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1
+ page,parent_156_page,group,title,addition
2
+ 1,1.0,Introduction,PBISC-Diffusion: manuscript evidence,
3
+ 2,2.0,Introduction,Figures 1-6: the expanded evidence map,
4
+ 3,3.0,Introduction,How this expanded deck is organized,guide:scope
5
+ 4,4.0,Introduction,Manuscript map: the six figures,
6
+ 5,5.0,Figure 1,Figure 1. Overview and corpus,
7
+ 6,6.0,Figure 1,"Figure 1: overview, corpus and denoising",
8
+ 7,7.0,Figure 1,Experimental overview,
9
+ 8,8.0,Figure 1,Pretraining data: 33.14 million training cells,figure1b:focused_training_corpus
10
+ 9,9.0,Figure 1,Training corpus: complete counts and minor categories,figure1b:training_corpus
11
+ 10,10.0,Figure 1,"Full source corpus: training, validation and test",strengthening:corpus:0
12
+ 11,11.0,Figure 1,From 41.40M source cells to 33.14M training cells,strengthening:corpus:1
13
+ 12,12.0,Figure 1,Recipe K and training exposure are different counts,strengthening:corpus:2
14
+ 13,13.0,Figure 1,Corpus scale and generation workflow,
15
+ 14,14.0,Figure 1,From Gaussian noise to generated cell states,enrichment:trajectory_four_pca_frames
16
+ 15,15.0,Figure 2,Figure 2. SLE model ablations,
17
+ 16,16.0,Figure 2,Figure 2: architecture and gene context,
18
+ 17,17.0,Figure 2,Where context width and trunk width change,enrichment:arch_context_vs_trunk
19
+ 18,18.0,Figure 2,Predicted and oracle hints: one trained denoiser,enrichment:arch_hint_injection
20
+ 19,19.0,Figure 2,Architecture: full and late validation progression,
21
+ 20,20.0,Figure 2,Width & context ablation: benchmark,
22
+ 21,21.0,Figure 2,Architecture arms: dimensions and endpoints,enrichment:arch_width_arm_register
23
+ 22,22.0,Figure 2,Gene context: 2k / 3k / 6k / 15k,
24
+ 23,23.0,Figure 2,Gene panels: progression relative to each endpoint,enrichment:arch_panel_loss_progression
25
+ 24,24.0,Figure 2,Gene-panel arms: exact sizes and training provenance,enrichment:arch_panel_arm_register
26
+ 25,25.0,Figure 2,All ablation arms: parameters and training time,enrichment:arch_all_arm_compute
27
+ 26,26.0,Figure 2,Real-cell repeat: a sampling reference,enrichment:real_cell_repeat
28
+ 27,27.0,Figure 2,Native-pseudobulk model comparisons,review:6
29
+ 28,28.0,Figure 3,Figure 3. Real-bulk adaptation,
30
+ 29,29.0,Figure 3,Figure 3: the paired-adaptation story,
31
+ 30,30.0,Figure 3,Bulk and pooled cells: different expression values,
32
+ 31,31.0,Figure 3,Paired calibration reduces same-donor expression error,enrichment:mismatch_same_donor_errors
33
+ 32,32.0,Figure 3,Consequence: cells off-manifold,
34
+ 33,33.0,Figure 3,Adaptation recovers the observed cell mixture,strengthening:healthy:0
35
+ 34,34.0,Figure 3,Adaptation: mixture error and expression agreement,strengthening:healthy:1
36
+ 35,35.0,Figure 3,Healthy paired data: full FT and LoRA,guide:availability
37
+ 36,36.0,Figure 3,Full FT and LoRA ranks: quality and parameters,review:8
38
+ 37,37.0,Figure 3,What does “all pairs” actually mean?,strengthening:healthy:2
39
+ 38,38.0,Figure 3,Healthy pair budget: correlation in all cell types,all_celltypes:correlation
40
+ 39,39.0,Figure 3,Healthy pair budget: error in all cell types,all_celltypes:mae
41
+ 40,40.0,Figure 3,"Five pairs, no extra validation: LoRA vs scSemi",
42
+ 41,41.0,Figure 3,Composition: error and donor-level wins,review:13
43
+ 42,,Figure 3,Strict paired budget: held-out reconstruction,x1_priority:healthy_budget
44
+ 43,,Figure 3,Strict support: composition bias across all six types,x1_priority:healthy_types
