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pmid:33282911

A Prognostic Model of 15 Immune-Related Gene Pairs Associated With Tumor Mutation Burden for Hepatocellular Carcinoma.

Junyu Huo · Liqun Wu · Yunjin Zang

Frontiers in molecular biosciences · 2020 doi:10.3389/fmolb.2020.581354

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title
A Prognostic Model of 15 Immune-Related Gene Pairs Associated With Tumor Mutation Burden for Hepatocellular Carcinoma.
doi
10.3389/fmolb.2020.581354
pmid
33282911
authors array · 3 items
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Junyu Huo
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Liqun Wu
[2]
Yunjin Zang
journal
Frontiers in molecular biosciences
year
2020
abstract
INTRODUCTION: Tumor mutation burden (TMB) is an emerging biomarker for immunotherapy of hepatocellular carcinoma (HCC), but its value for clinical application has not been fully revealed. MATERIALS AND METHODS: We used the Wilcox test to identify the differentially expressed immune-related genes (DEIRGs) in groups with high and low TMB as well as screened the immune gene pairs related to prognosis using univariate Cox regression analysis. A LASSO Cox regression prognostic model was developed by combining The Cancer Genome Atlas Liver Hepatocellular Carcinoma (TCGA-LIHC) with the International Cancer Genome Consortium (ICGC) LIRI-JP cohort, and internal (TCGA, ICGC) and external (GSE14520) validation analyses were conducted on the predictive value of the model. We also explored the relationship between the prognostic model and tumor microenvironment via the ESTIMATE algorithm and performed clinical correlation analysis by the chi-square test, revealing its underlying molecular mechanism with the help of Gene Set Enrichment Analysis (GSEA). RESULTS: The prognostic model consisting of 15 immune gene pairs showed high predictive value for short- and long-term survival of HCC in three independent cohorts. Based on univariate multivariate Cox regression analysis, the prognostic model could be used to independently predict the prognosis in each independent cohort. The immune score, stromal score, and estimated score values were lower in the high-risk group than in the low-risk group. As shown by the chi-square test, the prognostic model exhibited an obvious correlation with the tumor stage [American Joint Committee on Cancer tumor-node-metastasis (AJCC-TNM) (p < 0.001), Barcelona Clinic Liver Cancer (BCLC) (p = 0.003)], histopathological grade (p = 0.033), vascular invasion (p = 0.009), maximum tumor diameter (p = 0.013), and background of liver cirrhosis (p < 0.001). GSEA revealed that the high-risk group had an enrichment of many oncology features, including the cell cycle, mismatch repair, DNA replication, RNA degradation, etc. CONCLUSION: Our research developed and validated a reliable prognostic model associated with TMB for HCC, which may help to further enrich the therapeutic targets of HCC.
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A LASSO Cox regression prognostic model was developed by combining The Cancer Genome Atlas Liver Hepatocellular Carcinoma (TCGA-LIHC) with the International Cancer Genome Consortium (ICGC) LIRI-JP cohort, and internal (TCGA, ICGC) and external (GSE14520) validation analyses were conducted on the predictive value of the model.
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A LASSO Cox regression prognostic model was developed by combining The Cancer Genome Atlas Liver Hepatocellular Carcinoma (TCGA-LIHC) with the International Cancer Genome Consortium (ICGC) LIRI-JP cohort, and internal (TCGA, ICGC) and external (GSE14520) validation analyses were conducted on the predictive value of the model.
