SRX6044218 GSM3874940 SRP201124 SRS4947343 GSM3874940 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874940 GSM3874940 GEO Accession GSM3874940 SRX6044219 GSM3874941 SRP201124 SRS4947344 GSM3874941 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874941 GSM3874941 GEO Accession GSM3874941 SRX6044220 GSM3874942 SRP201124 SRS4947345 GSM3874942 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874942 GSM3874942 GEO Accession GSM3874942 SRX6044221 GSM3874943 SRP201124 SRS4947346 GSM3874943 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874943 GSM3874943 GEO Accession GSM3874943 SRX6044222 GSM3874944 SRP201124 SRS4947347 GSM3874944 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874944 GSM3874944 GEO Accession GSM3874944 SRX6044223 GSM3874945 SRP201124 SRS4947348 GSM3874945 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874945 GSM3874945 GEO Accession GSM3874945 SRX6044224 GSM3874946 SRP201124 SRS4947349 GSM3874946 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874946 GSM3874946 GEO Accession GSM3874946 SRX6044225 GSM3874947 SRP201124 SRS4947350 GSM3874947 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874947 GSM3874947 GEO Accession GSM3874947 SRX6044226 GSM3874948 SRP201124 SRS4947351 GSM3874948 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874948 GSM3874948 GEO Accession GSM3874948 SRX6044227 GSM3874949 SRP201124 SRS4947352 GSM3874949 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874949 GSM3874949 GEO Accession GSM3874949 SRX6044228 GSM3874950 SRP201124 SRS4947353 GSM3874950 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874950 GSM3874950 GEO Accession GSM3874950 SRX6044229 GSM3874730 SRP201124 SRS4947354 GSM3874730 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874730 GSM3874730 GEO Accession GSM3874730 SRX6044230 GSM3874731 SRP201124 SRS4947355 GSM3874731 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874731 GSM3874731 GEO Accession GSM3874731 SRX6044231 GSM3874732 SRP201124 SRS4947356 GSM3874732 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874732 GSM3874732 GEO Accession GSM3874732 SRX6044232 GSM3874733 SRP201124 SRS4947357 GSM3874733 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874733 GSM3874733 GEO Accession GSM3874733 SRX6044233 GSM3874734 SRP201124 SRS4947358 GSM3874734 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874734 GSM3874734 GEO Accession GSM3874734 SRX6044234 GSM3874735 SRP201124 SRS4947359 GSM3874735 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874735 GSM3874735 GEO Accession GSM3874735 SRX6044235 GSM3874736 SRP201124 SRS4947360 GSM3874736 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874736 GSM3874736 GEO Accession GSM3874736 SRX6044236 GSM3874737 SRP201124 SRS4947361 GSM3874737 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874737 GSM3874737 GEO Accession GSM3874737 SRX6044238 GSM3874738 SRP201124 SRS4947363 GSM3874738 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874738 GSM3874738 GEO Accession GSM3874738 SRX6044239 GSM3874739 SRP201124 SRS4947364 GSM3874739 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874739 GSM3874739 GEO Accession GSM3874739 SRX6044240 GSM3874740 SRP201124 SRS4947365 GSM3874740 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874740 GSM3874740 GEO Accession GSM3874740 SRX6044241 GSM3874741 SRP201124 SRS4947366 GSM3874741 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874741 GSM3874741 GEO Accession GSM3874741 SRX6044242 GSM3874742 SRP201124 SRS4947367 GSM3874742 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874742 GSM3874742 GEO Accession GSM3874742 SRX6044243 GSM3874743 SRP201124 SRS4947368 GSM3874743 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874743 GSM3874743 GEO Accession GSM3874743 SRX6044244 GSM3874744 SRP201124 SRS4947369 GSM3874744 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874744 GSM3874744 GEO Accession GSM3874744 SRX6044245 GSM3874745 SRP201124 SRS4947370 GSM3874745 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874745 GSM3874745 GEO Accession GSM3874745 SRX6044246 GSM3874746 SRP201124 SRS4947371 GSM3874746 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874746 GSM3874746 GEO Accession GSM3874746 SRX6044247 