Archive 4 checkpoints (1-4)
Browse files- paper-releases/pbisc-diffusion/updates/20261013T072655Z-enriched-140-slide-master/diffusion/dataset/server_1/model8/presentations/2026-09-30--paper-summary--r00/data/figure_enrichment_20261013/qa/contact11.png +3 -0
- paper-releases/pbisc-diffusion/updates/20261013T072655Z-enriched-140-slide-master/diffusion/dataset/server_1/model8/presentations/2026-09-30--paper-summary--r00/data/figure_enrichment_20261013/qa/contact12.png +3 -0
- paper-releases/pbisc-diffusion/updates/20261013T072655Z-enriched-140-slide-master/diffusion/dataset/server_1/model8/presentations/2026-09-30--paper-summary--r00/data/figure_enrichment_20261013/render.log +244 -0
- paper-releases/pbisc-diffusion/updates/20261013T072655Z-enriched-140-slide-master/diffusion/dataset/server_1/model8/presentations/2026-09-30--paper-summary--r00/data/figure_enrichment_20261013/render.py +27 -0
paper-releases/pbisc-diffusion/updates/20261013T072655Z-enriched-140-slide-master/diffusion/dataset/server_1/model8/presentations/2026-09-30--paper-summary--r00/data/figure_enrichment_20261013/qa/contact11.png
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Git LFS Details
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paper-releases/pbisc-diffusion/updates/20261013T072655Z-enriched-140-slide-master/diffusion/dataset/server_1/model8/presentations/2026-09-30--paper-summary--r00/data/figure_enrichment_20261013/qa/contact12.png
ADDED
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Git LFS Details
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paper-releases/pbisc-diffusion/updates/20261013T072655Z-enriched-140-slide-master/diffusion/dataset/server_1/model8/presentations/2026-09-30--paper-summary--r00/data/figure_enrichment_20261013/render.log
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| 1 |
+
7 right fig 9.20x4.86 in Experimental overview
|
| 2 |
+
8 below fig 12.45x2.62 in Pretraining corpus
|
| 3 |
+
9 below fig 12.38x5.33 in Corpus scale and generation workflow
|
| 4 |
+
10 none fig 12.45x4.07 in From Gaussian noise to generated cell states
|
| 5 |
+
13 none fig 12.45x5.67 in Where context width and trunk width change
|
| 6 |
+
14 none fig 12.45x5.67 in Predicted and oracle hints: one trained denoiser
|
| 7 |
+
15 none fig 12.45x5.67 in Architecture: full and late validation progression
|
| 8 |
+
16 below fig 9.57x4.63 in Width & context ablation: benchmark
|
| 9 |
+
17 none fig 12.45x5.67 in Architecture arms: dimensions and endpoints
|
| 10 |
+
18 below fig 9.57x4.63 in Gene context: 2k / 3k / 6k / 15k
|
| 11 |
+
19 none fig 12.45x5.67 in Gene panels: progression relative to each endpoint
|
| 12 |
+
20 none fig 12.45x5.67 in Gene-panel arms: exact sizes and training provenance
|
| 13 |
+
21 none fig 12.45x5.67 in All ablation arms: parameters and training time
|
| 14 |
+
22 none fig 12.15x5.70 in Real-cell repeat: a sampling reference
|
| 15 |
+
23 none fig 12.45x5.47 in Native-pseudobulk model comparisons
|
| 16 |
+
26 none fig 11.76x5.70 in Bulk and pooled cells: different expression values
|
| 17 |
+
27 none fig 12.45x5.18 in Paired calibration reduces same-donor expression error
|
| 18 |
+
28 below fig 10.47x4.63 in Consequence: cells off-manifold
|
| 19 |
+
29 none fig 12.15x5.70 in Healthy paired data: full FT and LoRA
|
| 20 |
+
30 none fig 12.45x5.40 in Full FT and LoRA ranks: quality and parameters
|
| 21 |
+
31 right fig 9.20x5.63 in Healthy paired-data budget: n training + 7 validation
|
| 22 |
+
32 right fig 9.20x5.17 in Five pairs, no extra validation: LoRA vs scSemi
|
| 23 |
+
33 none fig 12.17x5.70 in Composition: error and donor-level wins
|
| 24 |
+
36 right fig 9.20x5.18 in Disease signals with five training donors
|
| 25 |
+
37 right fig 9.20x4.80 in 5-fold CV: disease signal
|
| 26 |
+
38 below fig 11.93x4.63 in Disease genes at every list length (CAT)
|
| 27 |
+
39 below fig 10.54x4.63 in Cell-type deconvolution, same pairs: disease signal
|
| 28 |
+
47 below fig 12.45x4.61 in Backbone: SDD → PBISC-Diffusion
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| 29 |
+
48 below fig 12.45x4.61 in Bulk conditioning
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| 30 |
+
49 below fig 11.68x5.33 in Denoiser: joint value + support diffusion
|
| 31 |
+
50 below fig 12.45x4.71 in Fine-tuning with paired bulk + sc
|
| 32 |
+
51 below fig 12.35x4.63 in Evaluation design
|
| 33 |
+
52 below fig 11.19x4.63 in How we score generated cells
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| 34 |
+
53 none fig 12.45x5.31 in Does the model follow its bulk conditioning?