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The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
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Homo sapiens
title
Gene expression data of human hepatocellular carcinoma (HCC)
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
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The list and coef of IGPs.
structure object · 5 fields
pmcid
PMC7691640
section_index
14
section_title
LASSO Cox Regression IGP Prognostic Model Construction
row_count
16
column_count
2
table object · 8 fields
label
TABLE 1
caption
The list and coef of IGPs.
rows array · 16 items
[0] array · 2 items
[0]
IGPs
[1]
Coef
[1] array · 2 items
[0]
BLNK| ESM1
[1]
−0.556894158
[2] array · 2 items
[0]
BLNK| LYN
[1]
−0.541824561
[3] array · 2 items
[0]
CIITA| IL2RA
[1]
−0.401209687
[4] array · 2 items
[0]
CSPG5| TNFSF8
[1]
0.474599318
[5] array · 2 items
[0]
CTSS| ICAM1
[1]
−0.305089132
[6] array · 2 items
[0]
ENG| TNFAIP3
[1]
−0.660506625
[7] array · 2 items
[0]
EREG| PLXNB3
[1]
0.525553186
[8] array · 2 items
[0]
FGR| NGFR
[1]
0.377839595
[9] array · 2 items
[0]
FLT4| IL7
[1]
−0.317118995
[10] array · 2 items
[0]
FLT4| S100A2
[1]
0.836862911
[11] array · 2 items
[0]
HCK| IKBKE
[1]
−0.50853469
[12] array · 2 items
[0]
INHA| RXRG
[1]
0.50223053
[13] array · 2 items
[0]
INS| S100A2
[1]
−1.116354541
[14] array · 2 items
[0]
KCNH2| TNFSF8
[1]
0.347981123
[15] array · 2 items
[0]
PTX3| TNFSF8
[1]
0.710891356
locator
section[14]/table-wrap[1]#T1
[3] object · 16 fields
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The chi-square test of the relation between risk score and clinical features in TCGA cohort.
structure object · 5 fields
pmcid
PMC7691640
section_index
18
section_title
Clinical Correlation Analysis of the Prognostic Model
row_count
32
column_count
5
table object · 8 fields
label
TABLE 2
caption
The chi-square test of the relation between risk score and clinical features in TCGA cohort.
rows array · 32 items
[0] array · 4 items
[0]
Clinical feature
[1]
Risk score
[2]
c2
[3]
p
[1] array · 5 items
[0]
[1]
High risk n(%)
[2]
Low risk n(%)
[3]
[4]
[2] array · 5 items
[0]
Age
[1]
[2]
[3]
0.037
[4]
0.848
[3] array · 5 items
[0]
>65
[1]
72(59.02%)
[2]
50(40.98%)
[3]
[4]
[4] array · 5 items
[0]
≤65
[1]
124(57.94%)
[2]
90(42.06%)
[3]
[4]
[5] array · 5 items
[0]
Gender
[1]
[2]
[3]
3.244
[4]
0.072
[6] array · 5 items
[0]
MALE
[1]
126(55.02%)
[2]
103(44.98%)
[3]
[4]
[7] array · 5 items
[0]
FEMALE
[1]
70(65.42%)
[2]
37(34.58%)
[3]
[4]
[8] array · 5 items
[0]
Histologic_grade
[1]
[2]
[3]
4.543
[4]
0.033
[9] array · 5 items
[0]
G1-2
[1]
112(53.59%)
[2]
97(46.41%)
[3]
[4]
[10] array · 5 items
[0]
G3-4
[1]
80(65.57%)
[2]
42(34.43%)
[3]
[4]
[11] array · 3 items
[0]
New_tumor_event_after_initial_treatment
[1]
0.643
[2]
0.423
[12] array · 5 items
[0]
YES
[1]
98(59.76%)
[2]
66(40.24%)
[3]
[4]
[13] array · 5 items
[0]
NO
[1]
88(55.35%)
[2]
71(44.65%)
[3]
[4]
[14] array · 5 items
[0]
Pathologic_stage
[1]
[2]
[3]
3.703
[4]
0.054
[15] array · 5 items
[0]
Stage I–II
[1]