GSM3874747 SRP201124 SRS4947372 GSM3874747 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874747 GSM3874747 GEO Accession GSM3874747 SRX6044248 GSM3874748 SRP201124 SRS4947373 GSM3874748 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874748 GSM3874748 GEO Accession GSM3874748 SRX6044249 GSM3874749 SRP201124 SRS4947374 GSM3874749 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874749 GSM3874749 GEO Accession GSM3874749 SRX6044250 GSM3874750 SRP201124 SRS4947375 GSM3874750 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874750 GSM3874750 GEO Accession GSM3874750 SRX6044251 GSM3874751 SRP201124 SRS4947376 GSM3874751 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874751 GSM3874751 GEO Accession GSM3874751 SRX6044252 GSM3874752 SRP201124 SRS4947377 GSM3874752 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874752 GSM3874752 GEO Accession GSM3874752 SRX6044253 GSM3874753 SRP201124 SRS4947378 GSM3874753 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874753 GSM3874753 GEO Accession GSM3874753 SRX6044254 GSM3874754 SRP201124 SRS4947379 GSM3874754 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874754 GSM3874754 GEO Accession GSM3874754 SRX6044255 GSM3874755 SRP201124 SRS4947380 GSM3874755 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874755 GSM3874755 GEO Accession GSM3874755 SRX6044256 GSM3874756 SRP201124 SRS4947381 GSM3874756 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874756 GSM3874756 GEO Accession GSM3874756 SRX6044257 GSM3874757 SRP201124 SRS4947383 GSM3874757 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874757 GSM3874757 GEO Accession GSM3874757 SRX6044258 GSM3874758 SRP201124 SRS4947382 GSM3874758 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874758 GSM3874758 GEO Accession GSM3874758 SRX6044259 GSM3874759 SRP201124 SRS4947384 GSM3874759 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874759 GSM3874759 GEO Accession GSM3874759 SRX6044260 GSM3874760 SRP201124 SRS4947385 GSM3874760 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874760 GSM3874760 GEO Accession GSM3874760 SRX6044261 GSM3874761 SRP201124 SRS4947386 GSM3874761 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874761 GSM3874761 GEO Accession GSM3874761 SRX6044262 GSM3874762 SRP201124 SRS4947387 GSM3874762 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874762 GSM3874762 GEO Accession GSM3874762 SRX6044263 GSM3874763 SRP201124 SRS4947388 GSM3874763 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874763 GSM3874763 GEO Accession GSM3874763 SRX6044264 GSM3874764 SRP201124 SRS4947390 GSM3874764 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874764 GSM3874764 GEO Accession GSM3874764 SRX6044265 GSM3874765 SRP201124 SRS4947389 GSM3874765 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874765 GSM3874765 GEO Accession GSM3874765 SRX6044266 GSM3874766 SRP201124 SRS4947391 GSM3874766 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874766 GSM3874766 GEO Accession GSM3874766 SRX6044268 GSM3874767 SRP201124 SRS4947393 GSM3874767 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874767 GSM3874767 GEO Accession GSM3874767 SRX6044269 GSM3874768 SRP201124 SRS4947395 GSM3874768 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874768 GSM3874768 GEO Accession GSM3874768 SRX6044270 GSM3874769 SRP201124 SRS4947394 GSM3874769 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874769 GSM3874769 GEO Accession GSM3874769 SRX6044271 GSM3874770 SRP201124 SRS4947396 GSM3874770 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874770 GSM3874770 GEO Accession GSM3874770 SRX6044272 GSM3874771 SRP201124 SRS4947397 GSM3874771 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874771 GSM3874771 GEO Accession GSM3874771 SRX6044273 GSM3874772 SRP201124 SRS4947398 GSM3874772 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874772 GSM3874772 GEO Accession GSM3874772 SRX6044274 GSM3874773 SRP201124 SRS4947400 GSM3874773 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874773 GSM3874773 GEO Accession GSM3874773 SRX6044275 GSM3874774 SRP201124 SRS4947399 GSM3874774 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874774 GSM3874774 GEO Accession GSM3874774 SRX6044276 GSM3874775 