 GSM2877938: Antral_follicle_S12G; Homo sapiens; RNA-Seq SRP126216 SRS2737244 GSM2877938 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877938 GSM2877938 GEO Accession GSM2877938 SRX3447293 GSM2877939 GSM2877939: Antral_follicle_S25G; Homo sapiens; RNA-Seq SRP126216 SRS2737245 GSM2877939 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877939 GSM2877939 GEO Accession GSM2877939 SRX3447294 GSM2877940 GSM2877940: Antral_follicle_S29G; Homo sapiens; RNA-Seq SRP126216 SRS2737246 GSM2877940 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877940 GSM2877940 GEO Accession GSM2877940 SRX3447295 GSM2877941 GSM2877941: Preovulatory_follicle_G1.1M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737248 GSM2877941 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877941 GSM2877941 GEO Accession GSM2877941 SRX3447296 GSM2877942 GSM2877942: Preovulatory_follicle_G1.2M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737247 GSM2877942 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877942 GSM2877942 GEO Accession GSM2877942 SRX3447297 GSM2877943 GSM2877943: Preovulatory_follicle_G1.3M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737249 GSM2877943 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877943 GSM2877943 GEO Accession GSM2877943 SRX3447298 GSM2877944 GSM2877944: Preovulatory_follicle_G2.1M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737250 GSM2877944 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877944 GSM2877944 GEO Accession GSM2877944 SRX3447299 GSM2877945 GSM2877945: Preovulatory_follicle_G2.2M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737251 GSM2877945 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877945 GSM2877945 GEO Accession GSM2877945 SRX3447300 GSM2877946 GSM2877946: Preovulatory_follicle_G2.3M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737252 GSM2877946 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877946 GSM2877946 GEO Accession GSM2877946 SRX3447301 GSM2877947 GSM2877947: Preovulatory_follicle_G3.1M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737253 GSM2877947 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877947 GSM2877947 GEO Accession GSM2877947 SRX3447302 GSM2877948 GSM2877948: Preovulatory_follicle_G3.2M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737254 GSM2877948 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877948 GSM2877948 GEO Accession GSM2877948 SRX3447303 GSM2877949 GSM2877949: Preovulatory_follicle_G3.3M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737255 GSM2877949 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877949 GSM2877949 GEO Accession GSM2877949 SRX3447304 GSM2877950 GSM2877950: Preovulatory_follicle_G4.1M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737256 GSM2877950 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877950 GSM2877950 GEO Accession GSM2877950 SRX3447305 GSM2877951 GSM2877951: Preovulatory_follicle_G4.2M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737257 GSM2877951 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877951 GSM2877951 GEO Accession GSM2877951 SRX3447306 GSM2877952 GSM2877952: Preovulatory_follicle_G4.3M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737258 GSM2877952 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877952 GSM2877952 GEO Accession GSM2877952 SRX3447307 GSM2877953 GSM2877953: Preovulatory_follicle_G5.1M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737259 GSM2877953 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877953 GSM2877953 GEO Accession GSM2877953 SRX3447308 GSM2877954 GSM2877954: Preovulatory_follicle_G5.2M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737260 GSM2877954 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877954 GSM2877954 GEO Accession GSM2877954 SRX3447309 GSM2877955 GSM2877955: Preovulatory_follicle_G5.3M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737261 GSM2877955 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877955 GSM2877955 GEO Accession GSM2877955 SRX3447310 GSM2877956 GSM2877956: Preovulatory_follicle_G6.1M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737262 GSM2877956 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877956 GSM2877956 GEO Accession GSM2877956 SRX3447311 GSM2877957 GSM2877957: Preovulatory_follicle_G6.2M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737263 GSM2877957 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877957 GSM2877957 GEO Accession GSM2877957 SRX3447312 GSM2877958 GSM2877958: Preovulatory_follicle_G6.3M.G; Homo sapiens; RNA-Seq SRP126216 SRS2737264 GSM2877958 RNA-Seq TRANSCRIPTOMIC cDNA Each oocyte and 10 randomly selected granulosa cells were transferred into lysis buffer using a mouth pipette. The reverse transcription reaction was performed on the whole-cell lysate and terminal deoxynucleotidyl transferase was used to add a poly A tail to the 3′ end of the first-strand cDNAs, and then 20 cycles of PCR were performed to amplify the single-cell cDNA RNA libraries were prepared according to instructions of Kappa Hyper Prep Kit (Kappa Biosystems). HiSeq X Ten gds 302877958 GSM2877958 GEO Accession GSM2877958