129(54.89%)
[2]
106(45.11%)
[3]
[4]
[16] array · 5 items
[0]
Stage III–IV
[1]
55(67.07%)
[2]
27(32.93%)
[3]
[4]
[17] array · 3 items
[0]
Person_neoplasm_cancer_status
[1]
2.846
[2]
0.092
[18] array · 5 items
[0]
WITH TUMOR
[1]
91(62.76%)
[2]
54(37.24%)
[3]
[4]
[19] array · 5 items
[0]
TUMOR FREE
[1]
94(53.41%)
[2]
82(46.59%)
[3]
[4]
[20] array · 5 items
[0]
BMI
[1]
[2]
[3]
0.566
[4]
0.452
[21] array · 5 items
[0]
>25
[1]
82(55.03%)
[2]
67(44.97%)
[3]
[4]
[22] array · 5 items
[0]
≤25
[1]
96(59.26%)
[2]
66(40.74%)
[3]
[4]
[23] array · 5 items
[0]
Race
[1]
[2]
[3]
1.861
[4]
0.172
[24] array · 5 items
[0]
White
[1]
89(54.27%)
[2]
75(45.73%)
[3]
[4]
[25] array · 5 items
[0]
Asian and others
[1]
100(61.73%)
[2]
62(38.27%)
[3]
[4]
[26] array · 5 items
[0]
Vascular tumor cell type
[1]
[2]
[3]
6.887
[4]
0.009
[27] array · 5 items
[0]
None
[1]
94(51.09%)
[2]
90(48.91%)
[3]
[4]
[28] array · 5 items
[0]
Micro-Macro
[1]
66(67.35%)
[2]
32(32.65%)
[3]
[4]
[29] array · 5 items
[0]
Prior_malignancy
[1]
[2]
[3]
0.57
[4]
0.45
[30] array · 5 items
[0]
No
[1]
181(58.96%)
[2]
126(41.04%)
[3]
[4]
[31] array · 5 items
[0]
Yes
[1]
15(51.72%)
[2]
14(48.28%)
[3]
[4]
locator
section[18]/table-wrap[1]#T2
[4] object · 16 fields
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asset:table:pmid:33282911:3
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The chi-square test of the relation between risk score and clinical features in ICGC cohort.
structure object · 5 fields
pmcid
PMC7691640
section_index
18
section_title
Clinical Correlation Analysis of the Prognostic Model
row_count
14
column_count
5
table object · 8 fields
label
TABLE 3
caption
The chi-square test of the relation between risk score and clinical features in ICGC cohort.
rows array · 14 items
[0] array · 4 items
[0]
Clinical feature
[1]
Risk score
[2]
c2
[3]
p
[1] array · 5 items
[0]
[1]
High risk n(%)
[2]
Low risk n(%)
[3]
[4]
[2] array · 5 items
[0]
Age
[1]
[2]
[3]
0.856
[4]
0.355
[3] array · 5 items
[0]
>65
[1]
49(35.25%)
[2]
90(64.75%)
[3]
[4]
[4] array · 5 items
[0]
≤65
[1]
36(41.38%)
[2]
51(58.62%)
[3]
[4]
[5] array · 5 items
[0]
Gender
[1]
[2]
[3]
0.023
[4]
0.881
[6] array · 5 items
[0]
MALE
[1]
53(34.42%)
[2]
101(65.58%)
[3]
[4]
[7] array · 5 items
[0]
FEMALE
[1]
20(33.33%)
[2]
40(66.67%)
[3]
[4]
[8] array · 5 items
[0]
Prior malignancy
[1]
[2]
[3]
0.201
[4]
0.654
[9] array · 5 items
[0]
Yes
[1]
12(41.38%)
[2]
17(58.62%)
[3]
[4]
[10] array · 5 items
[0]
No
[1]
73(37.06%)
[2]
124(62.95%)
[3]
[4]
[11] array · 5 items
[0]
Stage
[1]
[2]
[3]
10.132
[4]
0.001
[12] array · 5 items
[0]
I–II
[1]
41(29.50%)
[2]
98(70.50%)
[3]
[4]
[13] array · 5 items
[0]
III–IV
[1]
44(50.57%)
[2]
43(49.43%)
[3]
[4]
locator
section[18]/table-wrap[2]#T3
[5] object · 16 fields
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asset:table:pmid:33282911:4
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jats-table
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The chi-square test of the relation between risk score and clinical features in GSE14520 cohort.