|
| 35 |
+
54 below fig 10.30x4.63 in SLE benchmark: PBISC vs scSemiProfiler
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| 36 |
+
55 below fig 10.79x4.63 in SLE benchmark: per cell type
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| 37 |
+
56 none fig 12.45x5.38 in Disjoint-cell controls test the bulk-broadcast baseline
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| 38 |
+
57 none fig 12.45x5.60 in SLE: what is added beyond the bulk broadcast?
|
| 39 |
+
58 below fig 12.45x5.24 in Same shift in three paired cohorts
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| 40 |
+
59 none fig 12.45x5.64 in Input corrections on one real-reference UMAP
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| 41 |
+
60 none fig 12.45x4.86 in Where generated-cell density differs from real cells
|
| 42 |
+
61 none fig 12.45x4.89 in Input calibration changes cell-type composition
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| 43 |
+
62 none fig 12.45x5.63 in Same noise, different input: matched-cell shifts
|
| 44 |
+
63 none fig 12.45x4.76 in Matched noise separates cell state from cell identity
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| 45 |
+
64 none fig 12.45x5.63 in Input changes can switch the generated cell label
|
| 46 |
+
65 none fig 12.45x5.58 in Nearest real cells: distance and label agreement
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| 47 |
+
66 none fig 12.45x5.52 in Composition agreement does not ensure state agreement
|
| 48 |
+
67 none fig 12.45x5.47 in Gene-length effects in the bulk input
|
| 49 |
+
68 none fig 12.45x5.47 in Gene-length effects within label-stable cells
|
| 50 |
+
69 none fig 12.45x5.41 in Raw and TPM shifts persist within cell labels
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| 51 |
+
70 none fig 12.40x5.70 in Reference calibration leaves specific gene-state shifts
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| 52 |
+
71 none fig 12.45x5.45 in Donor trait axes and donor identification differ
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| 53 |
+
72 none fig 12.45x4.61 in Reference choice changes different quality endpoints
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| 54 |
+
74 none fig 12.45x4.72 in Technical repeats and follow-up are different controls
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| 55 |
+
75 none fig 12.45x5.32 in Annotation agreement and difficult categories
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| 56 |
+
76 none fig 12.45x5.39 in Depth matching changes precision and coverage
|
| 57 |
+
77 none fig 12.45x4.87 in Detection and library size are separate diagnostics
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| 58 |
+
78 right fig 9.20x5.18 in Healthy cohort: LoRA cells cover the real ones
|
| 59 |
+
79 right fig 9.20x4.79 in Healthy cohort: realism beyond precision/coverage
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| 60 |
+
80 right fig 9.20x5.14 in Healthy cohort: full vs LoRA vs condition encoder
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| 61 |
+
81 below fig 9.37x4.63 in Representative-dependent composition
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| 62 |
+
82 below fig 11.39x4.63 in Full vs LoRA vs cond.-encoder-only
|
| 63 |
+
83 right fig 9.20x5.09 in Healthy cohort: LoRA rank and K
|
| 64 |
+
84 right fig 9.20x5.09 in Healthy paired-data learning curves
|
| 65 |
+
85 right fig 9.20x4.66 in Time: days for scSemiProfiler, minutes for LoRA
|
| 66 |
+
86 below fig 10.77x4.63 in 5 donors: time to apply
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| 67 |
+
87 below fig 9.99x4.63 in Pairs needed: composition, coverage, training steps
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| 68 |
+
88 below fig 10.08x4.63 in LoRA rank: r = 4, 16, 64