45
+ 44,42.0,Figure 4,Figure 4. Disease signal preservation,
46
+ 45,43.0,Figure 4,Figure 4: disease signal preservation,
47
+ 46,44.0,Figure 4,Disease signals with five training donors,
48
+ 47,45.0,Figure 4,5-fold CV: disease signal,
49
+ 48,46.0,Figure 4,Disease genes at every list length (CAT),
50
+ 49,47.0,Figure 4,"Cell-type deconvolution, same pairs: disease signal",
51
+ 50,48.0,Figure 4,Disease gene rankings: complete CV comparison,strengthening:disease_metrics:0
52
+ 51,49.0,Figure 4,Disease integrity depends on cohort and endpoint,strengthening:disease_metrics:1
53
+ 52,50.0,Figure 4,Five-pair Sepsis: metrics across all support draws,strengthening:disease_metrics:2
54
+ 53,,Figure 4,Sepsis: strict five-pair disease integrity,x1_priority:disease_ye2026_sepsis
55
+ 54,,Figure 4,Imperial ESKD: strict five-pair disease integrity,x1_priority:disease_imperial_eskd
56
+ 55,,Figure 4,Giroux: strict five-pair disease integrity,x1_priority:disease_giroux2022
57
+ 56,,Figure 4,CHILI: completed core disease metrics,x1_priority:disease_ji2025_chili
58
+ 57,51.0,Figure 5,Figure 5. Rare-population identity,
59
+ 58,52.0,Figure 5,Figure 5: paired rare-population identity,
60
+ 59,53.0,Figure 5,Figure 5 targets begin with the source paper,strengthening:rare_literature:0
61
+ 60,54.0,Figure 5,Ye sepsis: published markers in paired scRNA,strengthening:rare_literature:1
62
+ 61,55.0,Figure 5,Transcriptional programs and rare-population identity,strengthening:rare_literature:2
63
+ 62,56.0,Figure 6,Figure 6. Published-finding reproduction,
64
+ 63,57.0,Figure 6,Figure 6: published-finding reproduction,
65
+ 64,58.0,Figure 6,Figure 6: what the reproduction must establish,guide:figure6
66
+ 65,59.0,Supplementary,Supplementary evidence,
67
+ 66,60.0,Supplementary,Supplementary evidence map,
68
+ 67,61.0,Supp S01,Corpus reference: assay and source composition,
69
+ 68,62.0,Supp S01,Backbone: SDD → PBISC-Diffusion,
70
+ 69,63.0,Supp S01,Bulk conditioning,
71
+ 70,64.0,Supp S01,Denoiser: joint value + support diffusion,
72
+ 71,65.0,Supp S01,Fine-tuning with paired bulk + sc,
73
+ 72,66.0,Supp S01,Evaluation design,
74
+ 73,67.0,Supp S01,How we score generated cells,
75
+ 74,68.0,Supp S02,Does the model follow its bulk conditioning?,healthy_sle_conditioning_interventions
76
+ 75,69.0,Supp S02,SLE benchmark: PBISC vs scSemiProfiler,
77
+ 76,70.0,Supp S02,SLE benchmark: per cell type,
78
+ 77,71.0,Supp S02,Disjoint-cell controls test the bulk-broadcast baseline,healthy_sle_disjoint_truth_control
79
+ 78,72.0,Supp S02,SLE: what is added beyond the bulk broadcast?,disease_sle_broadcast
80
+ 79,73.0,Supp S03,Same shift in three paired cohorts,
81
+ 80,74.0,Supp S03,Input corrections on one real-reference UMAP,healthy_stored_real_reference_umap
82
+ 81,75.0,Supp S03,Where generated-cell density differs from real cells,healthy_saved_density_difference
83
+ 82,76.0,Supp S03,Input calibration changes cell-type composition,healthy_input_control_composition
84
+ 83,77.0,Supp S03,"Same noise, different input: matched-cell shifts",healthy_stored_matched_trajectories
85
+ 84,78.0,Supp S03,Matched noise separates cell state from cell identity,healthy_matched_similarity
86
+ 85,79.0,Supp S03,Input changes can switch the generated cell label,healthy_label_transitions
87
+ 86,80.0,Supp S03,Nearest real cells: distance and label agreement,healthy_nearest_real_by_type
88
+ 87,81.0,Supp S03,Composition agreement does not ensure state agreement,healthy_within_type_centroids
