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1
+ 7 none fig 12.29x5.70 in Experimental overview
2
+ 8 none fig 12.45x5.67 in Pretraining data: 33.14 million training cells
3
+ 9 none fig 12.45x5.67 in Full source corpus: training, validation and test
4
+ 10 none fig 12.45x5.67 in From 41.40M source cells to 33.14M training cells
5
+ 11 none fig 12.45x5.67 in Recipe K and training exposure are different counts
6
+ 12 below fig 12.38x5.33 in Corpus scale and generation workflow
7
+ 13 none fig 12.45x4.07 in From Gaussian noise to generated cell states
8
+ 16 none fig 12.45x5.67 in Where context width and trunk width change
9
+ 17 none fig 12.45x5.67 in Predicted and oracle hints: one trained denoiser
10
+ 18 none fig 12.45x5.67 in Architecture: full and late validation progression
11
+ 19 below fig 9.57x4.63 in Width & context ablation: benchmark
12
+ 20 none fig 12.45x5.67 in Architecture arms: dimensions and endpoints
13
+ 21 below fig 9.57x4.63 in Gene context: 2k / 3k / 6k / 15k
14
+ 22 none fig 12.45x5.67 in Gene panels: progression relative to each endpoint
15
+ 23 none fig 12.45x5.67 in Gene-panel arms: exact sizes and training provenance
16
+ 24 none fig 12.45x5.67 in All ablation arms: parameters and training time
17
+ 25 none fig 12.15x5.70 in Real-cell repeat: a sampling reference
18
+ 26 none fig 12.45x5.48 in Native-pseudobulk model comparisons
19
+ 29 none fig 11.76x5.70 in Bulk and pooled cells: different expression values
20
+ 30 none fig 12.45x5.19 in Paired calibration reduces same-donor expression error
21
+ 31 below fig 10.47x4.63 in Consequence: cells off-manifold
22
+ 32 none fig 12.33x5.70 in Adaptation recovers the observed cell mixture
23
+ 33 none fig 12.45x5.35 in Adaptation: mixture error and expression agreement
24
+ 34 none fig 12.15x5.70 in Healthy paired data: full FT and LoRA
25
+ 35 none fig 12.45x5.40 in Full FT and LoRA ranks: quality and parameters
26
+ 36 none fig 11.45x5.70 in What does “all pairs” actually mean?
27
+ 37 none fig 12.19x5.70 in Healthy pair budget: correlation in all cell types
28
+ 38 none fig 12.19x5.70 in Healthy pair budget: error in all cell types
29
+ 39 right fig 9.20x5.17 in Five pairs, no extra validation: LoRA vs scSemi
30
+ 40 none fig 12.17x5.70 in Composition: error and donor-level wins
31
+ 43 right fig 9.20x5.18 in Disease signals with five training donors
32
+ 44 right fig 9.20x4.80 in 5-fold CV: disease signal
33
+ 45 below fig 11.93x4.63 in Disease genes at every list length (CAT)
34
+ 46 below fig 10.54x4.63 in Cell-type deconvolution, same pairs: disease signal
35
+ 47 none fig 12.45x5.70 in Disease gene rankings: complete CV comparison
36
+ 48 none fig 11.99x5.70 in Disease integrity depends on cohort and endpoint
37
+ 49 none fig 12.19x5.70 in Five-pair Sepsis: metrics across all support draws
38
+ 52 none fig 12.33x5.70 in Figure 5 targets begin with the source paper
39
+ 53 none fig 12.18x5.70 in Ye sepsis: published markers in paired scRNA
40
+ 54 none fig 12.33x5.70 in Transcriptional programs and rare-population identity
41
+ 60 none fig 12.45x2.62 in Corpus reference: assay and source composition
42
+ 61 below fig 12.45x4.61 in Backbone: SDD → PBISC-Diffusion
43
+ 62 below fig 12.45x4.61 in Bulk conditioning
44
+ 63 below fig 11.68x5.33 in Denoiser: joint value + support diffusion
45
+ 64 below fig 12.45x4.71 in Fine-tuning with paired bulk + sc
46
+ 65 below fig 12.35x4.63 in Evaluation design
47
+ 66 below fig 11.19x4.63 in How we score generated cells
48
+ 67 none fig 12.45x5.31 in Does the model follow its bulk conditioning?
