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pmid:32580137

Molecular analysis of Chinese oesophageal squamous cell carcinoma identifies novel subtypes associated with distinct clinical outcomes.

Meng Liu · Haiyin An · Yuan Zhang · Wei Sun · Shujun Cheng · Ruozheng Wang · Xiyan Wang · Lin Feng

EBioMedicine · 2020 doi:10.1016/j.ebiom.2020.102831

Paper

complete

Experiment

complete

Data

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Analysis

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Execution

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title
Molecular analysis of Chinese oesophageal squamous cell carcinoma identifies novel subtypes associated with distinct clinical outcomes.
doi
10.1016/j.ebiom.2020.102831
pmid
32580137
authors array · 8 items
[0]
Meng Liu
[1]
Haiyin An
[2]
Yuan Zhang
[3]
Wei Sun
[4]
Shujun Cheng
[5]
Ruozheng Wang
[6]
Xiyan Wang
[7]
Lin Feng
journal
EBioMedicine
year
2020
abstract
BACKGROUND: Oesophageal squamous cell carcinoma (ESCC) is a highly heterogeneous cancer with a distinct incidence and prognosis. Molecular events driving ESCC subtypes and prognosis have not been established, and little is known regarding Chinese ESCC patients in Xinjiang, China. METHODS: Here, we first integrated the genomic and transcriptomic data of 125 Chinese ESCC patients from Xinjiang Tumor Hospital (Urumqi, China). Two independent datasets of GSE53624 and The Cancer Genome Atlas (TCGA) ESCC were used to confirm the results of this study. DNA mutation and overall survival (OS) were analysed independently in the Chinese ESCC cohorts. FINDINGS: Genomic analyses revealed a consistent mutation signatures and discordance among mutated genes across the different ESCC cohorts. In addition, transcriptomic profiling identified three Chinese ESCC subtypes associated with clinical and molecular attributes, including patient survival, lymph node status and genetic profile. Moreover, Chinese ESCC subtypes have distinct metabolic, inflammatory, metastatic, and cell proliferation features and unique potential therapeutics. Furthermore, the expression of cell cycle- and/or cell proliferation-related genes was higher in cyclin D1 (CCND1)-amplified tumours than in CCND1-normal tumours from Chinese ESCC patients, suggesting that CCND1 amplification promoted cell proliferation. INTERPRETATION: Our findings provide a framework to facilitate the rational categorization of ESCC in Chinese patients and a foundation for new therapies. FUNDING: This study was supported by the Research Fund of Key Laboratory of Xinjiang oncology (Grant no.2017D04006) and the Outstanding Youth Science and technology training project fund of Xinjiang, China (Grant no. 2017Q058).
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Spearman's correlation coefficients and adjusted P values were calculated for all CNA-mRNA pairs for 23,109 genes (Supplementary Data 11).
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sections[15] "Identification of copy-number alterations (CNAs) associated with mRNA abundance among the Chinese ESCC subtypes" paragraph 2
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Spearman's correlation coefficients and adjusted P values were calculated for all CNA-mRNA pairs for 23,109 genes (Supplementary Data 11).
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Genomic and transcriptomic data have been uploaded to the Genome Sequence Archive of Beijing Institute of Genomics, Chinese Academy of Sciences (http://gsa.big.as.cn/) under accession number HRA000178. Data that support the findings of this study are available from the TCGA (http://cancergenome.nib.gov) and GEO databases (http://www.ncbi.nlm.nih.gov/geo).
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Genomic and transcriptomic data have been uploaded to the Genome Sequence Archive of Beijing Institute of Genomics, Chinese Academy of Sciences (http://gsa.big.as.cn/) under accession number HRA000178. Data that support the findings of this study are available from the TCGA (http://cancergenome.nib.gov) and GEO databases (http://www.ncbi.nlm.nih.gov/geo).
