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Version: 1.0.0 | Published: 8 Oct 2024 | Updated: 274 days ago

Genomics England - Secondary Data - PHE/NCRAS

Dataset

Documentation

Description:
av_patient Patient information - demographics and death details. av_tumour Tumour catalogue and characterisation for all patients with registerable tumour. Table"s anon_tumour_id is used to link treatment tables also available in NCRAS. One row per tumour (av* table specific anon_tumour_id), per participant at the point of registration of that cancer/tumour with NCRAS. av_treatment Tumour linked catalogue of treatments and sites that provided them for all patients with registerable tumour. av_imd The Income Deprivation Domain (IMD table) measures the proportion of the population experiencing deprivation relating to low income. The definition of low income used includes both those people that are out-of-work and those that are in work but who have low earnings. av_rtd Routes to Diagnosis: cancer registration data are combined with Administrative Hospital Episode Statistics data, Cancer Waiting Times data and data from the cancer screening programmes. Using these datasets cancers registered in England which were diagnosed in 2006 to 2016 are categorised into one of eight Routes to Diagnosis. The methodology is described in detail in the British Journal of Cancer article "Routes to Diagnosis for cancer - Determining the patient journey using multiple routine datasets". cwt The National Cancer Waiting Times Monitoring Data Set supports the continued management and monitoring of waiting times. sact Systemic Anti-Cancer Therapy (chemotherapy detail) data for cancer participants from NHSE covering regimens between 04/2012 and 08/2022. One row per chemotherapy cycle, per tumour (SACT-specific anon_tumour_id), per participant. rtds The Radiotherapy Data Set (RTDS) standard (SCCI0111) is an existing standard that has required all NHS Acute Trust providers of radiotherapy services in England to collect and submit standardised data monthly against a nationally defined data set since 2009. The purpose of the standard is to collect consistent and comparable data across all NHS Acute Trust providers of radiotherapy services in England in order to provide intelligence for service planning, commissioning, clinical practice and research and the operational provision of radiotherapy services across England. Data is available from 01/04/2009. The data is linked at a patient level and can be linked to the latest available av_patient table. ncras_did The Diagnostic Imaging Dataset (DID) is a central collection of detailed information about diagnostic imaging tests carried out on NHS patients, extracted from local radiology information systems and submitted monthly. The DID captures information about referral source, details of the test (type of test and body site), demographic information such as GP registered practice, patient postcode, ethnicity, gender and date of birth, plus data items about different events (date of imaging request, date of imaging, date of reporting, which allows calculation of time intervals. lucada_2013 The National Lung Can

Coverage

Typical Age Range:
0-150
Follow Up:
> 10 Years
Pathway:
Secondary care cancer pathways.

Provenance

Temporal

Accrual Periodicity:
Quarterly
Distribution Release Date:
30 March 2023
Start Date:
01 January 1985
End Date:
30 December 2022
Time Lag:
Variable

Accessibility

Access

Access Service:
More information about the Genomics England Research Environment can be found here: https://www.genomicsengland.co.uk/about-genomics-england/research-environment/ https://research-help.genomicsengland.co.uk/display/GERE/1.+The+Genomics+England+Research+Environment Genomics England 100k participants have consented to longitudinal lifetime followup and recontact safely through our clinical network. BRST (Bioinformatics Research Services) are a team of bioinformatics who know the dataset inside out and provide consultancy projects on a case by case basis. Our network of clinical and medical experts can be made available on case by case basis. Researchers have the opportunity to work with our and access the GeCIP network who are a community of world-leading experts in specific cancers and rare diseases.
Access Request Cost:
Fees will be dependent on the type of access that is necessary. Raw data is not eligible for export. Summary-level data may be exported provided that it is approved through the Genomics England Airlock Process
Delivery Lead Time:
Not applicable
Jurisdictions:
GB-GBN
Data Controller:
PUBLIC HEALTH ENGLAND
Data Processor:
GENOMICS ENGLAND

Usage

Resource Creators:
Genomics England

Format and Standards

Vocabulary Encoding Schemes:
  • READ
  • SNOMED CT
  • NHS NATIONAL CODES
  • ICD10
  • OPCS4
  • ODS
Languages:
en
Formats:
Multiple Formats Available

Observations

Statistical Population
Population Description
Population Size
Measured Property
Observation Date
Persons
Cancer Tumour - Number of genomes
-1
Count
01 January 1970
Persons
Rare Disease Participants
-1
Count
01 January 1970
Persons
Cancer Germline - Number of genomes
-1
Count
01 January 1970
Persons
Rare Disease - Number of genomes
-1
Count
01 January 1970
Persons
Cancer Participants
-1
Count
01 January 1970