SRP201124 SRS4947401 GSM3874775 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874775 GSM3874775 GEO Accession GSM3874775 SRX6044277 GSM3874776 SRP201124 SRS4947402 GSM3874776 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874776 GSM3874776 GEO Accession GSM3874776 SRX6044278 GSM3874777 SRP201124 SRS4947403 GSM3874777 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874777 GSM3874777 GEO Accession GSM3874777 SRX6044279 GSM3874778 SRP201124 SRS4947404 GSM3874778 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874778 GSM3874778 GEO Accession GSM3874778 SRX6044280 GSM3874779 SRP201124 SRS4947405 GSM3874779 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874779 GSM3874779 GEO Accession GSM3874779 SRX6044281 GSM3874780 SRP201124 SRS4947407 GSM3874780 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874780 GSM3874780 GEO Accession GSM3874780 SRX6044282 GSM3874781 SRP201124 SRS4947406 GSM3874781 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874781 GSM3874781 GEO Accession GSM3874781 SRX6044283 GSM3874782 SRP201124 SRS4947408 GSM3874782 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874782 GSM3874782 GEO Accession GSM3874782 SRX6044284 GSM3874783 SRP201124 SRS4947409 GSM3874783 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874783 GSM3874783 GEO Accession GSM3874783 SRX6044285 GSM3874784 SRP201124 SRS4947410 GSM3874784 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874784 GSM3874784 GEO Accession GSM3874784 SRX6044286 GSM3874785 SRP201124 SRS4947411 GSM3874785 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874785 GSM3874785 GEO Accession GSM3874785 SRX6044287 GSM3874786 SRP201124 SRS4947412 GSM3874786 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874786 GSM3874786 GEO Accession GSM3874786 SRX6044288 GSM3874787 SRP201124 SRS4947413 GSM3874787 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874787 GSM3874787 GEO Accession GSM3874787 SRX6044289 GSM3874788 SRP201124 SRS4947414 GSM3874788 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874788 GSM3874788 GEO Accession GSM3874788 SRX6044290 GSM3874789 SRP201124 SRS4947415 GSM3874789 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874789 GSM3874789 GEO Accession GSM3874789 SRX6044291 GSM3874790 SRP201124 SRS4947416 GSM3874790 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874790 GSM3874790 GEO Accession GSM3874790 SRX6044292 GSM3874791 SRP201124 SRS4947417 GSM3874791 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874791 GSM3874791 GEO Accession GSM3874791 SRX6044293 GSM3874792 SRP201124 SRS4947418 GSM3874792 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874792 GSM3874792 GEO Accession GSM3874792 SRX6044294 GSM3874793 SRP201124 SRS4947420 GSM3874793 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874793 GSM3874793 GEO Accession GSM3874793 SRX6044295 GSM3874794 SRP201124 SRS4947419 GSM3874794 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874794 GSM3874794 GEO Accession GSM3874794 SRX6044296 GSM3874795 SRP201124 SRS4947421 GSM3874795 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874795 GSM3874795 GEO Accession GSM3874795 SRX6044297 GSM3874796 SRP201124 SRS4947422 GSM3874796 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874796 GSM3874796 GEO Accession GSM3874796 SRX6044299 GSM3874797 SRP201124 SRS4947424 GSM3874797 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874797 GSM3874797 GEO Accession GSM3874797 SRX6044300 GSM3874798 SRP201124 SRS4947425 GSM3874798 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874798 GSM3874798 GEO Accession GSM3874798 SRX6044301 GSM3874799 SRP201124 SRS4947426 GSM3874799 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874799 GSM3874799 GEO Accession GSM3874799 SRX6044302 GSM3874800 SRP201124 SRS4947427 GSM3874800 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874800 GSM3874800 GEO Accession GSM3874800 SRX6044303 GSM3874801 SRP201124 SRS4947428 GSM3874801 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874801 GSM3874801 GEO Accession GSM3874801 SRX6044304 GSM3874802 SRP201124 SRS4947429 GSM3874802 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874802 GSM3874802 GEO Accession GSM3874802 SRX6044305 GSM3874803 SRP201124 SRS4947431 