SRX23809546 GSM8121909_r1 SRP492800 PRJNA1082635 SRS20632426 GSM8121909 GSM8121909 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Fresh full thickness human uterus samples obtained both during surgery for benign indications and from organ donors were used as tissue sources. When possible, the whole tissue sample was dissected into two anatomic segments (endometrium, myometrium). These segments separately were used to create a single cell suspensions by mechanical dissociation and digestion with collagenase at 37C. Live cells were collected by flow cytometry. 10x Chromium scRNA-seq; Single-cell suspensions were processed and single cell RNA-seq data were generated using the 10X Genomics Chromium Controller by the University of Michigan Advanced Genomics Core. Illumina NovaSeq 6000 SRX23809547 GSM8121910_r1 SRP492800 PRJNA1082635 SRS20632427 GSM8121910 GSM8121910 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Fresh full thickness human uterus samples obtained both during surgery for benign indications and from organ donors were used as tissue sources. When possible, the whole tissue sample was dissected into two anatomic segments (endometrium, myometrium). These segments separately were used to create a single cell suspensions by mechanical dissociation and digestion with collagenase at 37C. Live cells were collected by flow cytometry. 10x Chromium scRNA-seq; Single-cell suspensions were processed and single cell RNA-seq data were generated using the 10X Genomics Chromium Controller by the University of Michigan Advanced Genomics Core. Illumina NovaSeq 6000 SRX23809548 GSM8121911_r1 SRP492800 PRJNA1082635 SRS20632435 GSM8121911 GSM8121911 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Fresh full thickness human uterus samples obtained both during surgery for benign indications and from organ donors were used as tissue sources. When possible, the whole tissue sample was dissected into two anatomic segments (endometrium, myometrium). These segments separately were used to create a single cell suspensions by mechanical dissociation and digestion with collagenase at 37C. Live cells were collected by flow cytometry. 10x Chromium scRNA-seq; Single-cell suspensions were processed and single cell RNA-seq data were generated using the 10X Genomics Chromium Controller by the University of Michigan Advanced Genomics Core. Illumina NovaSeq 6000 SRX23809549 GSM8121912_r1 SRP492800 PRJNA1082635 SRS20632429 GSM8121912 GSM8121912 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Fresh full thickness human uterus samples obtained both during surgery for benign indications and from organ donors were used as tissue sources. When possible, the whole tissue sample was dissected into two anatomic segments (endometrium, myometrium). These segments separately were used to create a single cell suspensions by mechanical dissociation and digestion with collagenase at 37C. Live cells were collected by flow cytometry. 10x Chromium scRNA-seq; Single-cell suspensions were processed and single cell RNA-seq data were generated using the 10X Genomics Chromium Controller by the University of Michigan Advanced Genomics Core. Illumina NovaSeq 6000 SRX23809550 GSM8121919_r1 SRP492800 PRJNA1082635 SRS20632428 GSM8121919 GSM8121919 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Fresh full thickness human uterus samples obtained both during surgery for benign indications and from organ donors were used as tissue sources. When possible, the whole tissue sample was dissected into two anatomic segments (endometrium, myometrium). These segments separately were used to create a single cell suspensions by mechanical dissociation and digestion with collagenase at 37C. Live cells were collected by flow cytometry. 10x Chromium scRNA-seq; Single-cell suspensions were processed and single cell RNA-seq data were generated using the 10X Genomics Chromium Controller by the University of Michigan Advanced Genomics Core. Illumina NovaSeq 6000 SRX23809551 GSM8121913_r1 SRP492800 PRJNA1082635 SRS20632430 GSM8121913 GSM8121913 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Fresh full thickness human uterus samples obtained both during surgery for benign indications and from organ donors were used as tissue sources. When possible, the whole tissue sample was dissected into two anatomic segments (endometrium, myometrium). These segments separately were used to create a single cell suspensions by mechanical dissociation and digestion with collagenase at 37C. Live cells were collected by flow cytometry. 10x Chromium scRNA-seq; Single-cell suspensions were processed and single cell RNA-seq data were generated using the 10X Genomics Chromium Controller by the University of Michigan Advanced Genomics Core. Illumina NovaSeq 6000 SRX23809552 GSM8121914_r1 SRP492800 PRJNA1082635 SRS20632431 GSM8121914 GSM8121914 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Fresh full thickness human uterus samples obtained both during surgery for benign indications and from organ donors were used as tissue sources. When possible, the whole tissue sample was dissected into two anatomic segments (endometrium, myometrium). These segments separately were used to create a single cell suspensions by mechanical dissociation and digestion with collagenase at 37C. Live cells were collected by flow cytometry. 10x Chromium scRNA-seq; Single-cell suspensions were processed and single cell RNA-seq data were generated using the 10X Genomics Chromium Controller by the University of Michigan Advanced Genomics Core. Illumina NovaSeq 6000 SRX23809553 GSM8121917_r1 SRP492800 PRJNA1082635 SRS20632432 GSM8121917 GSM8121917 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Fresh full thickness human uterus samples obtained both during surgery for benign indications and from organ donors were used as tissue sources. When possible, the whole tissue sample was dissected into two anatomic segments (endometrium, myometrium). These segments separately were used to create a single cell suspensions by mechanical dissociation and digestion with collagenase at 37C. Live cells were collected by flow cytometry. 10x Chromium scRNA-seq; Single-cell suspensions were processed and single cell RNA-seq data were generated using the 10X Genomics Chromium Controller by the University of Michigan Advanced Genomics Core. Illumina NovaSeq 6000 SRX23809554 GSM8121916_r1 SRP492800 PRJNA1082635 SRS20632434 GSM8121916 GSM8121916 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Fresh full thickness human uterus samples obtained both during surgery for benign indications and from organ donors were used as tissue sources. When possible, the whole tissue sample was dissected into two anatomic segments (endometrium, myometrium). These segments separately were used to create a single cell suspensions by mechanical dissociation and digestion with collagenase at 37C. Live cells were collected by flow cytometry. 10x Chromium scRNA-seq; Single-cell suspensions were processed and single cell RNA-seq data were generated using the 10X Genomics Chromium Controller by the University of Michigan Advanced Genomics Core. Illumina NovaSeq 6000 SRX23809555 GSM8121915_r1 SRP492800 PRJNA1082635 SRS20632433 GSM8121915 GSM8121915 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Fresh full thickness human uterus samples obtained both during surgery for benign indications and from organ donors were used as tissue sources. When possible, the whole tissue sample was dissected into two anatomic segments (endometrium, myometrium). These segments separately were used to create a single cell suspensions by mechanical dissociation and digestion with collagenase at 37C. Live cells were collected by flow cytometry. 10x Chromium scRNA-seq; Single-cell suspensions were processed and single cell RNA-seq data were generated using the 10X Genomics Chromium Controller by the University of Michigan Advanced Genomics Core. Illumina NovaSeq 6000 SRX23809556 GSM8121918_r1 SRP492800 PRJNA1082635 SRS20632436 GSM8121918 GSM8121918 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Fresh full thickness human uterus samples obtained both during surgery for benign indications and from organ donors were used as tissue sources. When possible, the whole tissue sample was dissected into two anatomic segments (endometrium, myometrium). These segments separately were used to create a single cell suspensions by mechanical dissociation and digestion with collagenase at 37C. Live cells were collected by flow cytometry. 10x Chromium scRNA-seq; Single-cell suspensions were processed and single cell RNA-seq data were generated using the 10X Genomics Chromium Controller by the University of Michigan Advanced Genomics Core. Illumina NovaSeq 6000