SRX2973707 CT_R3 SRP110808 bp0 Mentha piperita plants of 45 days post-germination were treated or not with salycilic acid (SA) 2 mM by foliar applications. These plants were used in the differential gene expression evaluated. Plants of one week after foliar SA applications were used to extract total RNA from young leaves using TRIzol ® reagent (Invitrogen Carlsbad, CA, USA) and purified using RNeasy kit (Qiagen). The contaminating genomic DNA was removed using Dnase I, and RNA was quantified using a Nanodrop 2000 (Thermo Fisher scientific). Three replicates of cDNA libraries were prepared, clustered and sequenced usingthe technology HiSeq 2000 (Illumina) was carried out at LANGEBIO (Irapuato,Mexico). SRS2328685 Control_R3 CT_R3 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX2973708 CT_R4 SRP110808 bp0 Mentha piperita plants of 45 days post-germination were treated or not with salycilic acid (SA) 2 mM by foliar applications. These plants were used in the differential gene expression evaluated. Plants of one week after foliar SA applications were used to extract total RNA from young leaves using TRIzol ® reagent (Invitrogen Carlsbad, CA, USA) and purified using RNeasy kit (Qiagen). The contaminating genomic DNA was removed using Dnase I, and RNA was quantified using a Nanodrop 2000 (Thermo Fisher scientific). Three replicates of cDNA libraries were prepared, clustered and sequenced usingthe technology HiSeq 2000 (Illumina) was carried out at LANGEBIO (Irapuato,Mexico). SRS2328686 Control_R4 CT_R4 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX2973709 CT_R1 SRP110808 bp0 Mentha piperita plants of 45 days post-germination were treated or not with salycilic acid (SA) 2 mM by foliar applications. These plants were used in the differential gene expression evaluated. Plants of one week after foliar SA applications were used to extract total RNA from young leaves using TRIzol ® reagent (Invitrogen Carlsbad, CA, USA) and purified using RNeasy kit (Qiagen). The contaminating genomic DNA was removed using Dnase I, and RNA was quantified using a Nanodrop 2000 (Thermo Fisher scientific). Three replicates of cDNA libraries were prepared, clustered and sequenced usingthe technology HiSeq 2000 (Illumina) was carried out at LANGEBIO (Irapuato,Mexico). SRS2328687 Control_R1 CT_R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX2973710 CT_R2 SRP110808 bp0 Mentha piperita plants of 45 days post-germination were treated or not with salycilic acid (SA) 2 mM by foliar applications. These plants were used in the differential gene expression evaluated. Plants of one week after foliar SA applications were used to extract total RNA from young leaves using TRIzol ® reagent (Invitrogen Carlsbad, CA, USA) and purified using RNeasy kit (Qiagen). The contaminating genomic DNA was removed using Dnase I, and RNA was quantified using a Nanodrop 2000 (Thermo Fisher scientific). Three replicates of cDNA libraries were prepared, clustered and sequenced usingthe technology HiSeq 2000 (Illumina) was carried out at LANGEBIO (Irapuato,Mexico). SRS2328688 Control_R2 CT_R2 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX2973711 SA_R1 SRP110808 bp0 Mentha piperita plants of 45 days post-germination were treated or not with salycilic acid (SA) 2 mM by foliar applications. These plants were used in the differential gene expression evaluated. Plants of one week after foliar SA applications were used to extract total RNA from young leaves using TRIzol ® reagent (Invitrogen Carlsbad, CA, USA) and purified using RNeasy kit (Qiagen). The contaminating genomic DNA was removed using Dnase I, and RNA was quantified using a Nanodrop 2000 (Thermo Fisher scientific). Three replicates of cDNA libraries were prepared, clustered and sequenced usingthe technology HiSeq 2000 (Illumina) was carried out at LANGEBIO (Irapuato,Mexico). SRS2328693 SA_R1 SA_R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX2973712 SA_R2 SRP110808 bp0 Mentha piperita plants of 45 days post-germination were treated or not with salycilic acid (SA) 2 mM by foliar applications. These plants were used in the differential gene expression evaluated. Plants of one week after foliar SA applications were used to extract total RNA from young leaves using TRIzol ® reagent (Invitrogen Carlsbad, CA, USA) and purified using RNeasy kit (Qiagen). The contaminating genomic DNA was removed using Dnase I, and RNA was quantified using a Nanodrop 2000 (Thermo Fisher scientific). Three replicates of cDNA libraries were prepared, clustered and sequenced usingthe technology HiSeq 2000 (Illumina) was carried out at LANGEBIO (Irapuato,Mexico). SRS2328689 SA_R2 SA_R2 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX2973713 