GSM3874803 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874803 GSM3874803 GEO Accession GSM3874803 SRX6044306 GSM3874804 SRP201124 SRS4947430 GSM3874804 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874804 GSM3874804 GEO Accession GSM3874804 SRX6044307 GSM3874805 SRP201124 SRS4947432 GSM3874805 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874805 GSM3874805 GEO Accession GSM3874805 SRX6044308 GSM3874806 SRP201124 SRS4947433 GSM3874806 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874806 GSM3874806 GEO Accession GSM3874806 SRX6044309 GSM3874807 SRP201124 SRS4947434 GSM3874807 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874807 GSM3874807 GEO Accession GSM3874807 SRX6044310 GSM3874808 SRP201124 SRS4947435 GSM3874808 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874808 GSM3874808 GEO Accession GSM3874808 SRX6044311 GSM3874809 SRP201124 SRS4947436 GSM3874809 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874809 GSM3874809 GEO Accession GSM3874809 SRX6044312 GSM3874810 SRP201124 SRS4947437 GSM3874810 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874810 GSM3874810 GEO Accession GSM3874810 SRX6044313 GSM3874811 SRP201124 SRS4947438 GSM3874811 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874811 GSM3874811 GEO Accession GSM3874811 SRX6044314 GSM3874812 SRP201124 SRS4947439 GSM3874812 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874812 GSM3874812 GEO Accession GSM3874812 SRX6044315 GSM3874813 SRP201124 SRS4947441 GSM3874813 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874813 GSM3874813 GEO Accession GSM3874813 SRX6044316 GSM3874814 SRP201124 SRS4947440 GSM3874814 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874814 GSM3874814 GEO Accession GSM3874814 SRX6044317 GSM3874815 SRP201124 SRS4947442 GSM3874815 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874815 GSM3874815 GEO Accession GSM3874815 SRX6044318 GSM3874816 SRP201124 SRS4947443 GSM3874816 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874816 GSM3874816 GEO Accession GSM3874816 SRX6044319 GSM3874817 SRP201124 SRS4947444 GSM3874817 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874817 GSM3874817 GEO Accession GSM3874817 SRX6044320 GSM3874818 SRP201124 SRS4947445 GSM3874818 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874818 GSM3874818 GEO Accession GSM3874818 SRX6044321 GSM3874819 SRP201124 SRS4947446 GSM3874819 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874819 GSM3874819 GEO Accession GSM3874819 SRX6044322 GSM3874820 SRP201124 SRS4947447 GSM3874820 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874820 GSM3874820 GEO Accession GSM3874820 SRX6044323 GSM3874821 SRP201124 SRS4947448 GSM3874821 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874821 GSM3874821 GEO Accession GSM3874821 SRX6044324 GSM3874822 SRP201124 SRS4947449 GSM3874822 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874822 GSM3874822 GEO Accession GSM3874822 SRX6044325 GSM3874823 SRP201124 SRS4947450 GSM3874823 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874823 GSM3874823 GEO Accession GSM3874823 SRX6044326 GSM3874824 SRP201124 SRS4947451 GSM3874824 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874824 GSM3874824 GEO Accession GSM3874824 SRX6044328 GSM3874825 SRP201124 SRS4947453 GSM3874825 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874825 GSM3874825 GEO Accession GSM3874825 SRX6044329 GSM3874826 SRP201124 SRS4947454 GSM3874826 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874826 GSM3874826 GEO Accession GSM3874826 SRX6044330 GSM3874827 SRP201124 SRS4947455 GSM3874827 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874827 GSM3874827 GEO Accession GSM3874827 SRX6044331 GSM3874828 SRP201124 SRS4947456 GSM3874828 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874828 GSM3874828 GEO Accession GSM3874828 SRX6044332 GSM3874829 SRP201124 SRS4947458 GSM3874829 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874829 GSM3874829 GEO Accession GSM3874829 SRX6044333 GSM3874830 SRP201124 SRS4947457 GSM3874830 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874830 GSM3874830 GEO Accession GSM3874830 SRX6044334 GSM3874831 SRP201124 SRS4947459 GSM3874831 