SRX4409681 GSM3293966 SRP154483 SRS3563315 GSM3293966 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293966 GSM3293966 GEO Accession GSM3293966 SRX4409682 GSM3293967 SRP154483 SRS3563316 GSM3293967 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293967 GSM3293967 GEO Accession GSM3293967 SRX4409683 GSM3293968 SRP154483 SRS3563317 GSM3293968 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293968 GSM3293968 GEO Accession GSM3293968 SRX4409684 GSM3293969 SRP154483 SRS3563318 GSM3293969 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293969 GSM3293969 GEO Accession GSM3293969 SRX4409685 GSM3293970 SRP154483 SRS3563380 GSM3293970 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293970 GSM3293970 GEO Accession GSM3293970 SRX4409686 GSM3293971 SRP154483 SRS3563319 GSM3293971 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293971 GSM3293971 GEO Accession GSM3293971 SRX4409687 GSM3293972 SRP154483 SRS3563320 GSM3293972 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293972 GSM3293972 GEO Accession GSM3293972 SRX4409688 GSM3293973 SRP154483 SRS3563321 GSM3293973 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293973 GSM3293973 GEO Accession GSM3293973 SRX4409689 GSM3293974 SRP154483 SRS3563322 GSM3293974 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293974 GSM3293974 GEO Accession GSM3293974 SRX4409690 GSM3293975 SRP154483 SRS3563323 GSM3293975 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293975 GSM3293975 GEO Accession GSM3293975 SRX4409691 GSM3293976 SRP154483 SRS3563324 GSM3293976 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293976 GSM3293976 GEO Accession GSM3293976 SRX4409692 GSM3293977 SRP154483 SRS3563325 GSM3293977 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293977 GSM3293977 GEO Accession GSM3293977 SRX4409693 GSM3293978 SRP154483 SRS3563327 GSM3293978 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293978 GSM3293978 GEO Accession GSM3293978 SRX4409694 GSM3293979 SRP154483 SRS3563328 GSM3293979 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293979 GSM3293979 GEO Accession GSM3293979 SRX4409695 GSM3293980 SRP154483 SRS3563326 GSM3293980 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293980 GSM3293980 GEO Accession GSM3293980 SRX4409696 GSM3293981 SRP154483 SRS3563329 GSM3293981 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293981 GSM3293981 GEO Accession GSM3293981 SRX4409697 GSM3293982 SRP154483 SRS3563331 GSM3293982 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293982 GSM3293982 GEO Accession GSM3293982 SRX4409698 GSM3293983 SRP154483 SRS3563330 GSM3293983 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293983 GSM3293983 GEO Accession GSM3293983 SRX4409699 GSM3293984 SRP154483 SRS3563332 GSM3293984 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293984 GSM3293984 GEO Accession GSM3293984 SRX4409700 GSM3293985 SRP154483 SRS3563334 GSM3293985 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293985 GSM3293985 GEO Accession GSM3293985 SRX4409701 GSM3293986 SRP154483 SRS3563333 GSM3293986 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293986 GSM3293986 GEO Accession GSM3293986 SRX4409702 GSM3293987 SRP154483 SRS3563335 GSM3293987 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293987 GSM3293987 GEO Accession GSM3293987 SRX4409703 GSM3293988 SRP154483 SRS3563336 GSM3293988 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293988 GSM3293988 GEO Accession GSM3293988 SRX4409704 GSM3293989 SRP154483 SRS3563337 GSM3293989 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293989 GSM3293989 GEO Accession GSM3293989 SRX4409705 GSM3293990 SRP154483 SRS3563338 GSM3293990 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293990 GSM3293990 GEO Accession GSM3293990 SRX4409706 GSM3293991 SRP154483 SRS3563339 GSM3293991 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293991 GSM3293991 GEO Accession GSM3293991 SRX4409707 GSM3293992 SRP154483 SRS3563340 GSM3293992 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293992 GSM3293992 GEO Accession GSM3293992 SRX4409708 GSM3293993 SRP154483 SRS3563341 GSM3293993 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293993 GSM3293993 GEO Accession GSM3293993 SRX4409709 GSM3293994 SRP154483 SRS3563343 GSM3293994 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293994 GSM3293994 GEO Accession GSM3293994 SRX4409710 GSM3293995 SRP154483 SRS3563342 GSM3293995 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293995 GSM3293995 GEO Accession GSM3293995 SRX4409711 GSM3293996 SRP154483 SRS3563345 GSM3293996 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293996 GSM3293996 GEO Accession GSM3293996 SRX4409712 GSM3293997 SRP154483 SRS3563344 GSM3293997 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293997 GSM3293997 GEO Accession GSM3293997 SRX4409713 GSM3293998 SRP154483 SRS3563346 GSM3293998 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293998 GSM3293998 GEO Accession GSM3293998 SRX4409714 GSM3293999 SRP154483 SRS3563347 GSM3293999 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303293999 GSM3293999 GEO Accession GSM3293999 SRX4409715 GSM3294000 SRP154483 SRS3563348 GSM3294000 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294000 GSM3294000 GEO Accession GSM3294000 SRX4409716 GSM3294001 SRP154483 SRS3563349 GSM3294001 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294001 GSM3294001 GEO Accession GSM3294001 SRX4409717 GSM3294002 SRP154483 SRS3563350 GSM3294002 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294002 GSM3294002 GEO Accession GSM3294002 SRX4409718 GSM3294003 SRP154483 SRS3563351 GSM3294003 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294003 GSM3294003 GEO Accession GSM3294003 SRX4409719 GSM3294004 SRP154483 SRS3563352 GSM3294004 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294004 GSM3294004 GEO Accession GSM3294004 SRX4409720 GSM3294005 SRP154483 SRS3563353 GSM3294005 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294005 GSM3294005 GEO Accession GSM3294005 SRX4409721 GSM3294006 SRP154483 SRS3563354 GSM3294006 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294006 GSM3294006 GEO Accession GSM3294006 SRX4409722 GSM3294007 SRP154483 SRS3563355 GSM3294007 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294007 GSM3294007 GEO Accession GSM3294007 SRX4409723 GSM3294008 SRP154483 SRS3563356 GSM3294008 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294008 GSM3294008 GEO Accession GSM3294008 SRX4409724 GSM3294009 SRP154483 SRS3563357 GSM3294009 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294009 GSM3294009 GEO Accession GSM3294009 SRX4409725 GSM3294010 SRP154483 SRS3563358 GSM3294010 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294010 GSM3294010 GEO Accession GSM3294010 SRX4409726 GSM3294011 SRP154483 SRS3563359 GSM3294011 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294011 GSM3294011 GEO Accession GSM3294011 SRX4409727 GSM3294012 SRP154483 SRS3563360 GSM3294012 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294012 GSM3294012 GEO Accession GSM3294012 SRX4409728 GSM3294013 SRP154483 SRS3563361 GSM3294013 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294013 GSM3294013 GEO Accession GSM3294013 SRX4409729 GSM3294014 SRP154483 SRS3563362 GSM3294014 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294014 GSM3294014 GEO Accession GSM3294014 SRX4409730 GSM3294015 SRP154483 SRS3563363 GSM3294015 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294015 GSM3294015 GEO Accession GSM3294015 SRX4409731 GSM3294016 SRP154483 SRS3563364 GSM3294016 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294016 GSM3294016 GEO Accession GSM3294016 SRX4409732 GSM3294017 SRP154483 SRS3563365 GSM3294017 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294017 GSM3294017 GEO Accession GSM3294017 SRX4409733 GSM3294018 SRP154483 SRS3563366 GSM3294018 