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Genomic and transcriptomic data have been uploaded to the Genome Sequence Archive of Beijing Institute of Genomics, Chinese Academy of Sciences (http://gsa.big.as.cn/) under accession number HRA000178. Data that support the findings of this study are available from the TCGA (http://cancergenome.nib.gov) and GEO databases (http://www.ncbi.nlm.nih.gov/geo).
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title
LncRNA profile study reveals a three-lncRNA signature associated with the survival of esophageal squamous cell carcinoma patients (original)
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Clinical characteristics of patients with ESCC in discovery cohorts and validation cohorts.
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Clinical and molecular relevance of the Chinese ESCC subtypes
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Table 1
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Clinical characteristics of patients with ESCC in discovery cohorts and validation cohorts.
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Characteristics
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[3]
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15 (29.4%)
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2 (6.1%)
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21 (17.6%)
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51(42.9%)
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33(27.7%)
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19 (37.3%)
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39 (32.8%)
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[6]
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[7]
32 (62.7%)
[8]
26 (78.8%)
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80 (67.2%)
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[3]
31 (68.9%)
[4]
96 (76.8%)
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[6]
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27 (52.9%)
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5 (15.2%)
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45 (37.8%)
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[7]
24 (47.1%)
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28 (84.8%)
[9]
74 (62.2%)
[17] array · 10 items
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[5]
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[8]
[9]
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[1]
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[2]
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[3]
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[5]
[6]
6 (17.1%)
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4 (7.8%)
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4 (12.1%)
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14 (11.8%)
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30 (66.7%)
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[6]
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33 (64.7%)
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17 (51.5%)
[9]
69 (58.0%)
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[6]
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[7]
14 (27.5%)
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12 (36.4%)
[9]
36 (30.3%)
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[6]
7 (20.0%)
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10 (19.6%)
[8]
6 (18.2%)
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23 (19.3%)
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[0]
G2
[1]
31 (63.3%)
[2]
16 (53.3%)
[3]
26 (57.8%)
[4]
73 (58.9%)
[5]
[6]
20 (57.1%)
[7]
25 (49.0%)
[8]
19 (57.6%)
[9]
64 (53.8%)
[24] array · 10 items
[0]
G3
[1]
7 (14.3%)
[2]
12 (40.0%)
[3]
9 (20.0%)
[4]
28 (22.6%)
[5]
[6]
8 (22.9%)
[7]
16 (31.4%)
[8]
8 (24.2%)
[9]
32 (26.9%)
[25] array · 10 items
[0]
T stage
[1]
[2]
[3]
[4]
[5]
0.374
[6]
[7]
[8]
[9]
[26] array · 10 items
[0]
T1
[1]
2 (4.1%)
[2]
0 (0.0%)
[3]
1 (2.2%)
[4]
3 (2.4%)
[5]
[6]
6 (17.1%)
[7]
1 (2.0%)
[8]
1 (3.0%)
[9]
8 (6.7%)
[27] array · 10 items
[0]
T2
[1]
9 (18.4%)
[2]
2 (6.5%)
[3]
8 (17.8%)
[4]
19 (15.2%)
[5]
[6]
5 (14.3%)
[7]
8 (15.7%)
[8]
7 (21.2%)
[9]
20 (16.8%)
[28] array · 10 items
[0]
T3
[1]
33 (67.3%)
[2]
28 (90.3%)
[3]
31 (68.9%)
[4]
92 (73.6%)
[5]
[6]
18 (51.4%)
[7]