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874831 GSM3874831 GEO Accession GSM3874831 SRX6044335 GSM3874832 SRP201124 SRS4947460 GSM3874832 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874832 GSM3874832 GEO Accession GSM3874832 SRX6044336 GSM3874833 SRP201124 SRS4947461 GSM3874833 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874833 GSM3874833 GEO Accession GSM3874833 SRX6044337 GSM3874834 SRP201124 SRS4947462 GSM3874834 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874834 GSM3874834 GEO Accession GSM3874834 SRX6044338 GSM3874835 SRP201124 SRS4947463 GSM3874835 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874835 GSM3874835 GEO Accession GSM3874835 SRX6044339 GSM3874836 SRP201124 SRS4947464 GSM3874836 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874836 GSM3874836 GEO Accession GSM3874836 SRX6044340 GSM3874837 SRP201124 SRS4947465 GSM3874837 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874837 GSM3874837 GEO Accession GSM3874837 SRX6044341 GSM3874838 SRP201124 SRS4947467 GSM3874838 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874838 GSM3874838 GEO Accession GSM3874838 SRX6044342 GSM3874839 SRP201124 SRS4947466 GSM3874839 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874839 GSM3874839 GEO Accession GSM3874839 SRX6044343 GSM3874840 SRP201124 SRS4947468 GSM3874840 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874840 GSM3874840 GEO Accession GSM3874840 SRX6044344 GSM3874841 SRP201124 SRS4947469 GSM3874841 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874841 GSM3874841 GEO Accession GSM3874841 SRX6044345 GSM3874842 SRP201124 SRS4947470 GSM3874842 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874842 GSM3874842 GEO Accession GSM3874842 SRX6044346 GSM3874843 SRP201124 SRS4947471 GSM3874843 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874843 GSM3874843 GEO Accession GSM3874843 SRX6044347 GSM3874844 SRP201124 SRS4947472 GSM3874844 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874844 GSM3874844 GEO Accession GSM3874844 SRX6044348 GSM3874845 SRP201124 SRS4947474 GSM3874845 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874845 GSM3874845 GEO Accession GSM3874845 SRX6044349 GSM3874846 SRP201124 SRS4947473 GSM3874846 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874846 GSM3874846 GEO Accession GSM3874846 SRX6044350 GSM3874847 SRP201124 SRS4947475 GSM3874847 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874847 GSM3874847 GEO Accession GSM3874847 SRX6044351 GSM3874848 SRP201124 SRS4947476 GSM3874848 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874848 GSM3874848 GEO Accession GSM3874848 SRX6044352 GSM3874849 SRP201124 SRS4947477 GSM3874849 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874849 GSM3874849 GEO Accession GSM3874849 SRX6044354 GSM3874850 SRP201124 SRS4947479 GSM3874850 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874850 GSM3874850 GEO Accession GSM3874850 SRX6044355 GSM3874851 SRP201124 SRS4947481 GSM3874851 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874851 GSM3874851 GEO Accession GSM3874851 SRX6044356 GSM3874852 SRP201124 SRS4947480 GSM3874852 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874852 GSM3874852 GEO Accession GSM3874852 SRX6044357 GSM3874853 SRP201124 SRS4947482 GSM3874853 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874853 GSM3874853 GEO Accession GSM3874853 SRX6044358 GSM3874854 SRP201124 SRS4947483 GSM3874854 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874854 GSM3874854 GEO Accession GSM3874854 SRX6044359 GSM3874855 SRP201124 SRS4947484 GSM3874855 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874855 GSM3874855 GEO Accession GSM3874855 SRX6044360 GSM3874856 SRP201124 SRS4947485 GSM3874856 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874856 GSM3874856 GEO Accession GSM3874856 SRX6044361 GSM3874857 SRP201124 SRS4947486 GSM3874857 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874857 GSM3874857 GEO Accession GSM3874857 SRX6044362 GSM3874858 SRP201124 SRS4947487 GSM3874858 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874858 GSM3874858 GEO Accession GSM3874858 SRX6044363 GSM3874859 SRP201124 SRS4947488 GSM3874859 