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294018 GSM3294018 GEO Accession GSM3294018 SRX4409734 GSM3294019 SRP154483 SRS3563367 GSM3294019 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294019 GSM3294019 GEO Accession GSM3294019 SRX4409735 GSM3294020 SRP154483 SRS3563368 GSM3294020 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294020 GSM3294020 GEO Accession GSM3294020 SRX4409736 GSM3294021 SRP154483 SRS3563369 GSM3294021 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294021 GSM3294021 GEO Accession GSM3294021 SRX4409737 GSM3294022 SRP154483 SRS3563370 GSM3294022 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294022 GSM3294022 GEO Accession GSM3294022 SRX4409738 GSM3294023 SRP154483 SRS3563372 GSM3294023 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294023 GSM3294023 GEO Accession GSM3294023 SRX4409739 GSM3294024 SRP154483 SRS3563371 GSM3294024 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294024 GSM3294024 GEO Accession GSM3294024 SRX4409740 GSM3294025 SRP154483 SRS3563373 GSM3294025 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294025 GSM3294025 GEO Accession GSM3294025 SRX4409741 GSM3294026 SRP154483 SRS3563374 GSM3294026 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294026 GSM3294026 GEO Accession GSM3294026 SRX4409742 GSM3294027 SRP154483 SRS3563375 GSM3294027 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294027 GSM3294027 GEO Accession GSM3294027 SRX4409743 GSM3294028 SRP154483 SRS3563377 GSM3294028 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294028 GSM3294028 GEO Accession GSM3294028 SRX4409744 GSM3294029 SRP154483 SRS3563376 GSM3294029 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294029 GSM3294029 GEO Accession GSM3294029 SRX4409745 GSM3294030 SRP154483 SRS3563378 GSM3294030 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294030 GSM3294030 GEO Accession GSM3294030 SRX4409746 GSM3294031 SRP154483 SRS3563379 GSM3294031 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294031 GSM3294031 GEO Accession GSM3294031 SRX4409747 GSM3294032 SRP154483 SRS3563381 GSM3294032 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294032 GSM3294032 GEO Accession GSM3294032 SRX4409748 GSM3294033 SRP154483 SRS3563382 GSM3294033 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294033 GSM3294033 GEO Accession GSM3294033 SRX4409749 GSM3294034 SRP154483 SRS3563383 GSM3294034 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294034 GSM3294034 GEO Accession GSM3294034 SRX4409750 GSM3294035 SRP154483 SRS3563384 GSM3294035 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294035 GSM3294035 GEO Accession GSM3294035 SRX4409751 GSM3294036 SRP154483 SRS3563385 GSM3294036 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294036 GSM3294036 GEO Accession GSM3294036 SRX4409752 GSM3294037 SRP154483 SRS3563386 GSM3294037 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294037 GSM3294037 GEO Accession GSM3294037 SRX4409753 GSM3294038 SRP154483 SRS3563388 GSM3294038 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294038 GSM3294038 GEO Accession GSM3294038 SRX4409754 GSM3294039 SRP154483 SRS3563389 GSM3294039 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294039 GSM3294039 GEO Accession GSM3294039 SRX4409755 GSM3294040 SRP154483 SRS3563387 GSM3294040 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294040 GSM3294040 GEO Accession GSM3294040 SRX4409756 GSM3294041 SRP154483 SRS3563390 GSM3294041 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294041 GSM3294041 GEO Accession GSM3294041 SRX4409757 GSM3294042 SRP154483 SRS3563392 GSM3294042 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294042 GSM3294042 GEO Accession GSM3294042 SRX4409758 GSM3294043 SRP154483 SRS3563391 GSM3294043 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294043 GSM3294043 GEO Accession GSM3294043 SRX4409759 GSM3294044 SRP154483 SRS3563393 GSM3294044 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294044 GSM3294044 GEO Accession GSM3294044 SRX4409760 GSM3294045 SRP154483 SRS3563394 GSM3294045 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294045 GSM3294045 GEO Accession GSM3294045 SRX4409761 GSM3294046 SRP154483 SRS3563395 GSM3294046 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294046 GSM3294046 GEO Accession GSM3294046 SRX4409762 GSM3294047 SRP154483 SRS3563396 GSM3294047 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294047 GSM3294047 GEO Accession GSM3294047 SRX4409763 GSM3294048 SRP154483 SRS3563397 GSM3294048 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294048 GSM3294048 GEO Accession GSM3294048 SRX4409764 GSM3294049 SRP154483 SRS3563398 GSM3294049 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294049 GSM3294049 GEO Accession GSM3294049 SRX4409765 GSM3294050 SRP154483 SRS3563399 GSM3294050 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294050 GSM3294050 GEO Accession GSM3294050 SRX4409766 GSM3294051 SRP154483 SRS3563400 GSM3294051 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294051 GSM3294051 GEO Accession GSM3294051 SRX4409767 GSM3294052 SRP154483 SRS3563401 GSM3294052 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294052 GSM3294052 GEO Accession GSM3294052 SRX4409768 GSM3294053 SRP154483 SRS3563402 GSM3294053 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294053 GSM3294053 GEO Accession GSM3294053 SRX4409769 GSM3294054 SRP154483 SRS3563403 GSM3294054 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294054 GSM3294054 GEO Accession GSM3294054 SRX4409770 GSM3294055 SRP154483 SRS3563404 GSM3294055 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294055 GSM3294055 GEO Accession GSM3294055 SRX4409771 GSM3294056 SRP154483 SRS3563405 GSM3294056 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294056 GSM3294056 GEO Accession GSM3294056 SRX4409772 GSM3294057 SRP154483 SRS3563407 GSM3294057 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294057 GSM3294057 GEO Accession GSM3294057 SRX4409773 GSM3294058 SRP154483 SRS3563406 GSM3294058 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294058 GSM3294058 GEO Accession GSM3294058 SRX4409774 GSM3294059 SRP154483 SRS3563408 GSM3294059 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294059 GSM3294059 GEO Accession GSM3294059 SRX4409775 GSM3294060 SRP154483 SRS3563409 GSM3294060 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294060 GSM3294060 GEO Accession GSM3294060 SRX4409776 GSM3294061 SRP154483 SRS3563410 GSM3294061 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294061 GSM3294061 GEO Accession GSM3294061 SRX4409777 GSM3294062 SRP154483 SRS3563411 GSM3294062 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294062 GSM3294062 GEO Accession GSM3294062 SRX4409778 GSM3294063 SRP154483 SRS3563412 GSM3294063 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294063 GSM3294063 GEO Accession GSM3294063 SRX4409779 GSM3294064 SRP154483 SRS3563413 GSM3294064 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294064 GSM3294064 GEO Accession GSM3294064 SRX4409780 GSM3294065 SRP154483 SRS3563414 GSM3294065 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294065 GSM3294065 GEO Accession GSM3294065 SRX4409781 GSM3294066 SRP154483 SRS3563415 GSM3294066 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294066 GSM3294066 GEO Accession GSM3294066 SRX4409782 GSM3294067 SRP154483 SRS3563416 GSM3294067 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294067 GSM3294067 GEO Accession GSM3294067 SRX4409783 GSM3294068 SRP154483 SRS3563417 GSM3294068 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294068 GSM3294068 GEO Accession GSM3294068 SRX4409784 GSM3294069 SRP154483 SRS3563418 GSM3294069 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294069 GSM3294069 GEO Accession GSM3294069 SRX4409785 GSM3294070 SRP154483 SRS3563419 GSM3294070 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294070 GSM3294070 