SRX6777803 GSM4052297 SRP178920 PRJNA514925 SRS5324754 GSM4052297 RNA-Seq TRANSCRIPTOMIC cDNA Normal ovary and fallopian tube (fimbriae) were embedded in FSC 22 Clear Frozen Section Compound and immediately frozen with liquid N2. The resultant blocks were cut at 5-8 μm and mounted on a PEN membrane frame (Leica), followed by air-drying the slides for 30 minutes at room temperature. Laser capture was performed with a Leica LMD6000 laser microdissection system, and excised pieces were harvested into 200 μl RNase-free tubes, which were carefully recovered from the microscope, centrifuged, and placed on ice. Ovarian tumors (T-O) were from LPT organoid implants, and fallopian tube tumors were (T-FT) from PTPT organoid implants, all at 6 months post-injection. RNA was extracted by using the miRNeasy mini Kit (Qiagen), following the manufacturer's instruction. Libraries were prepared using the Illumina TruSeq Stranded Total RNA Sample Preparation Kit. Illumina HiSeq 4000 gds 304052297 GSM4052297 GEO Accession GSM4052297 SRX6777804 GSM4052298 SRP178920 PRJNA514925 SRS5324755 GSM4052298 RNA-Seq TRANSCRIPTOMIC cDNA Normal ovary and fallopian tube (fimbriae) were embedded in FSC 22 Clear Frozen Section Compound and immediately frozen with liquid N2. The resultant blocks were cut at 5-8 μm and mounted on a PEN membrane frame (Leica), followed by air-drying the slides for 30 minutes at room temperature. Laser capture was performed with a Leica LMD6000 laser microdissection system, and excised pieces were harvested into 200 μl RNase-free tubes, which were carefully recovered from the microscope, centrifuged, and placed on ice. Ovarian tumors (T-O) were from LPT organoid implants, and fallopian tube tumors were (T-FT) from PTPT organoid implants, all at 6 months post-injection. RNA was extracted by using the miRNeasy mini Kit (Qiagen), following the manufacturer's instruction. Libraries were prepared using the Illumina TruSeq Stranded Total RNA Sample Preparation Kit. Illumina HiSeq 4000 gds 304052298 GSM4052298 GEO Accession GSM4052298 SRX6777805 GSM4052299 SRP178920 PRJNA514925 SRS5324756 GSM4052299 RNA-Seq TRANSCRIPTOMIC cDNA Normal ovary and fallopian tube (fimbriae) were embedded in FSC 22 Clear Frozen Section Compound and immediately frozen with liquid N2. The resultant blocks were cut at 5-8 μm and mounted on a PEN membrane frame (Leica), followed by air-drying the slides for 30 minutes at room temperature. Laser capture was performed with a Leica LMD6000 laser microdissection system, and excised pieces were harvested into 200 μl RNase-free tubes, which were carefully recovered from the microscope, centrifuged, and placed on ice. Ovarian tumors (T-O) were from LPT organoid implants, and fallopian tube tumors were (T-FT) from PTPT organoid implants, all at 6 months post-injection. RNA was extracted by using the miRNeasy mini Kit (Qiagen), following the manufacturer's instruction. Libraries were prepared using the Illumina TruSeq Stranded Total RNA Sample Preparation Kit. Illumina HiSeq 4000 gds 304052299 GSM4052299 GEO Accession GSM4052299 SRX6777806 GSM4052300 SRP178920 PRJNA514925 SRS5324757 GSM4052300 RNA-Seq TRANSCRIPTOMIC cDNA Normal ovary and fallopian tube (fimbriae) were embedded in FSC 22 Clear Frozen Section Compound and immediately frozen with liquid N2. The resultant blocks were cut at 5-8 μm and mounted on a PEN membrane frame (Leica), followed by air-drying the slides for 30 minutes at room temperature. Laser capture was performed with a Leica LMD6000 laser microdissection system, and excised pieces were harvested into 200 μl