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| 69 |
+
89 right fig 8.31x5.70 in K diversification: no gain
|
| 70 |
+
90 below fig 12.45x3.82 in Five paired cohorts
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| 71 |
+
91 none fig 12.45x4.70 in Sepsis: exact-five reconstruction across five draws
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| 72 |
+
92 none fig 12.45x5.18 in Sepsis: realism beyond precision and coverage
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| 73 |
+
93 none fig 12.45x4.70 in Imperial: first completed exact-five comparison
|
| 74 |
+
94 below fig 10.01x4.63 in 5 donors: LoRA vs scSemiProfiler — cells
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| 75 |
+
95 below fig 10.04x4.63 in 5 donors: realism beyond precision/coverage
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| 76 |
+
96 below fig 10.02x4.63 in 5 donors: precision/coverage at k = 3, 5, 10
|
| 77 |
+
97 below fig 10.09x4.63 in 5-fold: realism beyond precision/coverage
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| 78 |
+
98 below fig 11.74x4.63 in Same training pairs: LoRA vs scSemiProfiler
|
| 79 |
+
99 below fig 11.85x4.63 in scSemiProfiler and the representative-copy baseline
|
| 80 |
+
100 none fig 10.46x5.70 in Sepsis: patient-aware disease-gene agreement
|
| 81 |
+
101 none fig 10.46x5.70 in Imperial: patient-aware disease-gene agreement
|
| 82 |
+
102 below fig 10.60x4.63 in Sepsis: fine-tuning variants
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| 83 |
+
103 right fig 8.44x5.70 in Pairs needed: donor and disease signal
|
| 84 |
+
104 below fig 10.53x4.63 in Cell-type deconvolution, same pairs: composition
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| 85 |
+
105 none fig 12.45x4.94 in Deconvolution: expression coverage limits the comparison
|
| 86 |
+
106 none fig 12.45x5.08 in K=4,000 recipe: paired reconstruction quality
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| 87 |
+
107 none fig 12.45x5.08 in K=4,000 recipe: disease signal does not improve uniformly
|
| 88 |
+
108 none fig 12.45x5.22 in K=4,000 recipe: calibration gains are selective
|
| 89 |
+
109 none fig 12.45x4.66 in Influenza: response order versus response genes
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| 90 |
+
110 none fig 10.30x5.70 in COVID: calibration on a shared real-cell map
|
| 91 |
+
111 none fig 10.82x5.70 in COVID monocytes: direction after depth matching
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| 92 |
+
112 none fig 11.44x5.70 in COVID monocytes: direction, magnitude and null
|
| 93 |
+
113 none fig 11.44x5.70 in COVID CD14 monocytes: direction, magnitude and null
|
| 94 |
+
114 none fig 12.45x5.02 in COVID: biological endpoints give a mixed verdict
|
| 95 |
+
115 none fig 11.83x5.70 in Rare-state frequencies in observed cells
|
| 96 |
+
116 none fig 11.35x5.70 in Rare-state misses: rules 1–8
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| 97 |
+
117 none fig 11.72x5.70 in Rare-state misses: rules 9–15
|
| 98 |
+
118 none fig 12.06x5.70 in Rare-state fidelity: zero-aware reanalysis
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| 99 |
+
119 none fig 10.76x5.70 in Sepsis rare states across paired-data budgets
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| 100 |
+
120 none fig 12.45x5.62 in Sepsis rare-state direction across support budgets
|
| 101 |
+
121 none fig 11.35x5.70 in Rare-state screen in DRESS, Kawasaki and SLE
|
| 102 |
+
122 right fig 7.24x5.70 in Consequence: disease direction flips
|
| 103 |
+
123 none fig 12.45x5.18 in C1Q: single-gene detection versus co-detection
|
| 104 |
+
124 none fig 12.45x4.55 in Behçet: K=4,000 changes direction more than identity
|
| 105 |
+
125 none fig 12.45x5.59 in Behcet: one-gene and multi-gene C1Q rules
|
| 106 |
+