49
+ 68 below fig 10.30x4.63 in SLE benchmark: PBISC vs scSemiProfiler
50
+ 69 below fig 10.79x4.63 in SLE benchmark: per cell type
51
+ 70 none fig 12.45x5.38 in Disjoint-cell controls test the bulk-broadcast baseline
52
+ 71 none fig 12.45x5.60 in SLE: what is added beyond the bulk broadcast?
53
+ 72 below fig 12.45x5.24 in Same shift in three paired cohorts
54
+ 73 none fig 12.45x5.64 in Input corrections on one real-reference UMAP
55
+ 74 none fig 12.45x4.86 in Where generated-cell density differs from real cells
56
+ 75 none fig 12.45x4.89 in Input calibration changes cell-type composition
57
+ 76 none fig 12.45x5.63 in Same noise, different input: matched-cell shifts
58
+ 77 none fig 12.45x4.77 in Matched noise separates cell state from cell identity
59
+ 78 none fig 12.45x5.63 in Input changes can switch the generated cell label
60
+ 79 none fig 12.45x5.58 in Nearest real cells: distance and label agreement
61
+ 80 none fig 12.34x5.70 in Composition agreement does not ensure state agreement
62
+ 81 none fig 12.45x5.47 in Gene-length effects in the bulk input
63
+ 82 none fig 12.45x5.47 in Gene-length effects within label-stable cells
64
+ 83 none fig 12.45x5.41 in Raw and TPM shifts persist within cell labels
65
+ 84 none fig 12.40x5.70 in Reference calibration leaves specific gene-state shifts
66
+ 85 none fig 12.45x5.45 in Donor trait axes and donor identification differ
67
+ 86 none fig 12.45x4.61 in Reference choice changes different quality endpoints
68
+ 88 none fig 12.45x4.72 in Technical repeats and follow-up are different controls
69
+ 89 none fig 12.45x5.32 in Annotation agreement and difficult categories
70
+ 90 none fig 12.45x5.40 in Depth matching changes precision and coverage
71
+ 91 none fig 12.45x4.86 in Detection and library size are separate diagnostics
72
+ 92 right fig 9.20x5.18 in Healthy cohort: LoRA cells cover the real ones
73
+ 93 right fig 9.20x4.79 in Healthy cohort: realism beyond precision/coverage
74
+ 94 right fig 9.20x5.14 in Healthy cohort: full vs LoRA vs condition encoder
75
+ 95 below fig 9.37x4.63 in Representative-dependent composition
76
+ 96 below fig 11.39x4.63 in Full vs LoRA vs cond.-encoder-only
77
+ 97 none fig 9.32x5.70 in Pair-budget summary: composition, coverage and steps
78
+ 98 right fig 9.20x5.09 in Healthy cohort: LoRA rank and K
79
+ 99 right fig 9.20x5.09 in Healthy paired-data learning curves
80
+ 100 right fig 9.20x4.66 in Time: days for scSemiProfiler, minutes for LoRA
81
+ 101 below fig 10.77x4.63 in 5 donors: time to apply
82
+ 102 below fig 9.99x4.63 in Pairs needed: composition, coverage, training steps
83
+ 103 below fig 10.08x4.63 in LoRA rank: r = 4, 16, 64
84
+ 104 right fig 8.31x5.70 in K diversification: no gain
85
+ 105 below fig 12.45x3.82 in Five paired cohorts
86
+ 106 none fig 12.45x4.70 in Sepsis: exact-five reconstruction across five draws
87
+ 107 none fig 12.45x5.18 in Sepsis: realism beyond precision and coverage
88
+ 108 none fig 12.45x4.70 in Imperial: first completed exact-five comparison
89
+ 109 below fig 10.01x4.63 in 5 donors: LoRA vs scSemiProfiler — cells
90
+ 110 below fig 10.04x4.63 in 5 donors: realism beyond precision/coverage
91
+ 111 below fig 10.02x4.63 in 5 donors: precision/coverage at k = 3, 5, 10
92
+ 112 below fig 10.09x4.63 in 5-fold: realism beyond precision/coverage
93
+ 113 below fig 11.74x4.63 in Same training pairs: LoRA vs scSemiProfiler
94
+ 114 below fig 11.85x4.63 in scSemiProfiler and the representative-copy baseline
95
+ 115 none fig 10.46x5.70 in Sepsis: patient-aware disease-gene agreement
96
+ 116 none fig 10.46x5.70 in Imperial: patient-aware disease-gene agreement
97
+ 117 below fig 10.60x4.63 in Sepsis: fine-tuning variants