29 (56.9%)
[8]
15 (45.5%)
[9]
62 (52.1%)
[29] array · 10 items
[0]
T4
[1]
5 (10.2%)
[2]
1 (3.2%)
[3]
5 (11.1%)
[4]
11 (8.8%)
[5]
[6]
6 (17.1%)
[7]
13 (25.5%)
[8]
10 (30.3%)
[9]
29 (24.4%)
[30] array · 10 items
[0]
N stage
[1]
[2]
[3]
[4]
[5]
0.054
[6]
[7]
[8]
[9]
[31] array · 10 items
[0]
N0
[1]
26 (53.1%)
[2]
10 (32.3%)
[3]
13 (28.9%)
[4]
49 (39.2%)
[5]
[6]
17 (48.6%)
[7]
22 (43.1%)
[8]
15 (45.5%)
[9]
54 (45.4%)
[32] array · 10 items
[0]
N1
[1]
10 (20.4%)
[2]
15 (48.4%)
[3]
20 (44.4%)
[4]
45 (36.0%)
[5]
[6]
12 (34.3%)
[7]
16 (31.4%)
[8]
14 (42.4%)
[9]
42 (35.3%)
[33] array · 10 items
[0]
N2
[1]
9 (18.4%)
[2]
4 (12.9%)
[3]
11 (24.4%)
[4]
24 (19.2%)
[5]
[6]
3 (8.6%)
[7]
8 (15.7%)
[8]
2 (6.1%)
[9]
13 (10.9%)
[34] array · 10 items
[0]
N3
[1]
4 (8.2%)
[2]
2 (6.5%)
[3]
1 (2.2%)
[4]
7 (5.6%)
[5]
[6]
3 (8.6%)
[7]
5 (9.8%)
[8]
2 (6.1%)
[9]
10 (8.4%)
[35] array · 10 items
[0]
TNM stage
[1]
[2]
[3]
[4]
[5]
0.121
[6]
[7]
[8]
[9]
[36] array · 10 items
[0]
I-II
[1]
25 (51.0%)
[2]
11 (35.5%)
[3]
14 (31.1%)
[4]
50 (40.0%)
[5]
[6]
20 (57.1%)
[7]
19 (37.3%)
[8]
14 (42.4%)
[9]
53 (44.5%)
[37] array · 10 items
[0]
III-IV
[1]
24 (49.0%)
[2]
20 (64.5%)
[3]
31 (68.9%)
[4]
75 (60.0%)
[5]
[6]
15 (42.9%)
[7]
32 (62.7%)
[8]
19 (57.6%)
[9]
66 (55.5%)
[38] array · 10 items
[0]
Lymph Node status
[1]
[2]
[3]
[4]
[5]
0.037
[6]
[7]
[8]
[9]
[39] array · 10 items
[0]
N0
[1]
26 (53.1%)
[2]
10 (32.3%)
[3]
13 (28.9%)
[4]
49 (39.2%)
[5]
[6]
17 (48.6%)
[7]
22 (43.1%)
[8]
15 (45.5%)
[9]
54 (45.4%)
[40] array · 10 items
[0]
N1,2,3
[1]
23 (46.9%)
[2]
21 (67.7%)
[3]
32 (71.1%)
[4]
76 (60.8%)
[5]
[6]
18 (51.4%)
[7]
29 (56.9%)
[8]
18 (54.5%)
[9]
65 (54.6%)
[41] array · 10 items
[0]
Survival, months
[1]
[2]
[3]
[4]
[5]
0.012b
[6]
[7]
[8]
[9]
[42] array · 10 items
[0]
Median
[1]
34.4
[2]
22.6
[3]
16.5
[4]
26.3
[5]
[6]
61.0
[7]
22.7
[8]
19.2
[9]
32.2
[43] array · 10 items
[0]
Range
[1]
6.7–73.9
[2]
5.7–87.3
[3]
1.7–73.8
[4]
1.7–87.3
[5]
[6]
5.8–72.5
[7]
0.1–72.1
[8]
1.4–72.6
[9]
0.1–72.6
locator
section[21]/table-wrap[1]#tbl0001
gaps array · 2 items
[0]
asset:data:geo:GSE53624 not downloaded
[1]
asset:data:geo:GSE53624 licence not read
analysis object · 4 fields
state
partial
methods array · 6 items
[0] object · 10 fields
id
method-1
family
correlation_analysis
specific
spearman
label
Correlation analysis
dsl_operations array · 1 item
[0]
spearman_rho
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
paired_numeric_columns
evidence object · 3 fields
score
1
band
verbatim
quote
Spearman's correlation coefficients and adjusted P values were calculated for all CNA-mRNA pairs for 23,109 genes (Supplementary Data 11).
[1] object · 10 fields
id
method-2
family
group_comparison
specific
wilcoxon
label
Group comparison
dsl_operations array · 0 items
missing_operations array · 1 item
[0]
group_comparison_wilcoxon
expressible
false
parameters object · 0 fields
data_shapes array · 1 item
[0]
two_or_more_groups_continuous
evidence object · 3 fields
score
0.8
band
high
quote
Wilcoxon
[2] object · 10 fields
id
method-3
family
survival_analysis
specific
kaplan_meier
label
Survival analysis
dsl_operations array · 1 item
[0]
survival_km
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
0.8
band
high
quote
Kaplan-Meier
[3] object · 10 fields
id
method-4
family
survival_analysis
specific
log_rank_test
label
Survival analysis
dsl_operations array · 1 item
[0]
logrank_test
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
0.8
band
high
quote
log-rank
[4] object · 10 fields
id
method-5
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
0.8
band
high
quote
chi-square
[5] object · 10 fields
id
method-6
family
contingency_analysis
specific
fisher_exact
label
Categorical (contingency table) analysis
dsl_operations array · 2 items
[0]
contingency_table
[1]
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
0.8
band
high
quote
Fisher's exact
targets array · 0 items
gaps array · 1 item
[0]
method.reader_differs_from_extractor
capability object · 3 fields
state
complete
requirements array · 1 item
[0] object · 6 fields
capability_id
capability:computational_analysis
label
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
expressible
true
required_operations array · 1 item
[0]
spearman_rho
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: spearman.