GEO Accession GSM3294070 SRX4409786 GSM3294071 SRP154483 SRS3563420 GSM3294071 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294071 GSM3294071 GEO Accession GSM3294071 SRX4409787 GSM3294072 SRP154483 SRS3563422 GSM3294072 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294072 GSM3294072 GEO Accession GSM3294072 SRX4409788 GSM3294073 SRP154483 SRS3563423 GSM3294073 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294073 GSM3294073 GEO Accession GSM3294073 SRX4409789 GSM3294074 SRP154483 SRS3563421 GSM3294074 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294074 GSM3294074 GEO Accession GSM3294074 SRX4409790 GSM3294075 SRP154483 SRS3563424 GSM3294075 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294075 GSM3294075 GEO Accession GSM3294075 SRX4409791 GSM3294076 SRP154483 SRS3563425 GSM3294076 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294076 GSM3294076 GEO Accession GSM3294076 SRX4409792 GSM3294077 SRP154483 SRS3563427 GSM3294077 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294077 GSM3294077 GEO Accession GSM3294077 SRX4409793 GSM3294078 SRP154483 SRS3563426 GSM3294078 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294078 GSM3294078 GEO Accession GSM3294078 SRX4409794 GSM3294079 SRP154483 SRS3563428 GSM3294079 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294079 GSM3294079 GEO Accession GSM3294079 SRX4409795 GSM3294080 SRP154483 SRS3563429 GSM3294080 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294080 GSM3294080 GEO Accession GSM3294080 SRX4409796 GSM3294081 SRP154483 SRS3563430 GSM3294081 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294081 GSM3294081 GEO Accession GSM3294081 SRX4409797 GSM3294082 SRP154483 SRS3563431 GSM3294082 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294082 GSM3294082 GEO Accession GSM3294082 SRX4409798 GSM3294083 SRP154483 SRS3563432 GSM3294083 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294083 GSM3294083 GEO Accession GSM3294083 SRX4409799 GSM3294084 SRP154483 SRS3563433 GSM3294084 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294084 GSM3294084 GEO Accession GSM3294084 SRX4409800 GSM3294085 SRP154483 SRS3563434 GSM3294085 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294085 GSM3294085 GEO Accession GSM3294085 SRX4409801 GSM3294086 SRP154483 SRS3563435 GSM3294086 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294086 GSM3294086 GEO Accession GSM3294086 SRX4409802 GSM3294087 SRP154483 SRS3563436 GSM3294087 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294087 GSM3294087 GEO Accession GSM3294087 SRX4409803 GSM3294088 SRP154483 SRS3563437 GSM3294088 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294088 GSM3294088 GEO Accession GSM3294088 SRX4409804 GSM3294089 SRP154483 SRS3563438 GSM3294089 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294089 GSM3294089 GEO Accession GSM3294089 SRX4409805 GSM3294090 SRP154483 SRS3563439 GSM3294090 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294090 GSM3294090 GEO Accession GSM3294090 SRX4409806 GSM3294091 SRP154483 SRS3563440 GSM3294091 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294091 GSM3294091 GEO Accession GSM3294091 SRX4409807 GSM3294092 SRP154483 SRS3563441 GSM3294092 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294092 GSM3294092 GEO Accession GSM3294092 SRX4409808 GSM3294093 SRP154483 SRS3563442 GSM3294093 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294093 GSM3294093 GEO Accession GSM3294093 SRX4409809 GSM3294094 SRP154483 SRS3563443 GSM3294094 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294094 GSM3294094 GEO Accession GSM3294094 SRX4409810 GSM3294095 SRP154483 SRS3563444 GSM3294095 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294095 GSM3294095 GEO Accession GSM3294095 SRX4409811 GSM3294096 SRP154483 SRS3563445 GSM3294096 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294096 GSM3294096 GEO Accession GSM3294096 SRX4409812 GSM3294097 SRP154483 SRS3563446 GSM3294097 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294097 GSM3294097 GEO Accession GSM3294097 SRX4409813 GSM3294098 SRP154483 SRS3563447 GSM3294098 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294098 GSM3294098 GEO Accession GSM3294098 SRX4409814 GSM3294099 SRP154483 SRS3563449 GSM3294099 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294099 GSM3294099 GEO Accession GSM3294099 SRX4409815 GSM3294100 SRP154483 SRS3563450 GSM3294100 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294100 GSM3294100 GEO Accession GSM3294100 SRX4409816 GSM3294101 SRP154483 SRS3563448 GSM3294101 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294101 GSM3294101 GEO Accession GSM3294101 SRX4409817 GSM3294102 SRP154483 SRS3563452 GSM3294102 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294102 GSM3294102 GEO Accession GSM3294102 SRX4409818 GSM3294103 SRP154483 SRS3563451 GSM3294103 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294103 GSM3294103 GEO Accession GSM3294103 SRX4409819 GSM3294104 SRP154483 SRS3563454 GSM3294104 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294104 GSM3294104 GEO Accession GSM3294104 SRX4409820 GSM3294105 SRP154483 SRS3563453 GSM3294105 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294105 GSM3294105 GEO Accession GSM3294105 SRX4409821 GSM3294106 SRP154483 SRS3563456 GSM3294106 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294106 GSM3294106 GEO Accession GSM3294106 SRX4409822 GSM3294107 SRP154483 SRS3563455 GSM3294107 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294107 GSM3294107 GEO Accession GSM3294107 SRX4409823 GSM3294108 SRP154483 SRS3563457 GSM3294108 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294108 GSM3294108 GEO Accession GSM3294108 SRX4409824 GSM3294109 SRP154483 SRS3563458 GSM3294109 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294109 GSM3294109 GEO Accession GSM3294109 SRX4409825 GSM3294110 SRP154483 SRS3563459 GSM3294110 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294110 GSM3294110 GEO Accession GSM3294110 SRX4409826 GSM3294111 SRP154483 SRS3563460 GSM3294111 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294111 GSM3294111 GEO Accession GSM3294111 SRX4409827 GSM3294112 SRP154483 SRS3563461 GSM3294112 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294112 GSM3294112 GEO Accession GSM3294112 SRX4409828 GSM3294113 SRP154483 SRS3563462 GSM3294113 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294113 GSM3294113 GEO Accession GSM3294113 SRX4409829 GSM3294114 SRP154483 SRS3563464 GSM3294114 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294114 GSM3294114 GEO Accession GSM3294114 SRX4409830 GSM3294115 SRP154483 SRS3563463 GSM3294115 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294115 GSM3294115 GEO Accession GSM3294115 SRX4409831 GSM3294116 SRP154483 SRS3563465 GSM3294116 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294116 GSM3294116 GEO Accession GSM3294116 SRX4409832 GSM3294117 SRP154483 SRS3563466 GSM3294117 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294117 GSM3294117 GEO Accession GSM3294117 SRX4409833 GSM3294118 SRP154483 SRS3563467 GSM3294118 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294118 GSM3294118 GEO Accession GSM3294118 SRX4409834 GSM3294119 SRP154483 SRS3563468 GSM3294119 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294119 GSM3294119 GEO Accession GSM3294119 SRX4409835 GSM3294120 SRP154483 SRS3563469 GSM3294120 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294120 GSM3294120 GEO Accession GSM3294120 SRX4409836 GSM3294121 SRP154483 SRS3563470 GSM3294121 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294121 GSM3294121 GEO Accession GSM3294121 SRX4409837 GSM3294122 SRP154483 SRS3563471 GSM3294122 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294122 GSM3294122 GEO Accession GSM3294122 SRX4409838 GSM3294123 SRP154483 SRS3563472 