Clustering data with hclust algorithm for (Study ST002125)

(Analysis AN003478)
MetaboliteStructureF1F2F3F4F5F6F7F8F9F10F11F12F13F14
[13C]FumatateME516688NANA4.390.010.010.014.600.010.010.010.010.020.022.90
[13C]Alpha_KetoglutarateME516686NANA4.460.010.010.014.430.010.010.010.020.050.032.93
[13C]SuccinateME516690NANA4.500.010.010.014.490.010.010.010.010.020.012.91
[13C]CitrateME516687NANA4.440.010.010.014.930.010.010.010.020.060.042.45
[13C]MalateME516689NANA4.760.010.020.024.920.010.020.010.020.030.022.18
[13C, 15N]Glutamic acid, 3TBDMSME516673NANA0.032.870.901.530.032.370.671.261.090.220.640.01
[13C, 15N]Alanine, 2TBDMSME516671NANA0.011.491.361.230.011.411.361.231.471.091.270.01
[13C, 15N]Leucine, 2TBDMSME516677NANA0.022.150.931.490.022.110.841.481.360.470.900.01
[13C, 15N]Tyrosine, 3TBDMSME516684NANA0.022.141.021.590.022.010.821.561.250.560.840.01
[13C, 15N]Proline, 2TBDMSME516681NANA0.021.921.181.540.022.121.081.701.130.360.780.01
[13C, 15N]Isoleucine, 2TBDMSME516676NANA0.021.901.161.620.021.791.401.611.270.400.740.01
[13C, 15N]Histidine, 3TBDMSME516675NANA0.021.871.371.580.021.771.251.491.270.370.880.02
[13C, 15N]Valine, 2TBDMSME516685NANA0.001.841.261.590.001.871.151.531.350.460.830.00
[13C, 15N]Aspartic acid, 3TBDMSME516672NANA0.022.200.901.210.021.960.871.041.740.671.060.02
[13C, 15N]Methionine, 2TBDMSME516679NANA0.021.921.291.540.021.641.161.321.330.750.900.01
[13C, 15N]Glycine, 2TBDMSME516674NANA0.021.771.131.380.021.731.221.301.480.741.060.02
[13C, 15N]Serine, 3TBDMSME516682NANA0.021.761.101.390.021.811.071.481.270.901.070.01
[13C, 15N]Lysine, 3TBDMSME516678NANA0.021.900.931.330.021.830.931.191.570.771.290.01
[13C, 15N]Phenylalanine, 2TBDMSME516680NANA0.021.840.871.340.021.750.971.501.780.681.130.02
[13C, 15N]Threonine, 3TBDMSME516683NANA0.021.731.001.380.021.701.071.491.640.791.080.01

Factors:

F1Source_Name[gating]:Bone marrow supernatant | Treatment:5 FU 2 weeks | Batch:1c | Note:Unlabeled AAs were used for total AA (FigS2.D)
F2Source_Name[gating]:Bone marrow supernatant | Treatment:HSC Basal | Batch:1c | Note:Unlabeled AAs were used for total AA (FigS2.D)
F3Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:5 FU 2 weeks, [13C, 15N] AAs were incorporated for 1 h | Batch:1c | Note:[13C, 15N] AAs were used for AA uptake (Fig2.B, Fig5M); unlabeled AAs and TCA substrate were used for total AA levels (Fig2.C, Fig5K) and TCA substrate levels (Fig2.K, Fig5J).
F4Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:5 FU 2 weeks, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 0 h | Batch:1b | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig2.D).
F5Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:5 FU 2 weeks, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 12 h | Batch:1b | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig2.D).
F6Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:5 FU 2 weeks, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 6 h | Batch:1b | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig2.D).
F7Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ex vivo culture 2 weeks, [13C, 15N] AAs were incorporated for 1 h | Batch:1c | Note:[13C, 15N] AAs were used for AA uptake (Fig2.B); unlabeled AAs and TCA substrate were used for total AA levels (Fig2.C) and TCA substrate levels (Fig2.K).
F8Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ex vivo culture 2 weeks, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 0 h | Batch:1b | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig2.D).
F9Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ex vivo culture 2 weeks, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 12 h | Batch:1b | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig2.D).
F10Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:Ex vivo culture 2 weeks, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 6 h | Batch:1b | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig2.D).
F11Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:HSC Basal, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 0 h | Batch:1b | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig1.C, Fig2.D).
F12Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:HSC Basal, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 12 h | Batch:1b | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig1.C, Fig2.D).
F13Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:HSC Basal, [13C, 15N] AAs were incorporated for 24 h and subsequently washed out for 6 h | Batch:1b | Note:[13C, 15N] AA levels and [13C]TCA substrate levels in different time point were calculated for AA catabolism (Fig1.C, Fig2.D).
F14Source_Name[gating]:Lin– Scal1+ c-Kit+ CD48– CD150+ (HSC) | Treatment:HSC Basal or Ctrl, [13C, 15N] AAs were incorporated for 1 h | Batch:1c | Note:[13C, 15N] AAs were used for AA uptake (Fig2.B, Fig5M); unlabeled AAs and TCA substrate were used for total AA levels (Fig2.C, Fig5K) and TCA substrate levels (Fig2.K, Fig5J).
Data matrix
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