98
+ 118 right fig 8.44x5.70 in Pairs needed: donor and disease signal
99
+ 119 below fig 10.53x4.63 in Cell-type deconvolution, same pairs: composition
100
+ 120 none fig 12.45x4.95 in Deconvolution: expression coverage limits the comparison
101
+ 121 none fig 12.45x5.08 in K=4,000 recipe: paired reconstruction quality
102
+ 122 none fig 12.45x5.08 in K=4,000 recipe: disease signal does not improve uniformly
103
+ 123 none fig 12.45x5.22 in K=4,000 recipe: calibration gains are selective
104
+ 124 none fig 12.45x4.66 in Influenza: response order versus response genes
105
+ 125 none fig 10.30x5.70 in COVID: calibration on a shared real-cell map
106
+ 126 none fig 10.82x5.70 in COVID monocytes: direction after depth matching
107
+ 127 none fig 11.44x5.70 in COVID monocytes: direction, magnitude and null
108
+ 128 none fig 11.44x5.70 in COVID CD14 monocytes: direction, magnitude and null
109
+ 129 none fig 12.45x5.02 in COVID: biological endpoints give a mixed verdict
110
+ 130 none fig 11.83x5.70 in Rare-state frequencies in observed cells
111
+ 131 none fig 11.35x5.70 in Rare-state misses: rules 1–8
112
+ 132 none fig 11.72x5.70 in Rare-state misses: rules 9–15
113
+ 133 none fig 12.06x5.70 in Rare-state fidelity: zero-aware reanalysis
114
+ 134 none fig 10.76x5.70 in Sepsis rare states across paired-data budgets
115
+ 135 none fig 12.45x5.62 in Sepsis rare-state direction across support budgets
116
+ 136 none fig 11.35x5.70 in Rare-state screen in DRESS, Kawasaki and SLE
117
+ 137 right fig 7.24x5.70 in Consequence: disease direction flips
118
+ 138 none fig 12.45x5.18 in C1Q: single-gene detection versus co-detection
119
+ 139 none fig 12.45x4.54 in Behçet: K=4,000 changes direction more than identity
120
+ 140 none fig 12.45x5.59 in Behcet: one-gene and multi-gene C1Q rules
121
+ 141 below fig 9.46x4.63 in Pairs from other cohorts do not transfer
122
+ 142 below fig 9.44x4.63 in Longer training on other cohorts: gap stays
123
+ 143 below fig 10.61x4.63 in No pretraining: same cohort, from scratch
124
+ 144 below fig 10.53x4.63 in No pretraining: other cohorts, from scratch
125
+ 145 below fig 10.20x4.63 in Rare states: from scratch vs pretrained
126
+ 146 below fig 10.12x4.63 in Appendix: scSemiProfiler without output threshold
127
+ 147 none fig 12.45x5.28 in Bulk-only exploration: calibration populations differ
128
+ 149 right fig 9.20x5.19 in Rare-state fractions: original analysis
129
+ 150 right fig 9.20x5.01 in Rare-state ranking: original analysis
130
+ 151 below fig 9.23x4.98 in Rare states: original five-fold analysis
131
+ 152 right fig 8.01x5.70 in Bulk-only cohort plan: original snapshot
132
+ 153 none fig 12.45x4.73 in Historical bulk-only search: no confirmed new finding
133
+ 155 below fig 12.45x4.62 in Next: other tissues from a few dozen pairs
134
+ {"slides": 155, "overview": 7, "training_corpus": 8, "full_source_support": 9, "source_bindings": 996}
135
+ convert /home/sj_server_1/PBISC/immun-pbmc-fm/model_8_sparse_data_diffusion/presentations/2026-09-30--paper-summary--r00/PBISC-Diffusion_expanded_master_20261014_figure1.pptx as a Impress document -> /home/sj_server_1/PBISC/immun-pbmc-fm/model_8_sparse_data_diffusion/presentations/2026-09-30--paper-summary--r00/PBISC-Diffusion_expanded_master_20261014_figure1.pdf using filter : impress_pdf_Export:{"UseTaggedPDF":{"type":"boolean","value":"false"},"PDFUACompliance":{"type":"boolean","value":"false"}}
136
+ {"pass": true, "counts": {"spec": 155, "pptx": 155, "pdf": 155}, "failures": []}
137
+ 7 none fig 12.29x5.70 in Experimental overview
138
+ 8 none fig 12.45x5.67 in Pretraining data: 33.14 million training cells
139
+ 9 none fig 12.45x5.67 in Full source corpus: training, validation and test