GSM3294123 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294123 GSM3294123 GEO Accession GSM3294123 SRX4409839 GSM3294124 SRP154483 SRS3563473 GSM3294124 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294124 GSM3294124 GEO Accession GSM3294124 SRX4409840 GSM3294125 SRP154483 SRS3563477 GSM3294125 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294125 GSM3294125 GEO Accession GSM3294125 SRX4409841 GSM3294126 SRP154483 SRS3563474 GSM3294126 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294126 GSM3294126 GEO Accession GSM3294126 SRX4409842 GSM3294127 SRP154483 SRS3563476 GSM3294127 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294127 GSM3294127 GEO Accession GSM3294127 SRX4409843 GSM3294128 SRP154483 SRS3563475 GSM3294128 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294128 GSM3294128 GEO Accession GSM3294128 SRX4409844 GSM3294129 SRP154483 SRS3563479 GSM3294129 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294129 GSM3294129 GEO Accession GSM3294129 SRX4409845 GSM3294130 SRP154483 SRS3563478 GSM3294130 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294130 GSM3294130 GEO Accession GSM3294130 SRX4409846 GSM3294131 SRP154483 SRS3563480 GSM3294131 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294131 GSM3294131 GEO Accession GSM3294131 SRX4409847 GSM3294132 SRP154483 SRS3563482 GSM3294132 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294132 GSM3294132 GEO Accession GSM3294132 SRX4409848 GSM3294133 SRP154483 SRS3563481 GSM3294133 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294133 GSM3294133 GEO Accession GSM3294133 SRX4409849 GSM3294134 SRP154483 SRS3563483 GSM3294134 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294134 GSM3294134 GEO Accession GSM3294134 SRX4409850 GSM3294135 SRP154483 SRS3563484 GSM3294135 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294135 GSM3294135 GEO Accession GSM3294135 SRX4409851 GSM3294136 SRP154483 SRS3563486 GSM3294136 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294136 GSM3294136 GEO Accession GSM3294136 SRX4409852 GSM3294137 SRP154483 SRS3563485 GSM3294137 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294137 GSM3294137 GEO Accession GSM3294137 SRX4409853 GSM3294138 SRP154483 SRS3563487 GSM3294138 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294138 GSM3294138 GEO Accession GSM3294138 SRX4409854 GSM3294139 SRP154483 SRS3563489 GSM3294139 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294139 GSM3294139 GEO Accession GSM3294139 SRX4409855 GSM3294140 SRP154483 SRS3563488 GSM3294140 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294140 GSM3294140 GEO Accession GSM3294140 SRX4409856 GSM3294141 SRP154483 SRS3563490 GSM3294141 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294141 GSM3294141 GEO Accession GSM3294141 SRX4409857 GSM3294142 SRP154483 SRS3563491 GSM3294142 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294142 GSM3294142 GEO Accession GSM3294142 SRX4409858 GSM3294143 SRP154483 SRS3563492 GSM3294143 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294143 GSM3294143 GEO Accession GSM3294143 SRX4409859 GSM3294144 SRP154483 SRS3563493 GSM3294144 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294144 GSM3294144 GEO Accession GSM3294144 SRX4409860 GSM3294145 SRP154483 SRS3563631 GSM3294145 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294145 GSM3294145 GEO Accession GSM3294145 SRX4409861 GSM3294146 SRP154483 SRS3563494 GSM3294146 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294146 GSM3294146 GEO Accession GSM3294146 SRX4409862 GSM3294147 SRP154483 SRS3563495 GSM3294147 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294147 GSM3294147 GEO Accession GSM3294147 SRX4409863 GSM3294148 SRP154483 SRS3563496 GSM3294148 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294148 GSM3294148 GEO Accession GSM3294148 SRX4409864 GSM3294149 SRP154483 SRS3563497 GSM3294149 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294149 GSM3294149 GEO Accession GSM3294149 SRX4409865 GSM3294150 SRP154483 SRS3563498 GSM3294150 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294150 GSM3294150 GEO Accession GSM3294150 SRX4409866 GSM3294151 SRP154483 SRS3563499 GSM3294151 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294151 GSM3294151 GEO Accession GSM3294151 SRX4409867 GSM3294152 SRP154483 SRS3563500 GSM3294152 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294152 GSM3294152 GEO Accession GSM3294152 SRX4409868 GSM3294153 SRP154483 SRS3563502 GSM3294153 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294153 GSM3294153 GEO Accession GSM3294153 SRX4409869 GSM3294154 SRP154483 SRS3563501 GSM3294154 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294154 GSM3294154 GEO Accession GSM3294154 SRX4409870 GSM3294155 SRP154483 SRS3563503 GSM3294155 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294155 GSM3294155 GEO Accession GSM3294155 SRX4409871 GSM3294156 SRP154483 SRS3563504 GSM3294156 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294156 GSM3294156 GEO Accession GSM3294156 SRX4409872 GSM3294157 SRP154483 SRS3563505 GSM3294157 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294157 GSM3294157 GEO Accession GSM3294157 SRX4409873 GSM3294158 SRP154483 SRS3563506 GSM3294158 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294158 GSM3294158 GEO Accession GSM3294158 SRX4409874 GSM3294159 SRP154483 SRS3563507 GSM3294159 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294159 GSM3294159 GEO Accession GSM3294159 SRX4409875 GSM3294160 SRP154483 SRS3563508 GSM3294160 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294160 GSM3294160 GEO Accession GSM3294160 SRX4409876 GSM3294161 SRP154483 SRS3563509 GSM3294161 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294161 GSM3294161 GEO Accession GSM3294161 SRX4409877 GSM3294162 SRP154483 SRS3563510 GSM3294162 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294162 GSM3294162 GEO Accession GSM3294162 SRX4409878 GSM3294163 SRP154483 SRS3563511 GSM3294163 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294163 GSM3294163 GEO Accession GSM3294163 SRX4409879 GSM3294164 SRP154483 SRS3563512 GSM3294164 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294164 GSM3294164 GEO Accession GSM3294164 SRX4409880 GSM3294165 SRP154483 SRS3563513 GSM3294165 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294165 GSM3294165 GEO Accession GSM3294165 SRX4409881 GSM3294166 SRP154483 SRS3563514 GSM3294166 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294166 GSM3294166 GEO Accession GSM3294166 SRX4409882 GSM3294167 SRP154483 SRS3563515 GSM3294167 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294167 GSM3294167 GEO Accession GSM3294167 SRX4409883 GSM3294168 SRP154483 SRS3563516 GSM3294168 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294168 GSM3294168 GEO Accession GSM3294168 SRX4409884 GSM3294169 SRP154483 SRS3563517 GSM3294169 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294169 GSM3294169 GEO Accession GSM3294169 SRX4409885 GSM3294170 SRP154483 SRS3563518 GSM3294170 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294170 GSM3294170 GEO Accession GSM3294170 SRX4409886 GSM3294171 SRP154483 SRS3563519 GSM3294171 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294171 GSM3294171 GEO Accession GSM3294171 SRX4409887 GSM3294172 SRP154483 SRS3563520 GSM3294172 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294172 GSM3294172 GEO Accession GSM3294172 SRX4409888 GSM3294173 SRP154483 SRS3563521 GSM3294173 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294173 GSM3294173 GEO Accession GSM3294173 SRX4409889 GSM3294174 SRP154483 SRS3563523 GSM3294174 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294174 GSM3294174 GEO Accession GSM3294174 SRX4409890 GSM3294175 SRP154483 SRS3563522 GSM3294175 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294175 