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874859 GSM3874859 GEO Accession GSM3874859 SRX6044364 GSM3874860 SRP201124 SRS4947489 GSM3874860 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874860 GSM3874860 GEO Accession GSM3874860 SRX6044365 GSM3874861 SRP201124 SRS4947491 GSM3874861 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874861 GSM3874861 GEO Accession GSM3874861 SRX6044366 GSM3874862 SRP201124 SRS4947490 GSM3874862 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874862 GSM3874862 GEO Accession GSM3874862 SRX6044367 GSM3874863 SRP201124 SRS4947492 GSM3874863 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874863 GSM3874863 GEO Accession GSM3874863 SRX6044368 GSM3874864 SRP201124 SRS4947493 GSM3874864 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874864 GSM3874864 GEO Accession GSM3874864 SRX6044369 GSM3874865 SRP201124 SRS4947494 GSM3874865 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874865 GSM3874865 GEO Accession GSM3874865 SRX6044370 GSM3874866 SRP201124 SRS4947495 GSM3874866 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874866 GSM3874866 GEO Accession GSM3874866 SRX6044371 GSM3874867 SRP201124 SRS4947496 GSM3874867 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874867 GSM3874867 GEO Accession GSM3874867 SRX6044372 GSM3874868 SRP201124 SRS4947497 GSM3874868 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874868 GSM3874868 GEO Accession GSM3874868 SRX6044373 GSM3874869 SRP201124 SRS4947498 GSM3874869 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874869 GSM3874869 GEO Accession GSM3874869 SRX6044374 GSM3874870 SRP201124 SRS4947499 GSM3874870 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874870 GSM3874870 GEO Accession GSM3874870 SRX6044375 GSM3874871 SRP201124 SRS4947500 GSM3874871 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874871 GSM3874871 GEO Accession GSM3874871 SRX6044376 GSM3874872 SRP201124 SRS4947501 GSM3874872 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874872 GSM3874872 GEO Accession GSM3874872 SRX6044377 GSM3874873 SRP201124 SRS4947502 GSM3874873 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874873 GSM3874873 GEO Accession GSM3874873 SRX6044378 GSM3874874 SRP201124 SRS4947503 GSM3874874 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874874 GSM3874874 GEO Accession GSM3874874 SRX6044380 GSM3874875 SRP201124 SRS4947505 GSM3874875 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874875 GSM3874875 GEO Accession GSM3874875 SRX6044381 GSM3874876 SRP201124 SRS4947506 GSM3874876 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874876 GSM3874876 GEO Accession GSM3874876 SRX6044382 GSM3874877 SRP201124 SRS4947507 GSM3874877 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874877 GSM3874877 GEO Accession GSM3874877 SRX6044383 GSM3874878 SRP201124 SRS4947508 GSM3874878 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874878 GSM3874878 GEO Accession GSM3874878 SRX6044384 GSM3874879 SRP201124 SRS4947509 GSM3874879 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874879 GSM3874879 GEO Accession GSM3874879 SRX6044385 GSM3874880 SRP201124 SRS4947510 GSM3874880 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874880 GSM3874880 GEO Accession GSM3874880 SRX6044386 GSM3874881 SRP201124 SRS4947511 GSM3874881 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874881 GSM3874881 GEO Accession GSM3874881 SRX6044387 GSM3874882 SRP201124 SRS4947512 GSM3874882 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874882 GSM3874882 GEO Accession GSM3874882 SRX6044388 GSM3874883 SRP201124 SRS4947513 GSM3874883 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874883 GSM3874883 GEO Accession GSM3874883 SRX6044389 GSM3874884 SRP201124 SRS4947515 GSM3874884 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874884 GSM3874884 GEO Accession GSM3874884 SRX6044390 GSM3874885 SRP201124 SRS4947514 GSM3874885 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874885 GSM3874885 GEO Accession GSM3874885 SRX6044391 GSM3874886 SRP201124 SRS4947516 GSM3874886 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874886 GSM3874886 GEO Accession GSM3874886 SRX6044392 GSM3874887 SRP201124 SRS4947517 GSM3874887 