PatientMatcher: A customizable Python‐based open‐source tool for matching undiagnosed rare disease patients via the Matchmaker Exchange network. Issue 6 (7th March 2022)
- Record Type:
- Journal Article
- Title:
- PatientMatcher: A customizable Python‐based open‐source tool for matching undiagnosed rare disease patients via the Matchmaker Exchange network. Issue 6 (7th March 2022)
- Main Title:
- PatientMatcher: A customizable Python‐based open‐source tool for matching undiagnosed rare disease patients via the Matchmaker Exchange network
- Authors:
- Rasi, Chiara
Nilsson, Daniel
Magnusson, Måns
Lesko, Nicole
Lagerstedt‐Robinson, Kristina
Wedell, Anna
Lindstrand, Anna
Wirta, Valtteri
Stranneheim, Henrik - Other Names:
- Boycott Kym guestEditor.
Hamosh Ada guestEditor.
Rehm Heidi guestEditor. - Abstract:
- Abstract: The amount of data available from genomic medicine has revolutionized the approach to identify the determinants underlying many rare diseases. The task of confirming a genotype–phenotype causality for a patient affected with a rare genetic disease is often challenging. In this context, the establishment of the Matchmaker Exchange (MME) network has assumed a pivotal role in bridging heterogeneous patient information stored on different medical and research servers. MME has made it possible to solve rare disease cases by "matching" the genotypic and phenotypic characteristics of a patient of interest with patient data available at other clinical facilities participating in the network. Here, we present PatientMatcher (https://github.com/Clinical-Genomics/patientMatcher ), an open‐source Python and MongoDB‐based software solution developed by Clinical Genomics facility at the Science for Life Laboratory in Stockholm. PatientMatcher is designed as a standalone MME server, but can easily communicate via REST API with external applications managing genetic analyses and patient data. The MME node is being implemented in clinical routine in collaboration with the Genomic Medicine Center Karolinska at the Karolinska University Hospital. PatientMatcher is written to implement the MME API and provides several customizable settings, including a custom‐fit similarity score algorithm and adjustable matching results notifications.
- Is Part Of:
- Human mutation. Volume 43:Issue 6(2022)
- Journal:
- Human mutation
- Issue:
- Volume 43:Issue 6(2022)
- Issue Display:
- Volume 43, Issue 6 (2022)
- Year:
- 2022
- Volume:
- 43
- Issue:
- 6
- Issue Sort Value:
- 2022-0043-0006-0000
- Page Start:
- 708
- Page End:
- 716
- Publication Date:
- 2022-03-07
- Subjects:
- gene discovery -- genomic API -- Matchmaker Exchange -- matchmaking -- rare disease
Human chromosome abnormalities -- Periodicals
Mutation (Biology) -- Periodicals
616.04205 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-1004 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/humu.24358 ↗
- Languages:
- English
- ISSNs:
- 1059-7794
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4336.217000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21564.xml