CT_R5 SRP110808 bp0 Mentha piperita plants of 45 days post-germination were treated or not with salycilic acid (SA) 2 mM by foliar applications. These plants were used in the differential gene expression evaluated. Plants of one week after foliar SA applications were used to extract total RNA from young leaves using TRIzol ® reagent (Invitrogen Carlsbad, CA, USA) and purified using RNeasy kit (Qiagen). The contaminating genomic DNA was removed using Dnase I, and RNA was quantified using a Nanodrop 2000 (Thermo Fisher scientific). Three replicates of cDNA libraries were prepared, clustered and sequenced usingthe technology HiSeq 2000 (Illumina) was carried out at LANGEBIO (Irapuato,Mexico). SRS2328690 Control_R5 CT_R5 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX2973714 CT_R6 SRP110808 bp0 Mentha piperita plants of 45 days post-germination were treated or not with salycilic acid (SA) 2 mM by foliar applications. These plants were used in the differential gene expression evaluated. Plants of one week after foliar SA applications were used to extract total RNA from young leaves using TRIzol ® reagent (Invitrogen Carlsbad, CA, USA) and purified using RNeasy kit (Qiagen). The contaminating genomic DNA was removed using Dnase I, and RNA was quantified using a Nanodrop 2000 (Thermo Fisher scientific). Three replicates of cDNA libraries were prepared, clustered and sequenced usingthe technology HiSeq 2000 (Illumina) was carried out at LANGEBIO (Irapuato,Mexico). SRS2328691 Control_R6 CT_R6 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX2973715 SA_R3 SRP110808 bp0 Mentha piperita plants of 45 days post-germination were treated or not with salycilic acid (SA) 2 mM by foliar applications. These plants were used in the differential gene expression evaluated. Plants of one week after foliar SA applications were used to extract total RNA from young leaves using TRIzol ® reagent (Invitrogen Carlsbad, CA, USA) and purified using RNeasy kit (Qiagen). The contaminating genomic DNA was removed using Dnase I, and RNA was quantified using a Nanodrop 2000 (Thermo Fisher scientific). Three replicates of cDNA libraries were prepared, clustered and sequenced usingthe technology HiSeq 2000 (Illumina) was carried out at LANGEBIO (Irapuato,Mexico). SRS2328692 SA_R3 SA_R3 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX2973716 SA_R4 SRP110808 bp0 Mentha piperita plants of 45 days post-germination were treated or not with salycilic acid (SA) 2 mM by foliar applications. These plants were used in the differential gene expression evaluated. Plants of one week after foliar SA applications were used to extract total RNA from young leaves using TRIzol ® reagent (Invitrogen Carlsbad, CA, USA) and purified using RNeasy kit (Qiagen). The contaminating genomic DNA was removed using Dnase I, and RNA was quantified using a Nanodrop 2000 (Thermo Fisher scientific). Three replicates of cDNA libraries were prepared, clustered and sequenced usingthe technology HiSeq 2000 (Illumina) was carried out at LANGEBIO (Irapuato,Mexico). SRS2328694 SA_R4 SA_R4 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX2973717 SA_R5 SRP110808 bp0 Mentha piperita plants of 45 days post-germination were treated or not with salycilic acid (SA) 2 mM by foliar applications. These plants were used in the differential gene expression evaluated. Plants of one week after foliar SA applications were used to extract total RNA from young leaves using TRIzol ® reagent (Invitrogen Carlsbad, CA, USA) and purified using RNeasy kit (Qiagen). The contaminating genomic DNA was removed using Dnase I, and RNA was quantified using a Nanodrop 2000 (Thermo Fisher scientific). Three replicates of cDNA libraries were prepared, clustered and sequenced usingthe technology HiSeq 2000 (Illumina) was carried out at LANGEBIO (Irapuato,Mexico). SRS2328699 SA_R5 SA_R5 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500 SRX2973718 SA_R6 SRP110808 bp0 Mentha piperita plants of 45 days post-germination were treated or not with salycilic acid (SA) 2 mM by foliar applications. These plants were used in the differential gene expression evaluated. Plants of one week after foliar SA applications were used to extract total RNA from young leaves using TRIzol ® reagent (Invitrogen Carlsbad, CA, USA) and purified using RNeasy kit (Qiagen). The contaminating genomic DNA was removed using Dnase I, and RNA was quantified using a Nanodrop 2000 (Thermo Fisher scientific). Three replicates of cDNA libraries were prepared, clustered and sequenced usingthe technology HiSeq 2000 (Illumina) was carried out at LANGEBIO (Irapuato,Mexico). SRS2328698 SA_R6 SA_R6 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 2500