structure object · 5 fields
pmcid
PMC7691640
section_index
18
section_title
Clinical Correlation Analysis of the Prognostic Model
row_count
32
column_count
5
table object · 8 fields
label
TABLE 4
caption
The chi-square test of the relation between risk score and clinical features in GSE14520 cohort.
rows array · 32 items
[0] array · 4 items
[0]
Clinical feature
[1]
Risk score
[2]
c2
[3]
p
[1] array · 5 items
[0]
[1]
High risk n(%)
[2]
Low risk n(%)
[3]
[4]
[2] array · 5 items
[0]
Age
[1]
[2]
[3]
1.162
[4]
0.281
[3] array · 5 items
[0]
>65
[1]
9(47.37%)
[2]
10(52.63%)
[3]
[4]
[4] array · 5 items
[0]
≤65
[1]
119(60.10%)
[2]
79(39.90%)
[3]
[4]
[5] array · 5 items
[0]
Gender
[1]
[2]
[3]
0.39
[4]
0.533
[6] array · 5 items
[0]
MALE
[1]
113(59.79%)
[2]
76(40.21%)
[3]
[4]
[7] array · 5 items
[0]
FEMALE
[1]
15(53.57%)
[2]
13(46.43%)
[3]
[4]
[8] array · 5 items
[0]
ALT
[1]
[2]
[3]
0.666
[4]
0.415
[9] array · 5 items
[0]
>50U/L
[1]
56(62.22%)
[2]
34(37.78%)
[3]
[4]
[10] array · 5 items
[0]
≤50 U/L
[1]
72(56.69%)
[2]
55(43.31%)
[3]
[4]
[11] array · 5 items
[0]
Main Tumor Size
[1]
[2]
[3]
6.126
[4]
0.013
[12] array · 5 items
[0]
>5 cm
[1]
54(70.13%)
[2]
23(29.87%)
[3]
[4]
[13] array · 5 items
[0]
≤5 cm
[1]
74(52.86%)
[2]
66(47.14%)
[3]
[4]
[14] array · 5 items
[0]
Multitumor
[1]
[2]
[3]
1.205
[4]
0.272
[15] array · 5 items
[0]
NO
[1]
97(57.06%)
[2]
73(42.94%)
[3]
[4]
[16] array · 5 items
[0]
YES
[1]
31(65.96%)
[2]
16(34.04%)
[3]
[4]
[17] array · 5 items
[0]
Stage TNM
[1]
[2]
[3]
13.417
[4]
<0.001
[18] array · 5 items
[0]
I–II
[1]
88(52.38%)
[2]
80(47.62%)
[3]
[4]
[19] array · 5 items
[0]
III–IV
[1]
40(81.63%)
[2]
9(18.37%)
[3]
[4]
[20] array · 5 items
[0]
Cirrhosis
[1]
[2]
[3]
11.241
[4]
<0.001
[21] array · 5 items
[0]
YES
[1]
125(60%)
[2]
75(40%)
[3]
[4]
[22] array · 5 items
[0]
NO
[1]
3(17.65%)
[2]
14(82.35%)
[3]
[4]
[23] array · 5 items
[0]
Stage BCLC
[1]
[2]
[3]
[4]
[24] array · 5 items
[0]
0-A
[1]
88(53.33%)
[2]
77(46.67%)
[3]
9.095
[4]
0.003
[25] array · 5 items
[0]
B-C
[1]
40(76.92%)
[2]
12(23.08%)
[3]
[4]
[26] array · 5 items
[0]
CLIP_Score
[1]
[2]
[3]
[4]
[27] array · 5 items
[0]
≥2
[1]
33(68.75%)
[2]
15(31.25%)
[3]
2.429
[4]
0.119
[28] array · 5 items
[0]
<2
[1]
95(56.21%)
[2]
74(43.79%)
[3]
[4]
[29] array · 5 items
[0]
AFP
[1]
[2]
[3]
1.103
[4]
0.294
[30] array · 5 items
[0]
>300 ng/ml
[1]
61(62.89%)
[2]
36(37.11%)
[3]
[4]
[31] array · 5 items
[0]
≥300 ng/ml
[1]
67(55.83)
[2]
53(44.17%)
[3]
[4]
locator
section[18]/table-wrap[3]#T4
gaps array · 2 items
[0]
asset:data:geo:GSE14520 not downloaded
[1]
asset:data:geo:GSE14520 licence not read
analysis object · 4 fields
state
complete
methods array · 2 items
[0] object · 10 fields
id
method-1
family
survival_analysis
specific
cox_proportional_hazards
label
Survival analysis
dsl_operations array · 1 item
[0]
cox_ph
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
score
1
band
verbatim
quote
A LASSO Cox regression prognostic model was developed by combining The Cancer Genome Atlas Liver Hepatocellular Carcinoma (TCGA-LIHC) with the International Cancer Genome Consortium (ICGC) LIRI-JP cohort, and internal (TCGA, ICGC) and external (GSE14520) validation analyses were conducted on the predictive value of the model.