GSM3294175 GEO Accession GSM3294175 SRX4409891 GSM3294176 SRP154483 SRS3563524 GSM3294176 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294176 GSM3294176 GEO Accession GSM3294176 SRX4409892 GSM3294177 SRP154483 SRS3563525 GSM3294177 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294177 GSM3294177 GEO Accession GSM3294177 SRX4409893 GSM3294178 SRP154483 SRS3563526 GSM3294178 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294178 GSM3294178 GEO Accession GSM3294178 SRX4409894 GSM3294179 SRP154483 SRS3563528 GSM3294179 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294179 GSM3294179 GEO Accession GSM3294179 SRX4409895 GSM3294180 SRP154483 SRS3563530 GSM3294180 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294180 GSM3294180 GEO Accession GSM3294180 SRX4409896 GSM3294181 SRP154483 SRS3563527 GSM3294181 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294181 GSM3294181 GEO Accession GSM3294181 SRX4409897 GSM3294182 SRP154483 SRS3563532 GSM3294182 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294182 GSM3294182 GEO Accession GSM3294182 SRX4409898 GSM3294183 SRP154483 SRS3563529 GSM3294183 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294183 GSM3294183 GEO Accession GSM3294183 SRX4409899 GSM3294184 SRP154483 SRS3563531 GSM3294184 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294184 GSM3294184 GEO Accession GSM3294184 SRX4409900 GSM3294185 SRP154483 SRS3563533 GSM3294185 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294185 GSM3294185 GEO Accession GSM3294185 SRX4409901 GSM3294186 SRP154483 SRS3563536 GSM3294186 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294186 GSM3294186 GEO Accession GSM3294186 SRX4409902 GSM3294187 SRP154483 SRS3563534 GSM3294187 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294187 GSM3294187 GEO Accession GSM3294187 SRX4409903 GSM3294188 SRP154483 SRS3563535 GSM3294188 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294188 GSM3294188 GEO Accession GSM3294188 SRX4409904 GSM3294189 SRP154483 SRS3563537 GSM3294189 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294189 GSM3294189 GEO Accession GSM3294189 SRX4409905 GSM3294190 SRP154483 SRS3563538 GSM3294190 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294190 GSM3294190 GEO Accession GSM3294190 SRX4409906 GSM3294191 SRP154483 SRS3563539 GSM3294191 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294191 GSM3294191 GEO Accession GSM3294191 SRX4409907 GSM3294192 SRP154483 SRS3563540 GSM3294192 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294192 GSM3294192 GEO Accession GSM3294192 SRX4409908 GSM3294193 SRP154483 SRS3563541 GSM3294193 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294193 GSM3294193 GEO Accession GSM3294193 SRX4409909 GSM3294194 SRP154483 SRS3563542 GSM3294194 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294194 GSM3294194 GEO Accession GSM3294194 SRX4409910 GSM3294195 SRP154483 SRS3563544 GSM3294195 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294195 GSM3294195 GEO Accession GSM3294195 SRX4409911 GSM3294196 SRP154483 SRS3563545 GSM3294196 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294196 GSM3294196 GEO Accession GSM3294196 SRX4409912 GSM3294197 SRP154483 SRS3563543 GSM3294197 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294197 GSM3294197 GEO Accession GSM3294197 SRX4409913 GSM3294198 SRP154483 SRS3563546 GSM3294198 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294198 GSM3294198 GEO Accession GSM3294198 SRX4409914 GSM3294199 SRP154483 SRS3563548 GSM3294199 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294199 GSM3294199 GEO Accession GSM3294199 SRX4409915 GSM3294200 SRP154483 SRS3563547 GSM3294200 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294200 GSM3294200 GEO Accession GSM3294200 SRX4409916 GSM3294201 SRP154483 SRS3563549 GSM3294201 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294201 GSM3294201 GEO Accession GSM3294201 SRX4409917 GSM3294202 SRP154483 SRS3563550 GSM3294202 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294202 GSM3294202 GEO Accession GSM3294202 SRX4409918 GSM3294203 SRP154483 SRS3563552 GSM3294203 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294203 GSM3294203 GEO Accession GSM3294203 SRX4409919 GSM3294204 SRP154483 SRS3563551 GSM3294204 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294204 GSM3294204 GEO Accession GSM3294204 SRX4409920 GSM3294205 SRP154483 SRS3563554 GSM3294205 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294205 GSM3294205 GEO Accession GSM3294205 SRX4409921 GSM3294206 SRP154483 SRS3563553 GSM3294206 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294206 GSM3294206 GEO Accession GSM3294206 SRX4409922 GSM3294207 SRP154483 SRS3563555 GSM3294207 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294207 GSM3294207 GEO Accession GSM3294207 SRX4409923 GSM3294208 SRP154483 SRS3563556 GSM3294208 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294208 GSM3294208 GEO Accession GSM3294208 SRX4409924 GSM3294209 SRP154483 SRS3563558 GSM3294209 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294209 GSM3294209 GEO Accession GSM3294209 SRX4409925 GSM3294210 SRP154483 SRS3563557 GSM3294210 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294210 GSM3294210 GEO Accession GSM3294210 SRX4409926 GSM3294211 SRP154483 SRS3563559 GSM3294211 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294211 GSM3294211 GEO Accession GSM3294211 SRX4409927 GSM3294212 SRP154483 SRS3563560 GSM3294212 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294212 GSM3294212 GEO Accession GSM3294212 SRX4409928 GSM3294213 SRP154483 SRS3563562 GSM3294213 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294213 GSM3294213 GEO Accession GSM3294213 SRX4409929 GSM3294214 SRP154483 SRS3563561 GSM3294214 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294214 GSM3294214 GEO Accession GSM3294214 SRX4409930 GSM3294215 SRP154483 SRS3563563 GSM3294215 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294215 GSM3294215 GEO Accession GSM3294215 SRX4409931 GSM3294216 SRP154483 SRS3563565 GSM3294216 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294216 GSM3294216 GEO Accession GSM3294216 SRX4409932 GSM3294217 SRP154483 SRS3563564 GSM3294217 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294217 GSM3294217 GEO Accession GSM3294217 SRX4409933 GSM3294218 SRP154483 SRS3563566 GSM3294218 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294218 GSM3294218 GEO Accession GSM3294218 SRX4409934 GSM3294219 SRP154483 SRS3563567 GSM3294219 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294219 GSM3294219 GEO Accession GSM3294219 SRX4409935 GSM3294220 SRP154483 SRS3563568 GSM3294220 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294220 GSM3294220 GEO Accession GSM3294220 SRX4409936 GSM3294221 SRP154483 SRS3563569 GSM3294221 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294221 GSM3294221 GEO Accession GSM3294221 SRX4409937 GSM3294222 SRP154483 SRS3563570 GSM3294222 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294222 GSM3294222 GEO Accession GSM3294222 SRX4409938 GSM3294223 SRP154483 SRS3563571 GSM3294223 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294223 GSM3294223 GEO Accession GSM3294223 SRX4409939 GSM3294224 SRP154483 SRS3563573 GSM3294224 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294224 GSM3294224 GEO Accession GSM3294224 SRX4409940 GSM3294225 SRP154483 SRS3563572 GSM3294225 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294225 GSM3294225 GEO Accession GSM3294225 SRX4409941 GSM3294226 SRP154483 SRS3563577 GSM3294226 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294226 GSM3294226 GEO Accession GSM3294226 SRX4409942 GSM3294227 SRP154483 SRS3563574 GSM3294227 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294227 GSM3294227 GEO Accession GSM3294227 SRX4409943 GSM3294228 