140
+ 10 none fig 12.45x5.67 in From 41.40M source cells to 33.14M training cells
141
+ 11 none fig 12.45x5.67 in Recipe K and training exposure are different counts
142
+ 12 below fig 12.38x5.33 in Corpus scale and generation workflow
143
+ 13 none fig 12.45x4.07 in From Gaussian noise to generated cell states
144
+ 16 none fig 12.45x5.67 in Where context width and trunk width change
145
+ 17 none fig 12.45x5.67 in Predicted and oracle hints: one trained denoiser
146
+ 18 none fig 12.45x5.67 in Architecture: full and late validation progression
147
+ 19 below fig 9.57x4.63 in Width & context ablation: benchmark
148
+ 20 none fig 12.45x5.67 in Architecture arms: dimensions and endpoints
149
+ 21 below fig 9.57x4.63 in Gene context: 2k / 3k / 6k / 15k
150
+ 22 none fig 12.45x5.67 in Gene panels: progression relative to each endpoint
151
+ 23 none fig 12.45x5.67 in Gene-panel arms: exact sizes and training provenance
152
+ 24 none fig 12.45x5.67 in All ablation arms: parameters and training time
153
+ 25 none fig 12.15x5.70 in Real-cell repeat: a sampling reference
154
+ 26 none fig 12.45x5.48 in Native-pseudobulk model comparisons
155
+ 29 none fig 11.76x5.70 in Bulk and pooled cells: different expression values
156
+ 30 none fig 12.45x5.19 in Paired calibration reduces same-donor expression error
157
+ 31 below fig 10.47x4.63 in Consequence: cells off-manifold
158
+ 32 none fig 12.33x5.70 in Adaptation recovers the observed cell mixture
159
+ 33 none fig 12.45x5.35 in Adaptation: mixture error and expression agreement
160
+ 34 none fig 12.15x5.70 in Healthy paired data: full FT and LoRA
161
+ 35 none fig 12.45x5.40 in Full FT and LoRA ranks: quality and parameters
162
+ 36 none fig 11.45x5.70 in What does “all pairs” actually mean?
163
+ 37 none fig 12.19x5.70 in Healthy pair budget: correlation in all cell types
164
+ 38 none fig 12.19x5.70 in Healthy pair budget: error in all cell types
165
+ 39 right fig 9.20x5.17 in Five pairs, no extra validation: LoRA vs scSemi
166
+ 40 none fig 12.17x5.70 in Composition: error and donor-level wins
167
+ 43 right fig 9.20x5.18 in Disease signals with five training donors
168
+ 44 right fig 9.20x4.80 in 5-fold CV: disease signal
169
+ 45 below fig 11.93x4.63 in Disease genes at every list length (CAT)
170
+ 46 below fig 10.54x4.63 in Cell-type deconvolution, same pairs: disease signal
171
+ 47 none fig 12.45x5.70 in Disease gene rankings: complete CV comparison
172
+ 48 none fig 11.99x5.70 in Disease integrity depends on cohort and endpoint
173
+ 49 none fig 12.19x5.70 in Five-pair Sepsis: metrics across all support draws
174
+ 52 none fig 12.33x5.70 in Figure 5 targets begin with the source paper
175
+ 53 none fig 12.18x5.70 in Ye sepsis: published markers in paired scRNA
176
+ 54 none fig 12.33x5.70 in Transcriptional programs and rare-population identity
177
+ 60 none fig 12.45x2.62 in Corpus reference: assay and source composition
178
+ 61 below fig 12.45x4.61 in Backbone: SDD → PBISC-Diffusion
179
+ 62 below fig 12.45x4.61 in Bulk conditioning
180
+ 63 below fig 11.68x5.33 in Denoiser: joint value + support diffusion
181
+ 64 below fig 12.45x4.71 in Fine-tuning with paired bulk + sc
182
+ 65 below fig 12.35x4.63 in Evaluation design
183
+ 66 below fig 11.19x4.63 in How we score generated cells
184
+ 67 none fig 12.45x5.31 in Does the model follow its bulk conditioning?
185
+ 68 below fig 10.30x4.63 in SLE benchmark: PBISC vs scSemiProfiler
186
+ 69 below fig 10.79x4.63 in SLE benchmark: per cell type
187
+ 70 none fig 12.45x5.38 in Disjoint-cell controls test the bulk-broadcast baseline
188
+ 71 none fig 12.45x5.60 in SLE: what is added beyond the bulk broadcast?