[1] object · 10 fields
id
method-2
family
contingency_analysis
specific
chi_square
label
Categorical (contingency table) analysis
dsl_operations array · 1 item
[0]
chi_square_test
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
categorical_cross_tabulation
evidence object · 3 fields
score
0.7
band
medium
quote
chi-square
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gaps array · 0 items
capability object · 3 fields
state
complete
requirements array · 1 item
[0] object · 6 fields
capability_id
capability:computational_analysis
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Computational analysis platform
assay_families array · 9 items
[0]
meta_analysis
[1]
machine_learning
[2]
survival_analysis
[3]
statistical_regression
[4]
pca
[5]
molecular_docking
[6]
network_analysis
[7]
differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
gaps array · 0 items
readiness object · 8 fields
state
complete
tier
R1
blocked_on
nothing:replicable_now
axes object · 3 fields
method object · 5 fields
tier
R1
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true
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[0]
cox_ph
missing_operations array · 0 items
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards.
capability object · 4 fields
tier
R1
capability_id
capability:computational_analysis
availability_state
owned
basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
R1
reachable
true
accessions array · 1 item
[0]
GSE14520
resolved_accessions array · 1 item
[0]
GSE14520
statements array · 1 item
[0]
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
basis
The paper names GSE14520 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
dsl_operations array · 1 item
[0]
cox_ph
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[0]
source:pmid:33282911
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data:geo:GSE14520
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[5]
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[0]
run_analysis
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data:geo:GSE14520
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partial
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extraction_review
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MiniMax-M3.1-Flash
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minimax
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minimax
read_at
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single_reader
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verbatim
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verbatim
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3
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25530
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784
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extraction
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complete
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MiniMax-M3.1-Flash
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minimax
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review.machine_critique
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review.human_critique
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not_run
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null
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execution.not_run
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pmid:33282911
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paper
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pmid:33282911
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source:pmid:33282911
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PMID 33282911 full text
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data:geo:GSE14520
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GEO GSE14520
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activity-reading-sci-2026-11-01
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classification
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pmid:33282911
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pmid:33282911
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source:pmid:33282911
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PMID 33282911 full text
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data:geo:GSE14520
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GEO GSE14520
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agent:corpus-assay-engine
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activity-read-33282911
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extraction
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source:pmid:33282911
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agent:minimax-reader
[2] object · 4 fields
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activity-resolve-GSE14520
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accession_resolution
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data:geo:GSE14520
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agent:corpus-assay-engine
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agent:corpus-assay-engine
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Corpus assay engine
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agent:minimax-reader
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MiniMax literature reader
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reading-sci-2026-11-01
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2cb3e42f047d2ecf
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pmid:33282911
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null
gaps array · 6 items
[0]
asset:data:geo:GSE14520 licence not read
[1]
asset:data:geo:GSE14520 not downloaded
[2]
execution.not_run
[3]
review.human_critique
[4]
review.independent_reader
[5]
review.machine_critique
assays array · 1 item
[0] object · 11 fields
role
analysis
definition_id
survival_analysis
definition_version
f2132e96ae6c7a4e
required_operations array · 1 item
[0]
cox_ph
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
A LASSO Cox regression prognostic model was developed by combining The Cancer Genome Atlas Liver Hepatocellular Carcinoma (TCGA-LIHC) with the International Cancer Genome Consortium (ICGC) LIRI-JP cohort, and internal (TCGA, ICGC) and external (GSE14520) validation analyses were conducted on the predictive value of the model.