SRP154483 SRS3563575 GSM3294228 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294228 GSM3294228 GEO Accession GSM3294228 SRX4409944 GSM3294229 SRP154483 SRS3563576 GSM3294229 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294229 GSM3294229 GEO Accession GSM3294229 SRX4409945 GSM3294230 SRP154483 SRS3563578 GSM3294230 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294230 GSM3294230 GEO Accession GSM3294230 SRX4409946 GSM3294231 SRP154483 SRS3563579 GSM3294231 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294231 GSM3294231 GEO Accession GSM3294231 SRX4409947 GSM3294232 SRP154483 SRS3563581 GSM3294232 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294232 GSM3294232 GEO Accession GSM3294232 SRX4409948 GSM3294233 SRP154483 SRS3563580 GSM3294233 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294233 GSM3294233 GEO Accession GSM3294233 SRX4409949 GSM3294234 SRP154483 SRS3563582 GSM3294234 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294234 GSM3294234 GEO Accession GSM3294234 SRX4409950 GSM3294235 SRP154483 SRS3563583 GSM3294235 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294235 GSM3294235 GEO Accession GSM3294235 SRX4409951 GSM3294236 SRP154483 SRS3563585 GSM3294236 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294236 GSM3294236 GEO Accession GSM3294236 SRX4409952 GSM3294237 SRP154483 SRS3563584 GSM3294237 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294237 GSM3294237 GEO Accession GSM3294237 SRX4409953 GSM3294238 SRP154483 SRS3563588 GSM3294238 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294238 GSM3294238 GEO Accession GSM3294238 SRX4409954 GSM3294239 SRP154483 SRS3563586 GSM3294239 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294239 GSM3294239 GEO Accession GSM3294239 SRX4409955 GSM3294240 SRP154483 SRS3563587 GSM3294240 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294240 GSM3294240 GEO Accession GSM3294240 SRX4409956 GSM3294241 SRP154483 SRS3563589 GSM3294241 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294241 GSM3294241 GEO Accession GSM3294241 SRX4409957 GSM3294242 SRP154483 SRS3563590 GSM3294242 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294242 GSM3294242 GEO Accession GSM3294242 SRX4409958 GSM3294243 SRP154483 SRS3563728 GSM3294243 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294243 GSM3294243 GEO Accession GSM3294243 SRX4409959 GSM3294244 SRP154483 SRS3563592 GSM3294244 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294244 GSM3294244 GEO Accession GSM3294244 SRX4409960 GSM3294245 SRP154483 SRS3563593 GSM3294245 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294245 GSM3294245 GEO Accession GSM3294245 SRX4409961 GSM3294246 SRP154483 SRS3563594 GSM3294246 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294246 GSM3294246 GEO Accession GSM3294246 SRX4409962 GSM3294247 SRP154483 SRS3563591 GSM3294247 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294247 GSM3294247 GEO Accession GSM3294247 SRX4409963 GSM3294248 SRP154483 SRS3563595 GSM3294248 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294248 GSM3294248 GEO Accession GSM3294248 SRX4409964 GSM3294249 SRP154483 SRS3563596 GSM3294249 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294249 GSM3294249 GEO Accession GSM3294249 SRX4409965 GSM3294250 SRP154483 SRS3563597 GSM3294250 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294250 GSM3294250 GEO Accession GSM3294250 SRX4409966 GSM3294251 SRP154483 SRS3563598 GSM3294251 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294251 GSM3294251 GEO Accession GSM3294251 SRX4409967 GSM3294252 SRP154483 SRS3563599 GSM3294252 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294252 GSM3294252 GEO Accession GSM3294252 SRX4409968 GSM3294253 SRP154483 SRS3563600 GSM3294253 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294253 GSM3294253 GEO Accession GSM3294253 SRX4409969 GSM3294254 SRP154483 SRS3563602 GSM3294254 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294254 GSM3294254 GEO Accession GSM3294254 SRX4409970 GSM3294255 SRP154483 SRS3563601 GSM3294255 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294255 GSM3294255 GEO Accession GSM3294255 SRX4409971 GSM3294256 SRP154483 SRS3563605 GSM3294256 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294256 GSM3294256 GEO Accession GSM3294256 SRX4409972 GSM3294257 SRP154483 SRS3563603 GSM3294257 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294257 GSM3294257 GEO Accession GSM3294257 SRX4409973 GSM3294258 SRP154483 SRS3563604 GSM3294258 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294258 GSM3294258 GEO Accession GSM3294258 SRX4409974 GSM3294259 SRP154483 SRS3563606 GSM3294259 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294259 GSM3294259 GEO Accession GSM3294259 SRX4409975 GSM3294260 SRP154483 SRS3563607 GSM3294260 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294260 GSM3294260 GEO Accession GSM3294260 SRX4409976 GSM3294261 SRP154483 SRS3563608 GSM3294261 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294261 GSM3294261 GEO Accession GSM3294261 SRX4409977 GSM3294262 SRP154483 SRS3563610 GSM3294262 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294262 GSM3294262 GEO Accession GSM3294262 SRX4409978 GSM3294263 SRP154483 SRS3563612 GSM3294263 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294263 GSM3294263 GEO Accession GSM3294263 SRX4409979 GSM3294264 SRP154483 SRS3563613 GSM3294264 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294264 GSM3294264 GEO Accession GSM3294264 SRX4409980 GSM3294265 SRP154483 SRS3563609 GSM3294265 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294265 GSM3294265 GEO Accession GSM3294265 SRX4409981 GSM3294266 SRP154483 SRS3563611 GSM3294266 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294266 GSM3294266 GEO Accession GSM3294266 SRX4409982 GSM3294267 SRP154483 SRS3563614 GSM3294267 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294267 GSM3294267 GEO Accession GSM3294267 SRX4409983 GSM3294268 SRP154483 SRS3563615 GSM3294268 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294268 GSM3294268 GEO Accession GSM3294268 SRX4409984 GSM3294269 SRP154483 SRS3563616 GSM3294269 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294269 GSM3294269 GEO Accession GSM3294269 SRX4409985 GSM3294270 SRP154483 SRS3563618 GSM3294270 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294270 GSM3294270 GEO Accession GSM3294270 SRX4409986 GSM3294271 SRP154483 SRS3563617 GSM3294271 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294271 GSM3294271 GEO Accession GSM3294271 SRX4409987 GSM3294272 SRP154483 SRS3563619 GSM3294272 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294272 GSM3294272 GEO Accession GSM3294272 SRX4409988 GSM3294273 SRP154483 SRS3563620 GSM3294273 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294273 GSM3294273 GEO Accession GSM3294273 SRX4409989 GSM3294274 SRP154483 SRS3563621 GSM3294274 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294274 GSM3294274 GEO Accession GSM3294274 SRX4409990 GSM3294275 SRP154483 SRS3563622 GSM3294275 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294275 GSM3294275 GEO Accession GSM3294275 SRX4409991 GSM3294276 SRP154483 SRS3563623 GSM3294276 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294276 GSM3294276 GEO Accession GSM3294276 SRX4409992 GSM3294277 SRP154483 SRS3563624 GSM3294277 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294277 GSM3294277 GEO Accession GSM3294277 SRX4409993 GSM3294278 SRP154483 SRS3563626 GSM3294278 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294278 GSM3294278 GEO Accession GSM3294278 SRX4409994 GSM3294279 SRP154483 SRS3563627 GSM3294279 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294279 GSM3294279 GEO Accession GSM3294279 SRX4409995 GSM3294280 SRP154483 SRS3563625 GSM3294280 