SRX11436662 GSM5451739 SRP328210 SRS9479348 GSM5451739 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were depellucidated using protease from Streptomyces griseus treatment and gentle mechanical dissociation. Cell singularization was achieved using trypsine 2 %, TryPLE 1 %, and gentle mechanical dissociation. Cell suspensions were loaded on a Chromium controller (10x Genomics, Pleasanton, CA, USA) to generate single-cell Gel Beads-in-Emulsion (GEMs). Single-cell RNA-Seq libraries were prepared using Chromium Single cell 3'RNA Gel Bead and Library Kit Illumina HiSeq 2500 gds 305451739 GSM5451739 GEO Accession GSM5451739 SRX11436663 GSM5451740 SRP328210 SRS9479349 GSM5451740 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were depellucidated using protease from Streptomyces griseus treatment and gentle mechanical dissociation. Cell singularization was achieved using trypsine 2 %, TryPLE 1 %, and gentle mechanical dissociation. Cell suspensions were loaded on a Chromium controller (10x Genomics, Pleasanton, CA, USA) to generate single-cell Gel Beads-in-Emulsion (GEMs). Single-cell RNA-Seq libraries were prepared using Chromium Single cell 3'RNA Gel Bead and Library Kit Illumina HiSeq 2500 gds 305451740 GSM5451740 GEO Accession GSM5451740 SRX11436664 GSM5451741 SRP328210 SRS9479350 GSM5451741 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were depellucidated using protease from Streptomyces griseus treatment and gentle mechanical dissociation. Cell singularization was achieved using trypsine 2 %, TryPLE 1 %, and gentle mechanical dissociation. Cell suspensions were loaded on a Chromium controller (10x Genomics, Pleasanton, CA, USA) to generate single-cell Gel Beads-in-Emulsion (GEMs). Single-cell RNA-Seq libraries were prepared using Chromium Single cell 3'RNA Gel Bead and Library Kit Illumina HiSeq 2500 gds 305451741 GSM5451741 GEO Accession GSM5451741 SRX11436665 GSM5451742 SRP328210 SRS9479351 GSM5451742 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were depellucidated using protease from Streptomyces griseus treatment and gentle mechanical dissociation. Cell singularization was achieved using trypsine 2 %, TryPLE 1 %, and gentle mechanical dissociation. Cell suspensions were loaded on a Chromium controller (10x Genomics, Pleasanton, CA, USA) to generate single-cell Gel Beads-in-Emulsion (GEMs). Single-cell RNA-Seq libraries were prepared using Chromium Single cell 3'RNA Gel Bead and Library Kit Illumina HiSeq 2500 gds 305451742 GSM5451742 GEO Accession GSM5451742 SRX11436666 GSM5451744 SRP328210 SRS9479352 GSM5451744 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were depellucidated using protease from Streptomyces griseus treatment and gentle mechanical dissociation. Cell singularization was achieved using trypsine 2 %, TryPLE 1 %, and gentle mechanical dissociation. Cell suspensions were loaded on a Chromium controller (10x Genomics, Pleasanton, CA, USA) to generate single-cell Gel Beads-in-Emulsion (GEMs). Single-cell RNA-Seq libraries were prepared using Chromium Single cell 3'RNA Gel Bead and Library Kit Illumina HiSeq 2500 gds 305451744 GSM5451744 GEO Accession GSM5451744 SRX11436667 GSM5451745 SRP328210 SRS9479353 GSM5451745 RNA-Seq TRANSCRIPTOMIC cDNA The embryos were depellucidated using protease from Streptomyces griseus treatment and gentle mechanical dissociation. Cell singularization was achieved using trypsine 2 %, TryPLE 1 %, and gentle mechanical dissociation. Cell suspensions were loaded on a Chromium controller (10x Genomics, Pleasanton, CA, USA) to generate single-cell Gel Beads-in-Emulsion (GEMs). Single-cell RNA-Seq libraries were prepared using Chromium Single cell 3'RNA Gel Bead and Library Kit Illumina HiSeq 2500 gds 305451745 GSM5451745 GEO Accession GSM5451745