126 below fig 9.46x4.63 in Pairs from other cohorts do not transfer
|
| 107 |
+
127 below fig 9.44x4.63 in Longer training on other cohorts: gap stays
|
| 108 |
+
128 below fig 10.61x4.63 in No pretraining: same cohort, from scratch
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| 109 |
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129 below fig 10.53x4.63 in No pretraining: other cohorts, from scratch
|
| 110 |
+
130 below fig 10.20x4.63 in Rare states: from scratch vs pretrained
|
| 111 |
+
131 below fig 10.12x4.63 in Appendix: scSemiProfiler without output threshold
|
| 112 |
+
132 none fig 12.45x5.28 in Bulk-only exploration: calibration populations differ
|
| 113 |
+
134 right fig 9.20x5.19 in Rare-state fractions: original analysis
|
| 114 |
+
135 right fig 9.20x5.01 in Rare-state ranking: original analysis
|
| 115 |
+
136 below fig 9.23x4.98 in Rare states: original five-fold analysis
|
| 116 |
+
137 right fig 8.01x5.70 in Bulk-only cohort plan: original snapshot
|
| 117 |
+
138 none fig 12.45x4.73 in Historical bulk-only search: no confirmed new finding
|
| 118 |
+
140 below fig 12.45x4.62 in Next: other tissues from a few dozen pairs
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| 119 |
+
{"slides": 140, "groups": {"Introduction": [1, 2, 3, 4], "Figure 1": [5, 6, 7, 8, 9, 10], "Figure 2": [11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23], "Figure 3": [24, 25, 26, 27, 28, 29, 30, 31, 32, 33], "Figure 4": [34, 35, 36, 37, 38, 39], "Figure 5": [40, 41], "Figure 6": [42, 43, 44], "Supplementary": [45, 46], "Supp S01": [47, 48, 49, 50, 51, 52], "Supp S02": [53, 54, 55, 56, 57], "Supp S03": [58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72], "Supp S04": [73, 74, 75, 76, 77], "Supp S05": [78, 79, 80, 81, 82], "Supp S06": [83, 84, 85, 86, 87, 88, 89], "Supp S07": [90, 91, 92, 93, 94, 95, 96, 97, 98, 99], "Supp S08": [100, 101, 102, 103, 104, 105, 106, 107, 108], "Supp S09": [109, 110, 111, 112, 113, 114], "Supp S10": [115, 116, 117, 118, 119, 120], "Supp S11": [121, 122, 123, 124, 125], "Supp S12": [126, 127, 128, 129, 130], "Supp S13": [131], "Supp S14": [132], "Historical archive": [133, 134, 135, 136, 137, 138], "Discussion": [139, 140]}, "pptx": "/home/sj_server_1/PBISC/immun-pbmc-fm/model_8_sparse_data_diffusion/presentations/2026-09-30--paper-summary--r00/PBISC-Diffusion_expanded_master_20261013_enriched.pptx"}
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| 120 |
+
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_20261013_enriched.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_20261013_enriched.pdf using filter : impress_pdf_Export:{"UseTaggedPDF":{"type":"boolean","value":"false"},"PDFUACompliance":{"type":"boolean","value":"false"}}
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| 121 |
+
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_20261013_enriched.pdf
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| 122 |
+
{"pass": true, "counts": {"spec": 140, "pptx": 140, "pdf": 140}, "failures": [], "contacts": 12}
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| 123 |
+
7 right fig 9.20x4.86 in Experimental overview
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| 124 |
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8 below fig 12.45x2.62 in Pretraining corpus
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| 125 |
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9 below fig 12.38x5.33 in Corpus scale and generation workflow
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| 126 |
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10 none fig 12.45x4.07 in From Gaussian noise to generated cell states
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| 127 |
+
13 none fig 12.45x5.67 in Where context width and trunk width change