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294280 GSM3294280 GEO Accession GSM3294280 SRX4409996 GSM3294281 SRP154483 SRS3563628 GSM3294281 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294281 GSM3294281 GEO Accession GSM3294281 SRX4409997 GSM3294282 SRP154483 SRS3563629 GSM3294282 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294282 GSM3294282 GEO Accession GSM3294282 SRX4409998 GSM3294283 SRP154483 SRS3563630 GSM3294283 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294283 GSM3294283 GEO Accession GSM3294283 SRX4409999 GSM3294284 SRP154483 SRS3563633 GSM3294284 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294284 GSM3294284 GEO Accession GSM3294284 SRX4410000 GSM3294285 SRP154483 SRS3563632 GSM3294285 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294285 GSM3294285 GEO Accession GSM3294285 SRX4410001 GSM3294286 SRP154483 SRS3563634 GSM3294286 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294286 GSM3294286 GEO Accession GSM3294286 SRX4410002 GSM3294287 SRP154483 SRS3563635 GSM3294287 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294287 GSM3294287 GEO Accession GSM3294287 SRX4410003 GSM3294288 SRP154483 SRS3563636 GSM3294288 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294288 GSM3294288 GEO Accession GSM3294288 SRX4410004 GSM3294289 SRP154483 SRS3563640 GSM3294289 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294289 GSM3294289 GEO Accession GSM3294289 SRX4410005 GSM3294290 SRP154483 SRS3563637 GSM3294290 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294290 GSM3294290 GEO Accession GSM3294290 SRX4410006 GSM3294291 SRP154483 SRS3563638 GSM3294291 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294291 GSM3294291 GEO Accession GSM3294291 SRX4410007 GSM3294292 SRP154483 SRS3563639 GSM3294292 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294292 GSM3294292 GEO Accession GSM3294292 SRX4410008 GSM3294293 SRP154483 SRS3563641 GSM3294293 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294293 GSM3294293 GEO Accession GSM3294293 SRX4410009 GSM3294294 SRP154483 SRS3563642 GSM3294294 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294294 GSM3294294 GEO Accession GSM3294294 SRX4410010 GSM3294295 SRP154483 SRS3563644 GSM3294295 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294295 GSM3294295 GEO Accession GSM3294295 SRX4410011 GSM3294296 SRP154483 SRS3563643 GSM3294296 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294296 GSM3294296 GEO Accession GSM3294296 SRX4410012 GSM3294297 SRP154483 SRS3563645 GSM3294297 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294297 GSM3294297 GEO Accession GSM3294297 SRX4410013 GSM3294298 SRP154483 SRS3563646 GSM3294298 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294298 GSM3294298 GEO Accession GSM3294298 SRX4410014 GSM3294299 SRP154483 SRS3563647 GSM3294299 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294299 GSM3294299 GEO Accession GSM3294299 SRX4410015 GSM3294300 SRP154483 SRS3563648 GSM3294300 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294300 GSM3294300 GEO Accession GSM3294300 SRX4410016 GSM3294301 SRP154483 SRS3563649 GSM3294301 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294301 GSM3294301 GEO Accession GSM3294301 SRX4410017 GSM3294302 SRP154483 SRS3563650 GSM3294302 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294302 GSM3294302 GEO Accession GSM3294302 SRX4410018 GSM3294303 SRP154483 SRS3563652 GSM3294303 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294303 GSM3294303 GEO Accession GSM3294303 SRX4410019 GSM3294304 SRP154483 SRS3563651 GSM3294304 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294304 GSM3294304 GEO Accession GSM3294304 SRX4410020 GSM3294305 SRP154483 SRS3563653 GSM3294305 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294305 GSM3294305 GEO Accession GSM3294305 SRX4410021 GSM3294306 SRP154483 SRS3563654 GSM3294306 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294306 GSM3294306 GEO Accession GSM3294306 SRX4410022 GSM3294307 SRP154483 SRS3563655 GSM3294307 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294307 GSM3294307 GEO Accession GSM3294307 SRX4410023 GSM3294308 SRP154483 SRS3563656 GSM3294308 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294308 GSM3294308 GEO Accession GSM3294308 SRX4410024 GSM3294309 SRP154483 SRS3563657 GSM3294309 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294309 GSM3294309 GEO Accession GSM3294309 SRX4410025 GSM3294310 SRP154483 SRS3563658 GSM3294310 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294310 GSM3294310 GEO Accession GSM3294310 SRX4410026 GSM3294311 SRP154483 SRS3563659 GSM3294311 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294311 GSM3294311 GEO Accession GSM3294311 SRX4410027 GSM3294312 SRP154483 SRS3563660 GSM3294312 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294312 GSM3294312 GEO Accession GSM3294312 SRX4410028 GSM3294313 SRP154483 SRS3563661 GSM3294313 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294313 GSM3294313 GEO Accession GSM3294313 SRX4410029 GSM3294314 SRP154483 SRS3563662 GSM3294314 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294314 GSM3294314 GEO Accession GSM3294314 SRX4410030 GSM3294315 SRP154483 SRS3563663 GSM3294315 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294315 GSM3294315 GEO Accession GSM3294315 SRX4410031 GSM3294316 SRP154483 SRS3563666 GSM3294316 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294316 GSM3294316 GEO Accession GSM3294316 SRX4410032 GSM3294317 SRP154483 SRS3563664 GSM3294317 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294317 GSM3294317 GEO Accession GSM3294317 SRX4410033 GSM3294318 SRP154483 SRS3563668 GSM3294318 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294318 GSM3294318 GEO Accession GSM3294318 SRX4410034 GSM3294319 SRP154483 SRS3563665 GSM3294319 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294319 GSM3294319 GEO Accession GSM3294319 SRX4410035 GSM3294320 SRP154483 SRS3563667 GSM3294320 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294320 GSM3294320 GEO Accession GSM3294320 SRX4410036 GSM3294321 SRP154483 SRS3563669 GSM3294321 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294321 GSM3294321 GEO Accession GSM3294321 SRX4410037 GSM3294322 SRP154483 SRS3563670 GSM3294322 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294322 GSM3294322 GEO Accession GSM3294322 SRX4410038 GSM3294323 SRP154483 SRS3563672 GSM3294323 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294323 GSM3294323 GEO Accession GSM3294323 SRX4410039 GSM3294324 SRP154483 SRS3563673 GSM3294324 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294324 GSM3294324 GEO Accession GSM3294324 SRX4410040 GSM3294325 SRP154483 SRS3563674 GSM3294325 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294325 GSM3294325 GEO Accession GSM3294325 SRX4410041 GSM3294326 SRP154483 SRS3563671 GSM3294326 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294326 GSM3294326 GEO Accession GSM3294326 SRX4410042 GSM3294327 SRP154483 SRS3563675 GSM3294327 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294327 GSM3294327 GEO Accession GSM3294327 SRX4410043 GSM3294328 SRP154483 SRS3563677 GSM3294328 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294328 GSM3294328 GEO Accession GSM3294328 SRX4410044 GSM3294329 SRP154483 SRS3563676 GSM3294329 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294329 GSM3294329 GEO Accession GSM3294329 SRX4410045 GSM3294330 SRP154483 SRS3563680 GSM3294330 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294330 GSM3294330 GEO Accession GSM3294330 SRX4410046 GSM3294331 SRP154483 SRS3563678 GSM3294331 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294331 GSM3294331 GEO Accession GSM3294331 SRX4410047 GSM3294332 SRP154483 SRS3563679 GSM3294332 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294332 GSM3294332 GEO Accession GSM3294332 