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]
GSE53624
resolved_accessions array · 1 item
[0]
GSE53624
statements array · 1 item
[0]
Genomic and transcriptomic data have been uploaded to the Genome Sequence Archive of Beijing Institute of Genomics, Chinese Academy of Sciences (http://gsa.big.as.cn/) under accession number HRA000178. Data that support the findings of this study are available from the TCGA (http://cancergenome.nib.gov) and GEO databases (http://www.ncbi.nlm.nih.gov/geo).
basis
The paper names GSE53624 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]
spearman_rho
assets array · 3 items
[0]
source:pmid:32580137
[1]
data:geo:GSE53624
[2]
asset:table:pmid:32580137:1
steps array · 1 item
[0]
run_analysis
must_build object · 5 fields
dsl_operations array · 0 items
converters array · 0 items
readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:GSE53624
gaps array · 0 items
review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-10-31T18:20:48Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
3
usage object · 3 fields
prompt_tokens
34913
completion_tokens
1699
cached_tokens
11784
stages array · 1 item
[0] object · 4 fields
id
extraction
state
complete
reader
MiniMax-M3.1-Flash
provider
minimax
gaps array · 3 items
[0]
review.independent_reader
[1]
review.machine_critique
[2]
review.human_critique
execution object · 5 fields
state
absent
status
not_run
mode
null
runs array · 0 items
gaps array · 1 item
[0]
execution.not_run
provenance object · 7 fields
entities array · 3 items
[0] object · 3 fields
id
pmid:32580137
type
paper
label
pmid:32580137
[1] object · 3 fields
id
source:pmid:32580137
type
manuscript
label
PMID 32580137 full text
[2] object · 3 fields
id
data:geo:GSE53624
type
dataset
label
GEO GSE53624
activities array · 3 items
[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
used array · 3 items
[0] object · 3 fields
id
pmid:32580137
type
paper
label
pmid:32580137
[1] object · 3 fields
id
source:pmid:32580137
type
manuscript
label
PMID 32580137 full text
[2] object · 3 fields
id
data:geo:GSE53624
type
dataset
label
GEO GSE53624
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-32580137
type
extraction
used array · 1 item
[0]
source:pmid:32580137
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE53624
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE53624
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
type
software
label
Corpus assay engine
[1] object · 3 fields
id
agent:minimax-reader
type
software
label
MiniMax literature reader
source_run_id
reading-sci-2026-11-01
dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
2cb3e42f047d2ecf
snapshot_id
ba34b49490d9bfaf
lineage object · 4 fields
parent_id
pmid:32580137
parent_hash
sha256:a9ae800807c4e2fcc52c43538aced77cfbbe4fef080ae6e0d8e61d155425ba9d
fork_of
null
gaps array · 7 items
[0]
asset:data:geo:GSE53624 licence not read
[1]
asset:data:geo:GSE53624 not downloaded
[2]
execution.not_run
[3]
method.reader_differs_from_extractor
[4]
review.human_critique
[5]
review.independent_reader
[6]
review.machine_critique
assays array · 1 item
[0] object · 11 fields
role
analysis
definition_id
correlation_analysis
definition_version
f2132e96ae6c7a4e
required_operations array · 1 item
[0]
spearman_rho
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
Spearman's correlation coefficients and adjusted P values were calculated for all CNA-mRNA pairs for 23,109 genes (Supplementary Data 11).
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:32580137", "kind": "science-record", "revision": 7, "content_hash": "sha256:10151d90023d8a97e52027064d3c5cae545179ef195b7ae7ae44b148520e0ba3", "created_at": "2026-11-01T15:41:04Z", "updated_at": "2026-11-01T22:01:47Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Molecular analysis of Chinese oesophageal squamous cell carcinoma identifies novel subtypes associated with distinct clinical outcomes.", "doi": "10.1016/j.ebiom.2020.102831", "pmid": "32580137", "authors": ["Meng Liu", "Haiyin An", "Yuan Zhang", "Wei Sun", "Shujun Cheng", "Ruozheng Wang", "Xiyan Wang", "Lin Feng"], "journal": "EBioMedicine", "year": 2020, "abstract": "BACKGROUND: Oesophageal squamous cell carcinoma (ESCC) is a highly heterogeneous cancer with a distinct incidence and prognosis. Molecular events driving ESCC subtypes and prognosis have not been established, and little is known regarding Chinese ESCC patients in Xinjiang, China.