189
+ 72 below fig 12.45x5.24 in Same shift in three paired cohorts
190
+ 73 none fig 12.45x5.64 in Input corrections on one real-reference UMAP
191
+ 74 none fig 12.45x4.86 in Where generated-cell density differs from real cells
192
+ 75 none fig 12.45x4.89 in Input calibration changes cell-type composition
193
+ 76 none fig 12.45x5.63 in Same noise, different input: matched-cell shifts
194
+ 77 none fig 12.45x4.77 in Matched noise separates cell state from cell identity
195
+ 78 none fig 12.45x5.63 in Input changes can switch the generated cell label
196
+ 79 none fig 12.45x5.58 in Nearest real cells: distance and label agreement
197
+ 80 none fig 12.34x5.70 in Composition agreement does not ensure state agreement
198
+ 81 none fig 12.45x5.47 in Gene-length effects in the bulk input
199
+ 82 none fig 12.45x5.47 in Gene-length effects within label-stable cells
200
+ 83 none fig 12.45x5.41 in Raw and TPM shifts persist within cell labels
201
+ 84 none fig 12.40x5.70 in Reference calibration leaves specific gene-state shifts
202
+ 85 none fig 12.45x5.45 in Donor trait axes and donor identification differ
203
+ 86 none fig 12.45x4.61 in Reference choice changes different quality endpoints
204
+ 88 none fig 12.45x4.72 in Technical repeats and follow-up are different controls
205
+ 89 none fig 12.45x5.32 in Annotation agreement and difficult categories
206
+ 90 none fig 12.45x5.40 in Depth matching changes precision and coverage
207
+ 91 none fig 12.45x4.86 in Detection and library size are separate diagnostics
208
+ 92 right fig 9.20x5.18 in Healthy cohort: LoRA cells cover the real ones
209
+ 93 right fig 9.20x4.79 in Healthy cohort: realism beyond precision/coverage
210
+ 94 right fig 9.20x5.14 in Healthy cohort: full vs LoRA vs condition encoder
211
+ 95 below fig 9.37x4.63 in Representative-dependent composition
212
+ 96 below fig 11.39x4.63 in Full vs LoRA vs cond.-encoder-only
213
+ 97 none fig 9.32x5.70 in Pair-budget summary: composition, coverage and steps
214
+ 98 right fig 9.20x5.09 in Healthy cohort: LoRA rank and K
215
+ 99 right fig 9.20x5.09 in Healthy paired-data learning curves
216
+ 100 right fig 9.20x4.66 in Time: days for scSemiProfiler, minutes for LoRA
217
+ 101 below fig 10.77x4.63 in 5 donors: time to apply
218
+ 102 below fig 9.99x4.63 in Pairs needed: composition, coverage, training steps
219
+ 103 below fig 10.08x4.63 in LoRA rank: r = 4, 16, 64
220
+ 104 right fig 8.31x5.70 in K diversification: no gain
221
+ 105 below fig 12.45x3.82 in Five paired cohorts
222
+ 106 none fig 12.45x4.70 in Sepsis: exact-five reconstruction across five draws
223
+ 107 none fig 12.45x5.18 in Sepsis: realism beyond precision and coverage
224
+ 108 none fig 12.45x4.70 in Imperial: first completed exact-five comparison
225
+ 109 below fig 10.01x4.63 in 5 donors: LoRA vs scSemiProfiler — cells
226
+ 110 below fig 10.04x4.63 in 5 donors: realism beyond precision/coverage
227
+ 111 below fig 10.02x4.63 in 5 donors: precision/coverage at k = 3, 5, 10
228
+ 112 below fig 10.09x4.63 in 5-fold: realism beyond precision/coverage
229
+ 113 below fig 11.74x4.63 in Same training pairs: LoRA vs scSemiProfiler
230
+ 114 below fig 11.85x4.63 in scSemiProfiler and the representative-copy baseline
231
+ 115 none fig 10.46x5.70 in Sepsis: patient-aware disease-gene agreement
232
+ 116 none fig 10.46x5.70 in Imperial: patient-aware disease-gene agreement
233
+ 117 below fig 10.60x4.63 in Sepsis: fine-tuning variants
234
+ 118 right fig 8.44x5.70 in Pairs needed: donor and disease signal
235
+ 119 below fig 10.53x4.63 in Cell-type deconvolution, same pairs: composition
