5,000 construction goals
The specifications target 2,000 cases of lung cancer, 1,000 cases of enteric, gastrogen and pancreas cancer; all cases of positive tumours, with other cancers not being used to offset them.

The project establishes a full-text medical record, image, pathology, tissue and end-of-life evidence chain. Specific sources, ranges, quality stratifications and delivery boundaries are confirmed by authorization, data dictionary and acceptance programs.
Priority is given to continuous time, original evidence and cross-modular linkages, rather than simply aggregating isolated tables, images or text.
The specifications target 2,000 cases of lung cancer, 1,000 cases of enteric, gastrogen and pancreas cancer; all cases of positive tumours, with other cancers not being used to offset them.
Priority coverage has been given to the last five years, with the minimum effective time series of not less than three years in principle and containing at least a diagnosis/baseline, treatment and follow-up to multiple nodes.
(c) Establishing traceability relationships with anonymous patient ID, consultations, examinations, sequences, specimens and group samples, and retaining the mosaics of original structures.
(c) Use border design according to de-marking, source clearance, authorized materials and project data; no hospitals, patients or identifiable information are made available.
From traceable leads prior to diagnosis to pathological diagnosis, treatment process and end-of-life visits, the object can be verified by time and by connection keys.
Priority is given to the incorporation of pre-diagnostic historical images and related reports; where there is a “comparison to the front film”, the back-image chain is created using the status tag.
Retain diagnostic basis, baseline T/N/M and Stace; distinguish between available cTNM/pTTNM, date of instalment, source and version.
The sequence of events surrounding the complete medical history, medical instructions, surgery/operation, examination, CT/MRI and pathological documentation of the treatment period.
Recurrence, progress/transfer, death, prolonged non-recurrence and final follow-up visits require time to be supported by original records without any missing extrapolation.
Specific availability is confirmed by data source permission, patient authorization/ethical material, project dictionary and batch acceptance.
| データ域 | Build Requirements and Related Objects | Research and engineering work for the future |
|---|---|---|
| Textbooks and structured events | Outpatients, hospitalization, admission/de-patientization, first course, course of illness, consultation, surgery, diagnosis, testing, medication and medical advice; full_text as original, key records are not cut off. | (c) Re-routing of patients, structuring of clinical texts, temporal sensory signs, queue definition and clinical process analysis. |
| CT/MRI and Image Report | Complete “diagnostic observations” as seen in the “inspection”, dates of examination, date of examination, date of examination, segment, period, layer; DICOM body according priority to authorization and availability. | Image time series research, image-reporting consistency verification, queue screening and multi-modular method validation. |
| Pathology, WSI and IHC | Full pathology report, specimen ID, date of extraction, specimen type, tissue and available tumor/normal properties; H& E WSI and IHC original objects confirmed by project. | Pathology - clinical linkages, blood of sample level data, proof of image methods and preparation for multiscale studies. |
| WES/WGSおよびバルクRNA | Priority FASTQ; at least reusable BAM/CRAM, VCF or expression, QC, reference version and sample metadata, clearly distinguishing between raw data and analytical results, if not available. | (b) Corporate data governance, sample linkages, cross-modular characterization studies and methodological assessments. |
| Follow-up visits, outcome and list of documents | Date of follow-up, re-entry/progress/transfer basis, last follow-up status and file_manifest; PDF, DICOM, WSI, group documents to patients and clinical clients. | Research end-of-service construction, retroactive delivery, data blood audits and quality reviews. |
Project acceptance design is co-formed with associated integrity, clinical text, time sequence logic, video/pathological metadata and batch reports.
Anonymized patients are identified by cross-checking the ID, consultation, examination, sequence, specimen and group samples with primary external keys and list fields to identify isolated objects and the wrong spell.
Full_text integrity is the core of the acceptance and inspection; the coverage and format of the records, time fields, diagnostics, tests, drugs and follow-up fields is verified.
Checking admission, examination, pathology, surgery, medical advice and follow-up time; maintaining evidence chain for comparison, re-phase and ending records of images.
The quality threshold is implemented by project programme based on recommendations for data dictionary, rules check and manual sample output coverage, missing, abnormal, downgraded or eliminated.
Support for data preparation, methodological development, research validation and quality assessment; clinical applications still need to be independently validated by qualified institutions and professionals.
Provide a project-level data readiness framework for time perception modelling, text-structured integration, image-pathological-group linkages and model assessment.
The time-based retroactive basis is maintained by target population, index events, observation windows, exposure, end-of-life and quality door-control organization research queues.
Support for inter-team auditable synergies based on data dictionary, field mapping, humanist, self-quality self-check and batch reports.
The resources below are used to illustrate the principles of the design of the topic and do not represent the resources that have been accessed, owned or distributed.
Discussion with data experts on target cancer species, observation windows, research issues, data mosaics, de-labelling requirements, quality rules and project delivery boundaries, and access to data catalogues and acceptance recommendations for adaptation missions.
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