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| 128 |
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14 none fig 12.45x5.67 in Predicted and oracle hints: one trained denoiser
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| 129 |
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15 none fig 12.45x5.67 in Architecture: full and late validation progression
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| 130 |
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16 below fig 9.57x4.63 in Width & context ablation: benchmark
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| 131 |
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17 none fig 12.45x5.67 in Architecture arms: dimensions and endpoints
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| 132 |
+
18 below fig 9.57x4.63 in Gene context: 2k / 3k / 6k / 15k
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| 133 |
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19 none fig 12.45x5.67 in Gene panels: progression relative to each endpoint
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| 134 |
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20 none fig 12.45x5.67 in Gene-panel arms: exact sizes and training provenance
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| 135 |
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21 none fig 12.45x5.67 in All ablation arms: parameters and training time
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| 136 |
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22 none fig 12.15x5.70 in Real-cell repeat: a sampling reference
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| 137 |
+
23 none fig 12.45x5.47 in Native-pseudobulk model comparisons
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| 138 |
+
26 none fig 11.76x5.70 in Bulk and pooled cells: different expression values
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| 139 |
+
27 none fig 12.45x5.18 in Paired calibration reduces same-donor expression error
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| 140 |
+
28 below fig 10.47x4.63 in Consequence: cells off-manifold
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| 141 |
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29 none fig 12.15x5.70 in Healthy paired data: full FT and LoRA
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| 142 |
+
30 none fig 12.45x5.40 in Full FT and LoRA ranks: quality and parameters
|
| 143 |
+
31 right fig 9.20x5.63 in Healthy paired-data budget: n training + 7 validation
|
| 144 |
+
32 right fig 9.20x5.17 in Five pairs, no extra validation: LoRA vs scSemi
|
| 145 |
+
33 none fig 12.17x5.70 in Composition: error and donor-level wins
|
| 146 |
+
36 right fig 9.20x5.18 in Disease signals with five training donors
|
| 147 |
+
37 right fig 9.20x4.80 in 5-fold CV: disease signal
|
| 148 |
+
38 below fig 11.93x4.63 in Disease genes at every list length (CAT)
|
| 149 |
+
39 below fig 10.54x4.63 in Cell-type deconvolution, same pairs: disease signal
|
| 150 |
+
47 below fig 12.45x4.61 in Backbone: SDD → PBISC-Diffusion
|
| 151 |
+
48 below fig 12.45x4.61 in Bulk conditioning
|
| 152 |
+
49 below fig 11.68x5.33 in Denoiser: joint value + support diffusion
|
| 153 |
+
50 below fig 12.45x4.71 in Fine-tuning with paired bulk + sc
|
| 154 |
+
51 below fig 12.35x4.63 in Evaluation design
|
| 155 |
+
52 below fig 11.19x4.63 in How we score generated cells
|
| 156 |
+
53 none fig 12.45x5.31 in Does the model follow its bulk conditioning?
|
| 157 |
+
54 below fig 10.30x4.63 in SLE benchmark: PBISC vs scSemiProfiler
|
| 158 |
+
55 below fig 10.79x4.63 in SLE benchmark: per cell type
|
| 159 |
+
56 none fig 12.45x5.38 in Disjoint-cell controls test the bulk-broadcast baseline
|
| 160 |
+
57 none fig 12.45x5.60 in SLE: what is added beyond the bulk broadcast?
