SRX3823370 GSM3056938 SRP136067 SRS3072892 GSM3056938 RNA-Seq TRANSCRIPTOMIC cDNA Cells were directly sorted into the lysis buffer and follow the modified the protocol initially developed for single-cell RNA-seq (Tang, 2011) to accommodate 100-200 sorted cells by doubling reaction volumes with extra buffers until the step for second strand DNA synthesis RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303056938 GSM3056938 GEO Accession GSM3056938 SRX3823371 GSM3056939 SRP136067 SRS3072891 GSM3056939 RNA-Seq TRANSCRIPTOMIC cDNA Cells were directly sorted into the lysis buffer and follow the modified the protocol initially developed for single-cell RNA-seq (Tang, 2011) to accommodate 100-200 sorted cells by doubling reaction volumes with extra buffers until the step for second strand DNA synthesis RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303056939 GSM3056939 GEO Accession GSM3056939 SRX3823372 GSM3056940 SRP136067 SRS3072893 GSM3056940 RNA-Seq TRANSCRIPTOMIC cDNA Cells were directly sorted into the lysis buffer and follow the modified the protocol initially developed for single-cell RNA-seq (Tang, 2011) to accommodate 100-200 sorted cells by doubling reaction volumes with extra buffers until the step for second strand DNA synthesis RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303056940 GSM3056940 GEO Accession GSM3056940 SRX3823373 GSM3056941 SRP136067 SRS3072894 GSM3056941 RNA-Seq TRANSCRIPTOMIC cDNA Cells were directly sorted into the lysis buffer and follow the modified the protocol initially developed for single-cell RNA-seq (Tang, 2011) to accommodate 100-200 sorted cells by doubling reaction volumes with extra buffers until the step for second strand DNA synthesis RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303056941 GSM3056941 GEO Accession GSM3056941 SRX3823374 GSM3056942 SRP136067 SRS3072896 GSM3056942 RNA-Seq TRANSCRIPTOMIC cDNA Cells were directly sorted into the lysis buffer and follow the modified the protocol initially developed for single-cell RNA-seq (Tang, 2011) to accommodate 100-200 sorted cells by doubling reaction volumes with extra buffers until the step for second strand DNA synthesis RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303056942 GSM3056942 GEO Accession GSM3056942 SRX3823375 GSM3056943 SRP136067 SRS3072895 GSM3056943 RNA-Seq TRANSCRIPTOMIC cDNA Cells were directly sorted into the lysis buffer and follow the modified the protocol initially developed for single-cell RNA-seq (Tang, 2011) to accommodate 100-200 sorted cells by doubling reaction volumes with extra buffers until the step for second strand DNA synthesis RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303056943 GSM3056943 GEO Accession GSM3056943 SRX3823376 GSM3056944 SRP136067 SRS3072897 GSM3056944 RNA-Seq TRANSCRIPTOMIC cDNA Cells were directly sorted into the lysis buffer and follow the modified the protocol initially developed for single-cell RNA-seq (Tang, 2011) to accommodate 100-200 sorted cells by doubling reaction volumes with extra buffers until the step for second strand DNA synthesis RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303056944 GSM3056944 GEO Accession GSM3056944 SRX3823377 GSM3056945 SRP136067 SRS3072898 GSM3056945 RNA-Seq TRANSCRIPTOMIC cDNA Cells were directly sorted into the lysis buffer and follow the modified the protocol initially developed for single-cell RNA-seq (Tang, 2011) to accommodate 100-200 sorted cells by doubling reaction volumes with extra buffers until the step for second strand DNA synthesis RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303056945 GSM3056945 GEO Accession GSM3056945 SRX3823378 GSM3056946 SRP136067 SRS3072899 GSM3056946 RNA-Seq TRANSCRIPTOMIC cDNA Cells were directly sorted into the lysis buffer and follow the modified the protocol initially developed for single-cell RNA-seq (Tang, 2011) to accommodate 100-200 sorted cells by doubling reaction volumes with extra buffers until the step for second strand DNA synthesis RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303056946 GSM3056946 GEO Accession GSM3056946 SRX3823379 GSM3056947 SRP136067 SRS3072900 GSM3056947 RNA-Seq TRANSCRIPTOMIC cDNA Cells were directly sorted into the lysis buffer and follow the modified the protocol initially developed for single-cell RNA-seq (Tang, 2011) to accommodate 100-200 sorted cells by doubling reaction volumes with extra buffers until the step for second strand DNA synthesis RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303056947 GSM3056947 GEO Accession GSM3056947 SRX3823380 GSM3056948 SRP136067 SRS3072901 GSM3056948 RNA-Seq TRANSCRIPTOMIC cDNA Cells were directly sorted into the lysis buffer and follow the modified the protocol initially developed for single-cell RNA-seq (Tang, 2011) to accommodate 100-200 sorted cells by doubling reaction volumes with extra buffers until the step for second strand DNA synthesis RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303056948 GSM3056948 GEO Accession GSM3056948 SRX3823381 GSM3056949 SRP136067 SRS3072902 GSM3056949 RNA-Seq TRANSCRIPTOMIC cDNA Cells were directly sorted into the lysis buffer and follow the modified the protocol initially developed for single-cell RNA-seq (Tang, 2011) to accommodate 100-200 sorted cells by doubling reaction volumes with extra buffers until the step for second strand DNA synthesis RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303056949 GSM3056949 GEO Accession GSM3056949