SRX22381255 GSM7882922_r1 SRP470358 PRJNA1036165 SRS19427815 GSM7882922 GSM7882922 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Tumor tissue was placed in a digestion buffer containing trypsin, DNase, and an enzymatic cocktail (Supplementary Table 7) and digested at 37°C for 42 minutes (37C_m_TDK_2 program) on a gentleMACS Octo Dissociator (Miltenyi Biotec, 130-096-427). Cell suspensions were then filtered through a 40 μm cell strainer (Corning, 431750) and red blood cells were removed by incubation with red cell lysis buffer (Millipore Sigma, 11814389001), before a final resuspension in 100 μL PBS + 0.01% BSA. Single Cell 3' v3, 10x Genomics NextSeq 500 SRX22381256 GSM7882923_r1 SRP470358 PRJNA1036165 SRS19427816 GSM7882923 GSM7882923 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Tumor tissue was placed in a digestion buffer containing trypsin, DNase, and an enzymatic cocktail (Supplementary Table 7) and digested at 37°C for 42 minutes (37C_m_TDK_2 program) on a gentleMACS Octo Dissociator (Miltenyi Biotec, 130-096-427). Cell suspensions were then filtered through a 40 μm cell strainer (Corning, 431750) and red blood cells were removed by incubation with red cell lysis buffer (Millipore Sigma, 11814389001), before a final resuspension in 100 μL PBS + 0.01% BSA. Single Cell 3' v3, 10x Genomics NextSeq 500 SRX22381257 GSM7882924_r1 SRP470358 PRJNA1036165 SRS19427817 GSM7882924 GSM7882924 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Tumor tissue was placed in a digestion buffer containing trypsin, DNase, and an enzymatic cocktail (Supplementary Table 7) and digested at 37°C for 42 minutes (37C_m_TDK_2 program) on a gentleMACS Octo Dissociator (Miltenyi Biotec, 130-096-427). Cell suspensions were then filtered through a 40 μm cell strainer (Corning, 431750) and red blood cells were removed by incubation with red cell lysis buffer (Millipore Sigma, 11814389001), before a final resuspension in 100 μL PBS + 0.01% BSA. Single Cell 3' v3, 10x Genomics NextSeq 500 SRX22381258 GSM7882925_r1 SRP470358 PRJNA1036165 SRS19427818 GSM7882925 GSM7882925 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Tumor tissue was placed in a digestion buffer containing trypsin, DNase, and an enzymatic cocktail (Supplementary Table 7) and digested at 37°C for 42 minutes (37C_m_TDK_2 program) on a gentleMACS Octo Dissociator (Miltenyi Biotec, 130-096-427). Cell suspensions were then filtered through a 40 μm cell strainer (Corning, 431750) and red blood cells were removed by incubation with red cell lysis buffer (Millipore Sigma, 11814389001), before a final resuspension in 100 μL PBS + 0.01% BSA. Single Cell 3' v3, 10x Genomics NextSeq 500 SRX22381259 GSM7882926_r1 SRP470358 PRJNA1036165 SRS19427819 GSM7882926 GSM7882926 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Tumor tissue was placed in a digestion buffer containing trypsin, DNase, and an enzymatic cocktail (Supplementary Table 7) and digested at 37°C for 42 minutes (37C_m_TDK_2 program) on a gentleMACS Octo Dissociator (Miltenyi Biotec, 130-096-427). Cell suspensions were then filtered through a 40 μm cell strainer (Corning, 431750) and red blood cells were removed by incubation with red cell lysis buffer (Millipore Sigma, 11814389001), before a final resuspension in 100 μL PBS + 0.01% BSA. Single Cell 3' v3, 10x Genomics NextSeq 500 SRX22381260 GSM7882927_r1 SRP470358 PRJNA1036165 SRS19427821 GSM7882927 GSM7882927 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA Tumor tissue was placed in a digestion buffer containing trypsin, DNase, and an enzymatic cocktail (Supplementary Table 7) and digested at 37°C for 42 minutes (37C_m_TDK_2 program) on a gentleMACS Octo Dissociator (Miltenyi Biotec, 130-096-427). Cell suspensions were then filtered through a 40 μm cell strainer (Corning, 431750) and red blood cells were removed by incubation with red cell lysis buffer (Millipore Sigma, 11814389001), before a final resuspension in 100 μL PBS + 0.01% BSA. Single Cell 3' v3, 10x Genomics NextSeq 500