|
| 161 |
+
58 below fig 12.45x5.24 in Same shift in three paired cohorts
|
| 162 |
+
59 none fig 12.45x5.64 in Input corrections on one real-reference UMAP
|
| 163 |
+
60 none fig 12.45x4.86 in Where generated-cell density differs from real cells
|
| 164 |
+
61 none fig 12.45x4.89 in Input calibration changes cell-type composition
|
| 165 |
+
62 none fig 12.45x5.63 in Same noise, different input: matched-cell shifts
|
| 166 |
+
63 none fig 12.45x4.76 in Matched noise separates cell state from cell identity
|
| 167 |
+
64 none fig 12.45x5.63 in Input changes can switch the generated cell label
|
| 168 |
+
65 none fig 12.45x5.58 in Nearest real cells: distance and label agreement
|
| 169 |
+
66 none fig 12.34x5.70 in Composition agreement does not ensure state agreement
|
| 170 |
+
67 none fig 12.45x5.47 in Gene-length effects in the bulk input
|
| 171 |
+
68 none fig 12.45x5.47 in Gene-length effects within label-stable cells
|
| 172 |
+
69 none fig 12.45x5.41 in Raw and TPM shifts persist within cell labels
|
| 173 |
+
70 none fig 12.40x5.70 in Reference calibration leaves specific gene-state shifts
|
| 174 |
+
71 none fig 12.45x5.45 in Donor trait axes and donor identification differ
|
| 175 |
+
72 none fig 12.45x4.61 in Reference choice changes different quality endpoints
|
| 176 |
+
74 none fig 12.45x4.72 in Technical repeats and follow-up are different controls
|
| 177 |
+
75 none fig 12.45x5.32 in Annotation agreement and difficult categories
|
| 178 |
+
76 none fig 12.45x5.39 in Depth matching changes precision and coverage
|
| 179 |
+
77 none fig 12.45x4.87 in Detection and library size are separate diagnostics
|
| 180 |
+
78 right fig 9.20x5.18 in Healthy cohort: LoRA cells cover the real ones
|
| 181 |
+
79 right fig 9.20x4.79 in Healthy cohort: realism beyond precision/coverage
|
| 182 |
+
80 right fig 9.20x5.14 in Healthy cohort: full vs LoRA vs condition encoder
|
| 183 |
+
81 below fig 9.37x4.63 in Representative-dependent composition
|
| 184 |
+
82 below fig 11.39x4.63 in Full vs LoRA vs cond.-encoder-only
|
| 185 |
+
83 right fig 9.20x5.09 in Healthy cohort: LoRA rank and K
|
| 186 |
+
84 right fig 9.20x5.09 in Healthy paired-data learning curves
|
| 187 |
+
85 right fig 9.20x4.66 in Time: days for scSemiProfiler, minutes for LoRA
|
| 188 |
+
86 below fig 10.77x4.63 in 5 donors: time to apply
|
| 189 |
+
87 below fig 9.99x4.63 in Pairs needed: composition, coverage, training steps
|
| 190 |
+
88 below fig 10.08x4.63 in LoRA rank: r = 4, 16, 64
|
| 191 |
+
89 right fig 8.31x5.70 in K diversification: no gain
|
| 192 |
+
90 below fig 12.45x3.82 in Five paired cohorts
|
| 193 |
+
91 none fig 12.45x4.70 in Sepsis: exact-five reconstruction across five draws
|
| 194 |
+
92 none fig 12.45x5.18 in Sepsis: realism beyond precision and coverage
|
| 195 |
+
93 none fig 12.45x4.70 in Imperial: first completed exact-five comparison
|
| 196 |
+
94 below fig 10.01x4.63 in 5 donors: LoRA vs scSemiProfiler — cells
|
| 197 |
+
95 below fig 10.04x4.63 in 5 donors: realism beyond precision/coverage
|
| 198 |
+
96 below fig 10.02x4.63 in 5 donors: precision/coverage at k = 3, 5, 10
|
| 199 |
+
97 below fig 10.09x4.63 in 5-fold: realism beyond precision/coverage
|
| 200 |
+
98 below fig 11.74x4.63 in Same training pairs: LoRA vs scSemiProfiler
|
| 201 |
+
99 below fig 11.85x4.63 in scSemiProfiler and the representative-copy baseline