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874887 GSM3874887 GEO Accession GSM3874887 SRX6044393 GSM3874888 SRP201124 SRS4947518 GSM3874888 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874888 GSM3874888 GEO Accession GSM3874888 SRX6044394 GSM3874889 SRP201124 SRS4947519 GSM3874889 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874889 GSM3874889 GEO Accession GSM3874889 SRX6044395 GSM3874890 SRP201124 SRS4947520 GSM3874890 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874890 GSM3874890 GEO Accession GSM3874890 SRX6044396 GSM3874891 SRP201124 SRS4947521 GSM3874891 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874891 GSM3874891 GEO Accession GSM3874891 SRX6044397 GSM3874892 SRP201124 SRS4947522 GSM3874892 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874892 GSM3874892 GEO Accession GSM3874892 SRX6044398 GSM3874893 SRP201124 SRS4947523 GSM3874893 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874893 GSM3874893 GEO Accession GSM3874893 SRX6044399 GSM3874894 SRP201124 SRS4947524 GSM3874894 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874894 GSM3874894 GEO Accession GSM3874894 SRX6044400 GSM3874895 SRP201124 SRS4947525 GSM3874895 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874895 GSM3874895 GEO Accession GSM3874895 SRX6044401 GSM3874896 SRP201124 SRS4947526 GSM3874896 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874896 GSM3874896 GEO Accession GSM3874896 SRX6044402 GSM3874897 SRP201124 SRS4947527 GSM3874897 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874897 GSM3874897 GEO Accession GSM3874897 SRX6044403 GSM3874898 SRP201124 SRS4947528 GSM3874898 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874898 GSM3874898 GEO Accession GSM3874898 SRX6044404 GSM3874899 SRP201124 SRS4947530 GSM3874899 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874899 GSM3874899 GEO Accession GSM3874899 SRX6044405 GSM3874900 SRP201124 SRS4947529 GSM3874900 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874900 GSM3874900 GEO Accession GSM3874900 SRX6044406 GSM3874901 SRP201124 SRS4947531 GSM3874901 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874901 GSM3874901 GEO Accession GSM3874901 SRX6044407 GSM3874902 SRP201124 SRS4947532 GSM3874902 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874902 GSM3874902 GEO Accession GSM3874902 SRX6044408 GSM3874903 SRP201124 SRS4947533 GSM3874903 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874903 GSM3874903 GEO Accession GSM3874903 SRX6044409 GSM3874904 SRP201124 SRS4947534 GSM3874904 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874904 GSM3874904 GEO Accession GSM3874904 SRX6044410 GSM3874905 SRP201124 SRS4947535 GSM3874905 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874905 GSM3874905 GEO Accession GSM3874905 SRX6044412 GSM3874906 SRP201124 SRS4947536 GSM3874906 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874906 GSM3874906 GEO Accession GSM3874906 SRX6044413 GSM3874907 SRP201124 SRS4947538 GSM3874907 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874907 GSM3874907 GEO Accession GSM3874907 SRX6044414 GSM3874908 SRP201124 SRS4947539 GSM3874908 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874908 GSM3874908 GEO Accession GSM3874908 SRX6044415 GSM3874909 SRP201124 SRS4947540 GSM3874909 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874909 GSM3874909 GEO Accession GSM3874909 SRX6044416 GSM3874910 SRP201124 SRS4947541 GSM3874910 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874910 GSM3874910 GEO Accession GSM3874910 SRX6044417 GSM3874911 SRP201124 SRS4947542 GSM3874911 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874911 GSM3874911 GEO Accession GSM3874911 SRX6044418 GSM3874912 SRP201124 SRS4947543 GSM3874912 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874912 GSM3874912 GEO Accession GSM3874912 SRX6044419 GSM3874913 SRP201124 SRS4947544 GSM3874913 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874913 GSM3874913 GEO Accession GSM3874913 SRX6044420 GSM3874914 SRP201124 SRS4947545 GSM3874914 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874914 GSM3874914 GEO Accession GSM3874914 SRX6044421 GSM3874915 SRP201124 SRS4947546 GSM3874915 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874915 