236
+ 120 none fig 12.45x4.95 in Deconvolution: expression coverage limits the comparison
237
+ 121 none fig 12.45x5.08 in K=4,000 recipe: paired reconstruction quality
238
+ 122 none fig 12.45x5.08 in K=4,000 recipe: disease signal does not improve uniformly
239
+ 123 none fig 12.45x5.22 in K=4,000 recipe: calibration gains are selective
240
+ 124 none fig 12.45x4.66 in Influenza: response order versus response genes
241
+ 125 none fig 10.30x5.70 in COVID: calibration on a shared real-cell map
242
+ 126 none fig 10.82x5.70 in COVID monocytes: direction after depth matching
243
+ 127 none fig 11.44x5.70 in COVID monocytes: direction, magnitude and null
244
+ 128 none fig 11.44x5.70 in COVID CD14 monocytes: direction, magnitude and null
245
+ 129 none fig 12.45x5.02 in COVID: biological endpoints give a mixed verdict
246
+ 130 none fig 11.83x5.70 in Rare-state frequencies in observed cells
247
+ 131 none fig 11.35x5.70 in Rare-state misses: rules 1–8
248
+ 132 none fig 11.72x5.70 in Rare-state misses: rules 9–15
249
+ 133 none fig 12.06x5.70 in Rare-state fidelity: zero-aware reanalysis
250
+ 134 none fig 10.76x5.70 in Sepsis rare states across paired-data budgets
251
+ 135 none fig 12.45x5.62 in Sepsis rare-state direction across support budgets
252
+ 136 none fig 11.35x5.70 in Rare-state screen in DRESS, Kawasaki and SLE
253
+ 137 right fig 7.24x5.70 in Consequence: disease direction flips
254
+ 138 none fig 12.45x5.18 in C1Q: single-gene detection versus co-detection
255
+ 139 none fig 12.45x4.54 in Behçet: K=4,000 changes direction more than identity
256
+ 140 none fig 12.45x5.59 in Behcet: one-gene and multi-gene C1Q rules
257
+ 141 below fig 9.46x4.63 in Pairs from other cohorts do not transfer
258
+ 142 below fig 9.44x4.63 in Longer training on other cohorts: gap stays
259
+ 143 below fig 10.61x4.63 in No pretraining: same cohort, from scratch
260
+ 144 below fig 10.53x4.63 in No pretraining: other cohorts, from scratch
261
+ 145 below fig 10.20x4.63 in Rare states: from scratch vs pretrained
262
+ 146 below fig 10.12x4.63 in Appendix: scSemiProfiler without output threshold
263
+ 147 none fig 12.45x5.28 in Bulk-only exploration: calibration populations differ
264
+ 149 right fig 9.20x5.19 in Rare-state fractions: original analysis
265
+ 150 right fig 9.20x5.01 in Rare-state ranking: original analysis
266
+ 151 below fig 9.23x4.98 in Rare states: original five-fold analysis
267
+ 152 right fig 8.01x5.70 in Bulk-only cohort plan: original snapshot
268
+ 153 none fig 12.45x4.73 in Historical bulk-only search: no confirmed new finding
269
+ 155 below fig 12.45x4.62 in Next: other tissues from a few dozen pairs
270
+ {"slides": 155, "overview": 7, "training_corpus": 8, "full_source_support": 9, "source_bindings": 996}
271
+ convert /home/sj_server_1/PBISC/immun-pbmc-fm/model_8_sparse_data_diffusion/presentations/2026-09-30--paper-summary--r00/PBISC-Diffusion_expanded_master_20261014_figure1.pptx as a Impress document -> /home/sj_server_1/PBISC/immun-pbmc-fm/model_8_sparse_data_diffusion/presentations/2026-09-30--paper-summary--r00/PBISC-Diffusion_expanded_master_20261014_figure1.pdf using filter : impress_pdf_Export:{"UseTaggedPDF":{"type":"boolean","value":"false"},"PDFUACompliance":{"type":"boolean","value":"false"}}
272
+ Overwriting: /home/sj_server_1/PBISC/immun-pbmc-fm/model_8_sparse_data_diffusion/presentations/2026-09-30--paper-summary--r00/PBISC-Diffusion_expanded_master_20261014_figure1.pdf
273
+ {"pass": true, "counts": {"spec": 155, "pptx": 155, "pdf": 155}, "failures": []}