RNase-free tubes, which were carefully recovered from the microscope, centrifuged, and placed on ice. Ovarian tumors (T-O) were from LPT organoid implants, and fallopian tube tumors were (T-FT) from PTPT organoid implants, all at 6 months post-injection. RNA was extracted by using the miRNeasy mini Kit (Qiagen), following the manufacturer's instruction. Libraries were prepared using the Illumina TruSeq Stranded Total RNA Sample Preparation Kit. Illumina HiSeq 4000 gds 304052300 GSM4052300 GEO Accession GSM4052300 SRX6777807 GSM4052301 SRP178920 PRJNA514925 SRS5324758 GSM4052301 RNA-Seq TRANSCRIPTOMIC cDNA Normal ovary and fallopian tube (fimbriae) were embedded in FSC 22 Clear Frozen Section Compound and immediately frozen with liquid N2. The resultant blocks were cut at 5-8 μm and mounted on a PEN membrane frame (Leica), followed by air-drying the slides for 30 minutes at room temperature. Laser capture was performed with a Leica LMD6000 laser microdissection system, and excised pieces were harvested into 200 μl RNase-free tubes, which were carefully recovered from the microscope, centrifuged, and placed on ice. Ovarian tumors (T-O) were from LPT organoid implants, and fallopian tube tumors were (T-FT) from PTPT organoid implants, all at 6 months post-injection. RNA was extracted by using the miRNeasy mini Kit (Qiagen), following the manufacturer's instruction. Libraries were prepared using the Illumina TruSeq Stranded Total RNA Sample Preparation Kit. Illumina HiSeq 4000 gds 304052301 GSM4052301 GEO Accession GSM4052301 SRX6777808 GSM4052302 SRP178920 PRJNA514925 SRS5324759 GSM4052302 RNA-Seq TRANSCRIPTOMIC cDNA Normal ovary and fallopian tube (fimbriae) were embedded in FSC 22 Clear Frozen Section Compound and immediately frozen with liquid N2. The resultant blocks were cut at 5-8 μm and mounted on a PEN membrane frame (Leica), followed by air-drying the slides for 30 minutes at room temperature. Laser capture was performed with a Leica LMD6000 laser microdissection system, and excised pieces were harvested into 200 μl RNase-free tubes, which were carefully recovered from the microscope, centrifuged, and placed on ice. Ovarian tumors (T-O) were from LPT organoid implants, and fallopian tube tumors were (T-FT) from PTPT organoid implants, all at 6 months post-injection. RNA was extracted by using the miRNeasy mini Kit (Qiagen), following the manufacturer's instruction. Libraries were prepared using the Illumina TruSeq Stranded Total RNA Sample Preparation Kit. Illumina HiSeq 4000 gds 304052302 GSM4052302 GEO Accession GSM4052302 SRX6777809 GSM4052303 SRP178920 PRJNA514925 SRS5324760 GSM4052303 RNA-Seq TRANSCRIPTOMIC cDNA Normal ovary and fallopian tube (fimbriae) were embedded in FSC 22 Clear Frozen Section Compound and immediately frozen with liquid N2. The resultant blocks were cut at 5-8 μm and mounted on a PEN membrane frame (Leica), followed by air-drying the slides for 30 minutes at room temperature. Laser capture was performed with a Leica LMD6000 laser microdissection system, and excised pieces were harvested into 200 μl RNase-free tubes, which were carefully recovered from the microscope, centrifuged, and placed on ice. Ovarian tumors (T-O) were from LPT organoid implants, and fallopian tube tumors were (T-FT) from PTPT organoid implants, all at 6 months post-injection. RNA was extracted by using the miRNeasy mini Kit (Qiagen), following the manufacturer's instruction. Libraries were prepared using the Illumina TruSeq Stranded Total RNA Sample Preparation Kit. Illumina HiSeq 4000 gds 304052303 GSM4052303 GEO Accession GSM4052303 