|
| 202 |
+
100 none fig 10.46x5.70 in Sepsis: patient-aware disease-gene agreement
|
| 203 |
+
101 none fig 10.46x5.70 in Imperial: patient-aware disease-gene agreement
|
| 204 |
+
102 below fig 10.60x4.63 in Sepsis: fine-tuning variants
|
| 205 |
+
103 right fig 8.44x5.70 in Pairs needed: donor and disease signal
|
| 206 |
+
104 below fig 10.53x4.63 in Cell-type deconvolution, same pairs: composition
|
| 207 |
+
105 none fig 12.45x4.94 in Deconvolution: expression coverage limits the comparison
|
| 208 |
+
106 none fig 12.45x5.08 in K=4,000 recipe: paired reconstruction quality
|
| 209 |
+
107 none fig 12.45x5.08 in K=4,000 recipe: disease signal does not improve uniformly
|
| 210 |
+
108 none fig 12.45x5.22 in K=4,000 recipe: calibration gains are selective
|
| 211 |
+
109 none fig 12.45x4.66 in Influenza: response order versus response genes
|
| 212 |
+
110 none fig 10.30x5.70 in COVID: calibration on a shared real-cell map
|
| 213 |
+
111 none fig 10.82x5.70 in COVID monocytes: direction after depth matching
|
| 214 |
+
112 none fig 11.44x5.70 in COVID monocytes: direction, magnitude and null
|
| 215 |
+
113 none fig 11.44x5.70 in COVID CD14 monocytes: direction, magnitude and null
|
| 216 |
+
114 none fig 12.45x5.02 in COVID: biological endpoints give a mixed verdict
|
| 217 |
+
115 none fig 11.83x5.70 in Rare-state frequencies in observed cells
|
| 218 |
+
116 none fig 11.35x5.70 in Rare-state misses: rules 1–8
|
| 219 |
+
117 none fig 11.72x5.70 in Rare-state misses: rules 9–15
|
| 220 |
+
118 none fig 12.06x5.70 in Rare-state fidelity: zero-aware reanalysis
|
| 221 |
+
119 none fig 10.76x5.70 in Sepsis rare states across paired-data budgets
|
| 222 |
+
120 none fig 12.45x5.62 in Sepsis rare-state direction across support budgets
|
| 223 |
+
121 none fig 11.35x5.70 in Rare-state screen in DRESS, Kawasaki and SLE
|
| 224 |
+
122 right fig 7.24x5.70 in Consequence: disease direction flips
|
| 225 |
+
123 none fig 12.45x5.18 in C1Q: single-gene detection versus co-detection
|
| 226 |
+
124 none fig 12.45x4.55 in Behçet: K=4,000 changes direction more than identity
|
| 227 |
+
125 none fig 12.45x5.59 in Behcet: one-gene and multi-gene C1Q rules
|
| 228 |
+
126 below fig 9.46x4.63 in Pairs from other cohorts do not transfer
|
| 229 |
+
127 below fig 9.44x4.63 in Longer training on other cohorts: gap stays
|
| 230 |
+
128 below fig 10.61x4.63 in No pretraining: same cohort, from scratch
|
| 231 |
+
129 below fig 10.53x4.63 in No pretraining: other cohorts, from scratch
|
| 232 |
+
130 below fig 10.20x4.63 in Rare states: from scratch vs pretrained
|
| 233 |
+
131 below fig 10.12x4.63 in Appendix: scSemiProfiler without output threshold
|
| 234 |
+
132 none fig 12.45x5.28 in Bulk-only exploration: calibration populations differ
|
| 235 |
+
134 right fig 9.20x5.19 in Rare-state fractions: original analysis
|
| 236 |
+
135 right fig 9.20x5.01 in Rare-state ranking: original analysis
|
| 237 |
+
136 below fig 9.23x4.98 in Rare states: original five-fold analysis
|
| 238 |
+
137 right fig 8.01x5.70 in Bulk-only cohort plan: original snapshot
|
| 239 |
+
138 none fig 12.45x4.73 in Historical bulk-only search: no confirmed new finding
|
| 240 |
+
140 below fig 12.45x4.62 in Next: other tissues from a few dozen pairs
|
| 241 |
+