89
+ 88,82.0,Supp S03,Gene-length effects in the bulk input,healthy_gene_length_input
90
+ 89,83.0,Supp S03,Gene-length effects within label-stable cells,healthy_gene_length_stable
91
+ 90,84.0,Supp S03,Raw and TPM shifts persist within cell labels,healthy_raw_tpm_top_genes
92
+ 91,85.0,Supp S03,Reference calibration leaves specific gene-state shifts,healthy_refcal_top_genes
93
+ 92,86.0,Supp S03,Donor trait axes and donor identification differ,healthy_donor_axes
94
+ 93,87.0,Supp S03,Reference choice changes different quality endpoints,healthy_reference_choice
95
+ 94,88.0,Supp S04,Why the historical and strict protocols differ,guide:protocol
96
+ 95,89.0,Supp S04,Technical repeats and follow-up are different controls,healthy_immicro_replicate_controls
97
+ 96,90.0,Supp S04,Annotation agreement and difficult categories,healthy_annotation_agreement
98
+ 97,91.0,Supp S04,Depth matching changes precision and coverage,healthy_depth_matched_quality
99
+ 98,92.0,Supp S04,Detection and library size are separate diagnostics,healthy_detection_and_library
100
+ 99,93.0,Supp S05,Healthy cohort: LoRA cells cover the real ones,
101
+ 100,94.0,Supp S05,Healthy cohort: realism beyond precision/coverage,
102
+ 101,95.0,Supp S05,Healthy cohort: full vs LoRA vs condition encoder,
103
+ 102,96.0,Supp S05,Representative-dependent composition,
104
+ 103,97.0,Supp S05,Full vs LoRA vs cond.-encoder-only,
105
+ 104,98.0,Supp S06,"Pair-budget summary: composition, coverage and steps",
106
+ 105,99.0,Supp S06,Healthy cohort: LoRA rank and K,
107
+ 106,100.0,Supp S06,Healthy paired-data learning curves,
108
+ 107,101.0,Supp S06,"Time: days for scSemiProfiler, minutes for LoRA",
109
+ 108,102.0,Supp S06,5 donors: time to apply,
110
+ 109,103.0,Supp S06,"Pairs needed: composition, coverage, training steps",
111
+ 110,104.0,Supp S06,"LoRA rank: r = 4, 16, 64",
112
+ 111,105.0,Supp S06,K diversification: no gain,
113
+ 112,106.0,Supp S07,Five paired cohorts,
114
+ 113,107.0,Supp S07,Sepsis: exact-five reconstruction across five draws,disease_strict_sepsis_quality
115
+ 114,108.0,Supp S07,Sepsis: realism beyond precision and coverage,disease_strict_sepsis_realism
116
+ 115,109.0,Supp S07,Imperial: first completed exact-five comparison,disease_strict_imperial_quality
117
+ 116,110.0,Supp S07,5 donors: LoRA vs scSemiProfiler — cells,
118
+ 117,111.0,Supp S07,5 donors: realism beyond precision/coverage,
119
+ 118,112.0,Supp S07,"5 donors: precision/coverage at k = 3, 5, 10",
120
+ 119,113.0,Supp S07,5-fold: realism beyond precision/coverage,
121
+ 120,114.0,Supp S07,Same training pairs: LoRA vs scSemiProfiler,
122
+ 121,115.0,Supp S07,scSemiProfiler and the representative-copy baseline,
123
+ 122,,Supp S07,PBISC x1: completed evidence and remaining units,x1_priority:availability
124
+ 123,,Supp S07,Sepsis: full realism and depth controls,x1_priority:extras_ye2026_sepsis
125
+ 124,,Supp S07,Imperial ESKD: full realism and depth controls,x1_priority:extras_imperial_eskd
126
+ 125,,Supp S07,Giroux: full realism and depth controls,x1_priority:extras_giroux2022
127
+ 126,116.0,Supp S08,Sepsis: patient-aware disease-gene agreement,disease_strict_ye2026_sepsis_deg
128
+ 127,117.0,Supp S08,Imperial: patient-aware disease-gene agreement,disease_strict_imperial_eskd_deg
129
+ 128,118.0,Supp S08,Sepsis: fine-tuning variants,
130
+ 129,119.0,Supp S08,Pairs needed: donor and disease signal,
131
+ 130,120.0,Supp S08,"Cell-type deconvolution, same pairs: composition",
132