SRX6777810 GSM4052304 SRP178920 PRJNA514925 SRS5324761 GSM4052304 RNA-Seq TRANSCRIPTOMIC cDNA Normal ovary and fallopian tube (fimbriae) were embedded in FSC 22 Clear Frozen Section Compound and immediately frozen with liquid N2. The resultant blocks were cut at 5-8 μm and mounted on a PEN membrane frame (Leica), followed by air-drying the slides for 30 minutes at room temperature. Laser capture was performed with a Leica LMD6000 laser microdissection system, and excised pieces were harvested into 200 μl RNase-free tubes, which were carefully recovered from the microscope, centrifuged, and placed on ice. Ovarian tumors (T-O) were from LPT organoid implants, and fallopian tube tumors were (T-FT) from PTPT organoid implants, all at 6 months post-injection. RNA was extracted by using the miRNeasy mini Kit (Qiagen), following the manufacturer's instruction. Libraries were prepared using the Illumina TruSeq Stranded Total RNA Sample Preparation Kit. Illumina HiSeq 4000 gds 304052304 GSM4052304 GEO Accession GSM4052304 SRX6777811 GSM4052305 SRP178920 PRJNA514925 SRS5324762 GSM4052305 RNA-Seq TRANSCRIPTOMIC cDNA Normal ovary and fallopian tube (fimbriae) were embedded in FSC 22 Clear Frozen Section Compound and immediately frozen with liquid N2. The resultant blocks were cut at 5-8 μm and mounted on a PEN membrane frame (Leica), followed by air-drying the slides for 30 minutes at room temperature. Laser capture was performed with a Leica LMD6000 laser microdissection system, and excised pieces were harvested into 200 μl RNase-free tubes, which were carefully recovered from the microscope, centrifuged, and placed on ice. Ovarian tumors (T-O) were from LPT organoid implants, and fallopian tube tumors were (T-FT) from PTPT organoid implants, all at 6 months post-injection. RNA was extracted by using the miRNeasy mini Kit (Qiagen), following the manufacturer's instruction. Libraries were prepared using the Illumina TruSeq Stranded Total RNA Sample Preparation Kit. Illumina HiSeq 4000 gds 304052305 GSM4052305 GEO Accession GSM4052305 SRX6777812 GSM4052306 SRP178920 PRJNA514925 SRS5324763 GSM4052306 RNA-Seq TRANSCRIPTOMIC cDNA Normal ovary and fallopian tube (fimbriae) were embedded in FSC 22 Clear Frozen Section Compound and immediately frozen with liquid N2. The resultant blocks were cut at 5-8 μm and mounted on a PEN membrane frame (Leica), followed by air-drying the slides for 30 minutes at room temperature. Laser capture was performed with a Leica LMD6000 laser microdissection system, and excised pieces were harvested into 200 μl RNase-free tubes, which were carefully recovered from the microscope, centrifuged, and placed on ice. Ovarian tumors (T-O) were from LPT organoid implants, and fallopian tube tumors were (T-FT) from PTPT organoid implants, all at 6 months post-injection. RNA was extracted by using the miRNeasy mini Kit (Qiagen), following the manufacturer's instruction. Libraries were prepared using the Illumina TruSeq Stranded Total RNA Sample Preparation Kit. Illumina HiSeq 4000 gds 304052306 GSM4052306 GEO Accession GSM4052306 SRX6777813 GSM4052307 SRP178920 PRJNA514925 SRS5324764 GSM4052307 RNA-Seq TRANSCRIPTOMIC cDNA Normal ovary and fallopian tube (fimbriae) were embedded in FSC 22 Clear Frozen Section Compound and immediately frozen with liquid N2. The resultant blocks were cut at 5-8 μm and mounted on a PEN membrane frame (Leica), followed by air-drying the slides for 30 minutes at room temperature. Laser capture was performed with a Leica LMD6000 laser microdissection system, and excised pieces were harvested into 200 μl