{"slides": 140, "groups": {"Introduction": [1, 2, 3, 4], "Figure 1": [5, 6, 7, 8, 9, 10], "Figure 2": [11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23], "Figure 3": [24, 25, 26, 27, 28, 29, 30, 31, 32, 33], "Figure 4": [34, 35, 36, 37, 38, 39], "Figure 5": [40, 41], "Figure 6": [42, 43, 44], "Supplementary": [45, 46], "Supp S01": [47, 48, 49, 50, 51, 52], "Supp S02": [53, 54, 55, 56, 57], "Supp S03": [58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72], "Supp S04": [73, 74, 75, 76, 77], "Supp S05": [78, 79, 80, 81, 82], "Supp S06": [83, 84, 85, 86, 87, 88, 89], "Supp S07": [90, 91, 92, 93, 94, 95, 96, 97, 98, 99], "Supp S08": [100, 101, 102, 103, 104, 105, 106, 107, 108], "Supp S09": [109, 110, 111, 112, 113, 114], "Supp S10": [115, 116, 117, 118, 119, 120], "Supp S11": [121, 122, 123, 124, 125], "Supp S12": [126, 127, 128, 129, 130], "Supp S13": [131], "Supp S14": [132], "Historical archive": [133, 134, 135, 136, 137, 138], "Discussion": [139, 140]}, "pptx": "/home/sj_server_1/PBISC/immun-pbmc-fm/model_8_sparse_data_diffusion/presentations/2026-09-30--paper-summary--r00/PBISC-Diffusion_expanded_master_20261013_enriched.pptx"}
|
| 242 |
+
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_20261013_enriched.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_20261013_enriched.pdf using filter : impress_pdf_Export:{"UseTaggedPDF":{"type":"boolean","value":"false"},"PDFUACompliance":{"type":"boolean","value":"false"}}
|
| 243 |
+
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_20261013_enriched.pdf
|
| 244 |
+
{"pass": true, "counts": {"spec": 140, "pptx": 140, "pdf": 140}, "failures": [], "contacts": 12}
|
paper-releases/pbisc-diffusion/updates/20261013T072655Z-enriched-140-slide-master/diffusion/dataset/server_1/model8/presentations/2026-09-30--paper-summary--r00/data/figure_enrichment_20261013/render.py
ADDED
|
@@ -0,0 +1,27 @@
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| 1 |
+
"""Rebuild from saved enrichment assets, export PDF and validate (CPU only).
|
| 2 |
+
|
| 3 |
+
Invoke within a bounded user-systemd unit with CUDA_VISIBLE_DEVICES empty.
|
| 4 |
+
This does not execute training, sampling or any scientific figure builder.
|
| 5 |
+
"""
|
| 6 |
+
from pathlib import Path
|
| 7 |
+
import os
|
| 8 |
+
import subprocess
|
| 9 |
+
import sys
|
| 10 |
+
|
| 11 |
+
if os.environ.get('CUDA_VISIBLE_DEVICES')!='':
|
| 12 |
+
raise SystemExit('CPU-only export requires empty CUDA_VISIBLE_DEVICES')
|
| 13 |
+
A=Path(__file__).resolve().parent
|
| 14 |
+
D=A.parents[1]
|
| 15 |
+
commands=[
|
| 16 |
+
[sys.executable,str(D/'tools/build_enriched_master_20261013.py')],
|
| 17 |
+
['libreoffice','-env:UserInstallation=file:///tmp/pbisc-enriched-lo-20261013',
|
| 18 |
+
'--headless','--convert-to',
|
| 19 |
+
'pdf:impress_pdf_Export:{"UseTaggedPDF":{"type":"boolean","value":"false"},"PDFUACompliance":{"type":"boolean","value":"false"}}',
|
| 20 |
+
'--outdir',str(D),str(D/'PBISC-Diffusion_expanded_master_20261013_enriched.pptx')],
|
| 21 |
+
[sys.executable,str(D/'tools/verify_enriched_master_20261013.py')],
|
| 22 |
+
]
|
| 23 |
+
with (A/'render.log').open('a') as log:
|
| 24 |
+
for command in commands:
|
| 25 |
+
print('Run:',Path(command[0]).name,Path(command[-1]).name,flush=True)
|
| 26 |
+
subprocess.run(command,cwd=D,stdout=log,stderr=subprocess.STDOUT,check=True,timeout=600)
|
| 27 |
+
print('PPTX, PDF and automated validation completed.',flush=True)
|