GSM3874915 GEO Accession GSM3874915 SRX6044422 GSM3874916 SRP201124 SRS4947547 GSM3874916 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874916 GSM3874916 GEO Accession GSM3874916 SRX6044423 GSM3874917 SRP201124 SRS4947548 GSM3874917 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874917 GSM3874917 GEO Accession GSM3874917 SRX6044424 GSM3874918 SRP201124 SRS4947550 GSM3874918 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874918 GSM3874918 GEO Accession GSM3874918 SRX6044425 GSM3874919 SRP201124 SRS4947549 GSM3874919 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874919 GSM3874919 GEO Accession GSM3874919 SRX6044426 GSM3874920 SRP201124 SRS4947551 GSM3874920 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874920 GSM3874920 GEO Accession GSM3874920 SRX6044427 GSM3874921 SRP201124 SRS4947552 GSM3874921 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874921 GSM3874921 GEO Accession GSM3874921 SRX6044428 GSM3874922 SRP201124 SRS4947553 GSM3874922 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874922 GSM3874922 GEO Accession GSM3874922 SRX6044429 GSM3874923 SRP201124 SRS4947554 GSM3874923 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874923 GSM3874923 GEO Accession GSM3874923 SRX6044430 GSM3874924 SRP201124 SRS4947555 GSM3874924 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874924 GSM3874924 GEO Accession GSM3874924 SRX6044431 GSM3874925 SRP201124 SRS4947556 GSM3874925 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874925 GSM3874925 GEO Accession GSM3874925 SRX6044432 GSM3874926 SRP201124 SRS4947557 GSM3874926 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874926 GSM3874926 GEO Accession GSM3874926 SRX6044433 GSM3874927 SRP201124 SRS4947558 GSM3874927 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874927 GSM3874927 GEO Accession GSM3874927 SRX6044434 GSM3874928 SRP201124 SRS4947559 GSM3874928 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874928 GSM3874928 GEO Accession GSM3874928 SRX6044435 GSM3874929 SRP201124 SRS4947560 GSM3874929 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874929 GSM3874929 GEO Accession GSM3874929 SRX6044436 GSM3874930 SRP201124 SRS4947561 GSM3874930 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874930 GSM3874930 GEO Accession GSM3874930 SRX6044438 GSM3874931 SRP201124 SRS4947563 GSM3874931 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874931 GSM3874931 GEO Accession GSM3874931 SRX6044439 GSM3874932 SRP201124 SRS4947564 GSM3874932 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874932 GSM3874932 GEO Accession GSM3874932 SRX6044440 GSM3874933 SRP201124 SRS4947565 GSM3874933 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874933 GSM3874933 GEO Accession GSM3874933 SRX6044441 GSM3874934 SRP201124 SRS4947566 GSM3874934 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874934 GSM3874934 GEO Accession GSM3874934 SRX6044442 GSM3874935 SRP201124 SRS4947567 GSM3874935 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874935 GSM3874935 GEO Accession GSM3874935 SRX6044443 GSM3874936 SRP201124 SRS4947568 GSM3874936 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874936 GSM3874936 GEO Accession GSM3874936 SRX6044444 GSM3874937 SRP201124 SRS4947569 GSM3874937 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874937 GSM3874937 GEO Accession GSM3874937 SRX6044445 GSM3874938 SRP201124 SRS4947571 GSM3874938 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874938 GSM3874938 GEO Accession GSM3874938 SRX6044446 GSM3874939 SRP201124 SRS4947570 GSM3874939 RNA-Seq TRANSCRIPTOMIC cDNA Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll-Paque (GE Healthcare) density gradient centrifugation of whole blood form a human donor Single cell cDNA libraries were made using the SMARTSeq v2 protocol (Picelli et al., 2014) with the following modification: Use of 200 pg cDNA with 1/5 reaction of Illumina Nextera XT kit (Illumina, San Diego, CA, USA). All samples were subjected to an indexed paired-end sequencing run of 2x151 cycles on an Illumina HiSeq 4000 system (Illumina, San Diego, CA, USA) (300 samples/lane). Single Cell RNA-Seq Illumina HiSeq 4000 gds 303874939 GSM3874939 GEO Accession GSM3874939