RNase-free tubes, which were carefully recovered from the microscope, centrifuged, and placed on ice. Ovarian tumors (T-O) were from LPT organoid implants, and fallopian tube tumors were (T-FT) from PTPT organoid implants, all at 6 months post-injection. RNA was extracted by using the miRNeasy mini Kit (Qiagen), following the manufacturer's instruction. Libraries were prepared using the Illumina TruSeq Stranded Total RNA Sample Preparation Kit. Illumina HiSeq 4000 gds 304052307 GSM4052307 GEO Accession GSM4052307 SRX6777814 GSM4052308 SRP178920 PRJNA514925 SRS5324765 GSM4052308 RNA-Seq TRANSCRIPTOMIC cDNA Normal ovary and fallopian tube (fimbriae) were embedded in FSC 22 Clear Frozen Section Compound and immediately frozen with liquid N2. The resultant blocks were cut at 5-8 μm and mounted on a PEN membrane frame (Leica), followed by air-drying the slides for 30 minutes at room temperature. Laser capture was performed with a Leica LMD6000 laser microdissection system, and excised pieces were harvested into 200 μl RNase-free tubes, which were carefully recovered from the microscope, centrifuged, and placed on ice. Ovarian tumors (T-O) were from LPT organoid implants, and fallopian tube tumors were (T-FT) from PTPT organoid implants, all at 6 months post-injection. RNA was extracted by using the miRNeasy mini Kit (Qiagen), following the manufacturer's instruction. Libraries were prepared using the Illumina TruSeq Stranded Total RNA Sample Preparation Kit. Illumina HiSeq 4000 gds 304052308 GSM4052308 GEO Accession GSM4052308 SRX6777815 GSM4052309 SRP178920 PRJNA514925 SRS5324766 GSM4052309 RNA-Seq TRANSCRIPTOMIC cDNA Normal ovary and fallopian tube (fimbriae) were embedded in FSC 22 Clear Frozen Section Compound and immediately frozen with liquid N2. The resultant blocks were cut at 5-8 μm and mounted on a PEN membrane frame (Leica), followed by air-drying the slides for 30 minutes at room temperature. Laser capture was performed with a Leica LMD6000 laser microdissection system, and excised pieces were harvested into 200 μl RNase-free tubes, which were carefully recovered from the microscope, centrifuged, and placed on ice. Ovarian tumors (T-O) were from LPT organoid implants, and fallopian tube tumors were (T-FT) from PTPT organoid implants, all at 6 months post-injection. RNA was extracted by using the miRNeasy mini Kit (Qiagen), following the manufacturer's instruction. Libraries were prepared using the Illumina TruSeq Stranded Total RNA Sample Preparation Kit. Illumina HiSeq 4000 gds 304052309 GSM4052309 GEO Accession GSM4052309 SRX6777816 GSM4052310 SRP178920 PRJNA514925 SRS5324767 GSM4052310 RNA-Seq TRANSCRIPTOMIC cDNA Normal ovary and fallopian tube (fimbriae) were embedded in FSC 22 Clear Frozen Section Compound and immediately frozen with liquid N2. The resultant blocks were cut at 5-8 μm and mounted on a PEN membrane frame (Leica), followed by air-drying the slides for 30 minutes at room temperature. Laser capture was performed with a Leica LMD6000 laser microdissection system, and excised pieces were harvested into 200 μl RNase-free tubes, which were carefully recovered from the microscope, centrifuged, and placed on ice. Ovarian tumors (T-O) were from LPT organoid implants, and fallopian tube tumors were (T-FT) from PTPT organoid implants, all at 6 months post-injection. RNA was extracted by using the miRNeasy mini Kit (Qiagen), following the manufacturer's instruction. Libraries were prepared using the Illumina TruSeq Stranded Total RNA Sample Preparation Kit. Illumina HiSeq 4000 gds 304052310 GSM4052310 GEO Accession GSM4052310