SRX4410048 GSM3294333 SRP154483 SRS3563681 GSM3294333 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294333 GSM3294333 GEO Accession GSM3294333 SRX4410049 GSM3294334 SRP154483 SRS3563683 GSM3294334 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294334 GSM3294334 GEO Accession GSM3294334 SRX4410050 GSM3294335 SRP154483 SRS3563682 GSM3294335 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294335 GSM3294335 GEO Accession GSM3294335 SRX4410051 GSM3294336 SRP154483 SRS3563685 GSM3294336 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294336 GSM3294336 GEO Accession GSM3294336 SRX4410052 GSM3294337 SRP154483 SRS3563684 GSM3294337 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294337 GSM3294337 GEO Accession GSM3294337 SRX4410053 GSM3294338 SRP154483 SRS3563686 GSM3294338 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294338 GSM3294338 GEO Accession GSM3294338 SRX4410054 GSM3294339 SRP154483 SRS3563687 GSM3294339 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294339 GSM3294339 GEO Accession GSM3294339 SRX4410055 GSM3294340 SRP154483 SRS3563688 GSM3294340 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294340 GSM3294340 GEO Accession GSM3294340 SRX4410056 GSM3294341 SRP154483 SRS3563691 GSM3294341 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294341 GSM3294341 GEO Accession GSM3294341 SRX4410057 GSM3294342 SRP154483 SRS3563692 GSM3294342 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294342 GSM3294342 GEO Accession GSM3294342 SRX4410058 GSM3294343 SRP154483 SRS3563690 GSM3294343 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294343 GSM3294343 GEO Accession GSM3294343 SRX4410059 GSM3294344 SRP154483 SRS3563689 GSM3294344 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294344 GSM3294344 GEO Accession GSM3294344 SRX4410060 GSM3294345 SRP154483 SRS3563693 GSM3294345 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294345 GSM3294345 GEO Accession GSM3294345 SRX4410061 GSM3294346 SRP154483 SRS3563694 GSM3294346 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294346 GSM3294346 GEO Accession GSM3294346 SRX4410062 GSM3294347 SRP154483 SRS3563695 GSM3294347 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294347 GSM3294347 GEO Accession GSM3294347 SRX4410063 GSM3294348 SRP154483 SRS3563696 GSM3294348 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294348 GSM3294348 GEO Accession GSM3294348 SRX4410064 GSM3294349 SRP154483 SRS3563697 GSM3294349 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294349 GSM3294349 GEO Accession GSM3294349 SRX4410065 GSM3294350 SRP154483 SRS3563698 GSM3294350 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294350 GSM3294350 GEO Accession GSM3294350 SRX4410066 GSM3294351 SRP154483 SRS3563699 GSM3294351 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294351 GSM3294351 GEO Accession GSM3294351 SRX4410067 GSM3294352 SRP154483 SRS3563701 GSM3294352 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294352 GSM3294352 GEO Accession GSM3294352 SRX4410068 GSM3294353 SRP154483 SRS3563700 GSM3294353 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294353 GSM3294353 GEO Accession GSM3294353 SRX4410069 GSM3294354 SRP154483 SRS3563702 GSM3294354 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294354 GSM3294354 GEO Accession GSM3294354 SRX4410070 GSM3294355 SRP154483 SRS3563704 GSM3294355 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294355 GSM3294355 GEO Accession GSM3294355 SRX4410071 GSM3294356 SRP154483 SRS3563703 GSM3294356 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294356 GSM3294356 GEO Accession GSM3294356 SRX4410072 GSM3294357 SRP154483 SRS3563706 GSM3294357 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294357 GSM3294357 GEO Accession GSM3294357 SRX4410073 GSM3294358 SRP154483 SRS3563705 GSM3294358 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294358 GSM3294358 GEO Accession GSM3294358 SRX4410074 GSM3294359 SRP154483 SRS3563709 GSM3294359 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294359 GSM3294359 GEO Accession GSM3294359 SRX4410075 GSM3294360 SRP154483 SRS3563708 GSM3294360 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294360 GSM3294360 GEO Accession GSM3294360 SRX4410076 GSM3294361 SRP154483 SRS3563710 GSM3294361 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294361 GSM3294361 GEO Accession GSM3294361 SRX4410077 GSM3294362 SRP154483 SRS3563707 GSM3294362 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294362 GSM3294362 GEO Accession GSM3294362 SRX4410078 GSM3294363 SRP154483 SRS3563714 GSM3294363 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294363 GSM3294363 GEO Accession GSM3294363 SRX4410079 GSM3294364 SRP154483 SRS3563712 GSM3294364 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294364 GSM3294364 GEO Accession GSM3294364 SRX4410080 GSM3294365 SRP154483 SRS3563713 GSM3294365 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294365 GSM3294365 GEO Accession GSM3294365 SRX4410081 GSM3294366 SRP154483 SRS3563711 GSM3294366 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294366 GSM3294366 GEO Accession GSM3294366 SRX4410082 GSM3294367 SRP154483 SRS3563716 GSM3294367 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294367 GSM3294367 GEO Accession GSM3294367 SRX4410083 GSM3294368 SRP154483 SRS3563715 GSM3294368 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294368 GSM3294368 GEO Accession GSM3294368 SRX4410084 GSM3294369 SRP154483 SRS3563718 GSM3294369 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294369 GSM3294369 GEO Accession GSM3294369 SRX4410085 GSM3294370 SRP154483 SRS3563717 GSM3294370 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294370 GSM3294370 GEO Accession GSM3294370 SRX4410086 GSM3294371 SRP154483 SRS3563720 GSM3294371 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294371 GSM3294371 GEO Accession GSM3294371 SRX4410087 GSM3294372 SRP154483 SRS3563719 GSM3294372 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294372 GSM3294372 GEO Accession GSM3294372 SRX4410088 GSM3294373 SRP154483 SRS3563721 GSM3294373 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294373 GSM3294373 GEO Accession GSM3294373 SRX4410089 GSM3294374 SRP154483 SRS3563722 GSM3294374 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294374 GSM3294374 GEO Accession GSM3294374 SRX4410090 GSM3294375 SRP154483 SRS3563723 GSM3294375 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294375 GSM3294375 GEO Accession GSM3294375 SRX4410091 GSM3294376 SRP154483 SRS3563726 GSM3294376 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294376 GSM3294376 GEO Accession GSM3294376 SRX4410092 GSM3294377 SRP154483 SRS3563724 GSM3294377 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294377 GSM3294377 GEO Accession GSM3294377 SRX4410093 GSM3294378 SRP154483 SRS3563725 GSM3294378 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294378 GSM3294378 GEO Accession GSM3294378 SRX4410094 GSM3294379 SRP154483 SRS3563727 GSM3294379 RNA-Seq TRANSCRIPTOMIC cDNA Priming of the 17-25µm (large) IFC plate (Fluidigm, 100-5761) was completed according to the manufacturer's instructions. Following priming, 15µL of cell mix was added to the IFC plate along with LIVE/DEAD cell staining solution containing 4µM ethidium homodimer-1 and calcein AM (Life Technologies, L-3224). Cells were isolated and stained within the C1 system and then manually observed on an inverted fluorescence microscope with FITC and Texas Red filters (Olympus IX51). Capture sites containing 0 or >1 cell were excluded, and cells with positive ethidium homodimer-1 staining were also excluded. Cell lysis, reverse transcription, and cDNA amplification of single cells were conducted following the protocol for mRNA sequencing (Fluidigm). RNA sequencing by Illumina HiSeq2500 next generation sequencer Illumina HiSeq 2500 gds 303294379 GSM3294379 GEO Accession GSM3294379