SRX12683375 GSM5631871 SRP342075 SRS10634490 GSM5631871 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631871 GSM5631871 GEO Accession GSM5631871 SRX12683376 GSM5631872 SRP342075 SRS10634488 GSM5631872 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631872 GSM5631872 GEO Accession GSM5631872 SRX12683377 GSM5631873 SRP342075 SRS10634493 GSM5631873 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631873 GSM5631873 GEO Accession GSM5631873 SRX12683378 GSM5631874 SRP342075 SRS10634491 GSM5631874 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631874 GSM5631874 GEO Accession GSM5631874 SRX12683379 GSM5631875 SRP342075 SRS10634489 GSM5631875 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631875 GSM5631875 GEO Accession GSM5631875 SRX12683380 GSM5631876 SRP342075 SRS10634492 GSM5631876 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631876 GSM5631876 GEO Accession GSM5631876 SRX12683381 GSM5631855 SRP342075 SRS10634494 GSM5631855 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631855 GSM5631855 GEO Accession GSM5631855 SRX12683382 GSM5631856 SRP342075 SRS10634495 GSM5631856 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631856 GSM5631856 GEO Accession GSM5631856 SRX12683383 GSM5631857 SRP342075 SRS10634496 GSM5631857 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631857 GSM5631857 GEO Accession GSM5631857 SRX12683384 GSM5631858 SRP342075 SRS10634497 GSM5631858 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631858 GSM5631858 GEO Accession GSM5631858 SRX12683385 GSM5631859 SRP342075 SRS10634498 GSM5631859 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631859 GSM5631859 GEO Accession GSM5631859 SRX12683386 GSM5631860 SRP342075 SRS10634499 GSM5631860 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631860 GSM5631860 GEO Accession GSM5631860 SRX12683387 GSM5631861 SRP342075 SRS10634501 GSM5631861 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631861 GSM5631861 GEO Accession GSM5631861 SRX12683388 GSM5631862 SRP342075 SRS10634500 GSM5631862 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631862 GSM5631862 GEO Accession GSM5631862 SRX12683389 GSM5631863 SRP342075 SRS10634502 GSM5631863 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631863 GSM5631863 GEO Accession GSM5631863 SRX12683390 GSM5631864 SRP342075 SRS10634503 GSM5631864 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631864 GSM5631864 GEO Accession GSM5631864 SRX12683391 GSM5631865 SRP342075 SRS10634504 GSM5631865 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631865 GSM5631865 GEO Accession GSM5631865 SRX12683392 GSM5631866 SRP342075 SRS10634505 GSM5631866 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631866 GSM5631866 GEO Accession GSM5631866 SRX12683393 GSM5631867 SRP342075 SRS10634506 GSM5631867 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631867 GSM5631867 GEO Accession GSM5631867 SRX12683394 GSM5631868 SRP342075 SRS10634508 GSM5631868 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631868 GSM5631868 GEO Accession GSM5631868 SRX12683395 GSM5631869 SRP342075 SRS10634507 GSM5631869 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631869 GSM5631869 GEO Accession GSM5631869 SRX12683396 GSM5631870 SRP342075 SRS10634509 GSM5631870 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631870 GSM5631870 GEO Accession GSM5631870 SRX12683397 GSM5631853 SRP342075 SRS10634510 GSM5631853 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631853 GSM5631853 GEO Accession GSM5631853 SRX12683398 GSM5631854 SRP342075 SRS10634511 GSM5631854 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was purified from mouse hippocampi tissues using Isogen II reagent (Nippon Gene). Intact poly(A) RNA was purified from 1 µg of total RNA using an NEBNext® Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, USA) and following the manufacturer's protocol. Library preparation was performed using NEBNext® Ultra II Directional RNA Library Prep Kits for Illumina (New England Biolabs, USA), according to the manufacturer's protocol with 8 PCR cycles. Library sizes were checked using microfluidic-based electrophoresis LabChip GX Touch (Perkin Elmer, USA) and concentrations were checked using Qubit 1X dsDNA HS (ThermoFisher, USA) and then pooled after concentration adjustment. 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA). Illumina NovaSeq 6000 gds 305631854 GSM5631854 GEO Accession GSM5631854