\nMETHODS: Here, we first integrated the genomic and transcriptomic data of 125 Chinese ESCC patients from Xinjiang Tumor Hospital (Urumqi, China). Two independent datasets of GSE53624 and The Cancer Genome Atlas (TCGA) ESCC were used to confirm the results of this study. DNA mutation and overall survival (OS) were analysed independently in the Chinese ESCC cohorts.\nFINDINGS: Genomic analyses revealed a consistent mutation signatures and discordance among mutated genes across the different ESCC cohorts. In addition, transcriptomic profiling identified three Chinese ESCC subtypes associated with clinical and molecular attributes, including patient survival, lymph node status and genetic profile. Moreover, Chinese ESCC subtypes have distinct metabolic, inflammatory, metastatic, and cell proliferation features and unique potential therapeutics. Furthermore, the expression of cell cycle- and/or cell proliferation-related genes was higher in cyclin D1 (CCND1)-amplified tumours than in CCND1-normal tumours from Chinese ESCC patients, suggesting that CCND1 amplification promoted cell proliferation.\nINTERPRETATION: Our findings provide a framework to facilitate the rational categorization of ESCC in Chinese patients and a foundation for new therapies.\nFUNDING: This study was supported by the Research Fund of Key Laboratory of Xinjiang oncology (Grant no.2017D04006) and the Outstanding Youth Science and technology training project fund of Xinjiang, China (Grant no. 2017Q058).", "claims": [{"id": "claim-method", "statement": "Spearman's correlation coefficients and adjusted P values were calculated for all CNA-mRNA pairs for 23,109 genes (Supplementary Data 11).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:32580137", "locator": "sections[15] \"Identification of copy-number alterations (CNAs) associated with mRNA abundance among the Chinese ESCC subtypes\" paragraph 2", "quote": "Spearman's correlation coefficients and adjusted P values were calculated for all CNA-mRNA pairs for 23,109 genes (Supplementary Data 11)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Genomic and transcriptomic data have been uploaded to the Genome Sequence Archive of Beijing Institute of Genomics, Chinese Academy of Sciences (http://gsa.big.as.cn/) under accession number HRA000178. Data that support the findings of this study are available from the TCGA (http://cancergenome.nib.gov) and GEO databases (http://www.ncbi.nlm.nih.gov/geo).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:32580137", "locator": "sections[17] \"Data availability\" paragraph 2", "quote": "Genomic and transcriptomic data have been uploaded to the Genome Sequence Archive of Beijing Institute of Genomics, Chinese Academy of Sciences (http://gsa.big.as.cn/) under accession number HRA000178. Data that support the findings of this study are available from the TCGA (http://cancergenome.nib.gov) and GEO databases (http://www.ncbi.nlm.nih.gov/geo)."}], "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:32580137"], "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. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE53624"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE53624"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:32580137", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1016/j.ebiom.2020.102831", "sha256": "sha256:5dbbf7f358eb3cf5fc1598b7480ed40e56b9ce3220bb5d06e4c4781ef98b5022", "bytes": 46076, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1016/j.ebiom.2020.102831", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC7317223", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE53624", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE53624", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE53624", "version": null, "note": "Genomic and transcriptomic data have been uploaded to the Genome Sequence Archive of Beijing Institute of Genomics, Chinese Academy of Sciences (http://gsa.big.as.cn/) under accession number HRA000178. 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