+ 131,121.0,Supp S08,Deconvolution: expression coverage limits the comparison,disease_deconv_expression_coverage
133
+ 132,122.0,Supp S08,"K=4,000 recipe: paired reconstruction quality",disease_k4000_quality
134
+ 133,123.0,Supp S08,"K=4,000 recipe: disease signal does not improve uniformly",disease_k4000_disease
135
+ 134,124.0,Supp S08,"K=4,000 recipe: calibration gains are selective",disease_k4000_calibration
136
+ 135,,Supp S08,Patient-aware DEG: same support and test samples,x1_priority:donor_deg
137
+ 136,,Supp S08,"Paired donor uncertainty: saved 2,000-bootstrap intervals",x1_priority:donor_intervals
138
+ 137,,Supp S08,Giroux: PBISC x1 donor uncertainty,x1_priority:individual_ci_giroux2022
139
+ 138,125.0,Supp S09,Influenza: response order versus response genes,disease_influenza_response
140
+ 139,126.0,Supp S09,COVID: calibration on a shared real-cell map,disease_covid_map
141
+ 140,127.0,Supp S09,COVID monocytes: direction after depth matching,disease_covid_direction
142
+ 141,128.0,Supp S09,"COVID monocytes: direction, magnitude and null",disease_covid_monocyte_direction_detail
143
+ 142,129.0,Supp S09,"COVID CD14 monocytes: direction, magnitude and null",disease_covid_cd14_direction_detail
144
+ 143,130.0,Supp S09,COVID: biological endpoints give a mixed verdict,disease_covid_endpoints
145
+ 144,131.0,Supp S10,Rare-state frequencies in observed cells,review:22
146
+ 145,132.0,Supp S10,Rare-state misses: rules 1–8,disease_rare_misses_1
147
+ 146,133.0,Supp S10,Rare-state misses: rules 9–15,disease_rare_misses_2
148
+ 147,134.0,Supp S10,Rare-state fidelity: zero-aware reanalysis,review:23
149
+ 148,135.0,Supp S10,Sepsis rare states across paired-data budgets,disease_sepsis_rare_support
150
+ 149,136.0,Supp S10,Sepsis rare-state direction across support budgets,disease_sepsis_rare_direction
151
+ 150,137.0,Supp S11,"Rare-state screen in DRESS, Kawasaki and SLE",disease_external_rare_screen
152
+ 151,138.0,Supp S11,Consequence: disease direction flips,
153
+ 152,139.0,Supp S11,C1Q: single-gene detection versus co-detection,disease_c1q_cross_disease
154
+ 153,140.0,Supp S11,"Behçet: K=4,000 changes direction more than identity",disease_behcet_k4000
155
+ 154,141.0,Supp S11,Behcet: one-gene and multi-gene C1Q rules,review:24
156
+ 155,142.0,Supp S12,Pairs from other cohorts do not transfer,
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+ 156,143.0,Supp S12,Longer training on other cohorts: gap stays,
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+ 157,144.0,Supp S12,"No pretraining: same cohort, from scratch",
159
+ 158,145.0,Supp S12,"No pretraining: other cohorts, from scratch",
160
+ 159,146.0,Supp S12,Rare states: from scratch vs pretrained,
161
+ 160,147.0,Supp S13,Appendix: scSemiProfiler without output threshold,
162
+ 161,148.0,Supp S14,Bulk-only exploration: calibration populations differ,disease_bulkonly_imperial_wave_shift
163
+ 162,149.0,Historical archive,Historical scoring and plans,
164
+ 163,150.0,Historical archive,Rare-state fractions: original analysis,
165
+ 164,151.0,Historical archive,Rare-state ranking: original analysis,
166
+ 165,152.0,Historical archive,Rare states: original five-fold analysis,
167
+ 166,153.0,Historical archive,Bulk-only cohort plan: original snapshot,
168
+ 167,154.0,Historical archive,Historical bulk-only search: no confirmed new finding,disease_bulkonly_verification_history
169
+ 168,155.0,Discussion,Discussion and outlook,
170
+ 169,156.0,Discussion,Next: other tissues from a few dozen pairs,