order_basis
analysis_only
id
assay:1
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:33282911", "kind": "science-record", "revision": 6, "content_hash": "sha256:9395717d38b50a2fe4ec56c5df28d7d7bc5e4a78b7c023a7dad9bde4b581736a", "created_at": "2026-11-01T15:41:18Z", "updated_at": "2026-11-01T21:24:14Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "A Prognostic Model of 15 Immune-Related Gene Pairs Associated With Tumor Mutation Burden for Hepatocellular Carcinoma.", "doi": "10.3389/fmolb.2020.581354", "pmid": "33282911", "authors": ["Junyu Huo", "Liqun Wu", "Yunjin Zang"], "journal": "Frontiers in molecular biosciences", "year": 2020, "abstract": "INTRODUCTION: Tumor mutation burden (TMB) is an emerging biomarker for immunotherapy of hepatocellular carcinoma (HCC), but its value for clinical application has not been fully revealed.\nMATERIALS AND METHODS: We used the Wilcox test to identify the differentially expressed immune-related genes (DEIRGs) in groups with high and low TMB as well as screened the immune gene pairs related to prognosis using univariate Cox regression analysis. A LASSO Cox regression prognostic model was developed by combining The Cancer Genome Atlas Liver Hepatocellular Carcinoma (TCGA-LIHC) with the International Cancer Genome Consortium (ICGC) LIRI-JP cohort, and internal (TCGA, ICGC) and external (GSE14520) validation analyses were conducted on the predictive value of the model. We also explored the relationship between the prognostic model and tumor microenvironment via the ESTIMATE algorithm and performed clinical correlation analysis by the chi-square test, revealing its underlying molecular mechanism with the help of Gene Set Enrichment Analysis (GSEA).\nRESULTS: The prognostic model consisting of 15 immune gene pairs showed high predictive value for short- and long-term survival of HCC in three independent cohorts. Based on univariate multivariate Cox regression analysis, the prognostic model could be used to independently predict the prognosis in each independent cohort. The immune score, stromal score, and estimated score values were lower in the high-risk group than in the low-risk group. As shown by the chi-square test, the prognostic model exhibited an obvious correlation with the tumor stage [American Joint Committee on Cancer tumor-node-metastasis (AJCC-TNM) (p < 0.001), Barcelona Clinic Liver Cancer (BCLC) (p = 0.003)], histopathological grade (p = 0.033), vascular invasion (p = 0.009), maximum tumor diameter (p = 0.013), and background of liver cirrhosis (p < 0.001). GSEA revealed that the high-risk group had an enrichment of many oncology features, including the cell cycle, mismatch repair, DNA replication, RNA degradation, etc.\nCONCLUSION: Our research developed and validated a reliable prognostic model associated with TMB for HCC, which may help to further enrich the therapeutic targets of HCC.", "claims": [{"id": "claim-method", "statement": "A LASSO Cox regression prognostic model was developed by combining The Cancer Genome Atlas Liver Hepatocellular Carcinoma (TCGA-LIHC) with the International Cancer Genome Consortium (ICGC) LIRI-JP cohort, and internal (TCGA, ICGC) and external (GSE14520) validation analyses were conducted on the predictive value of the model.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33282911", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "A LASSO Cox regression prognostic model was developed by combining The Cancer Genome Atlas Liver Hepatocellular Carcinoma (TCGA-LIHC) with the International Cancer Genome Consortium (ICGC) LIRI-JP cohort, and internal (TCGA, ICGC) and external (GSE14520) validation analyses were conducted on the predictive value of the model."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33282911", "locator": "sections[23] \"Data Availability Statement\" paragraph 2", "quote": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": null, "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:33282911"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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