Mendelian

@mendelian
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Fixing Diagnosis for Rare Diseases

We have just updated our portal. You can learn a bit more about the changes in this "test" page:
https://storage.googleapis.com/rarediseases/latest.html

#mendelian #raredisease #diagnosis #search

Latest developments in Mendelian. Rare diases diagnosis made easy

We have been thinking about writing a bit about our history how we became a rare disease company, and we made this small draft...

https://raredisease.s3.eu-west-2.amazonaws.com/blog.html

Do you find it insteresting? Should it be included in our main site?

#rarediseases #mendelian #draft #aboutme

The development of a rare disease search tool. A draft of our history

Computer-assisted initial diagnosis of rare diseases

Introduction. Most documented rare diseases have genetic origin. Because of their low individual frequency, an initial diagnosis based on phenotypic symptoms is not always easy, as practitioners might never have been exposed to patients suffering from the relevant disease. It is thus important to develop tools that facilitate symptom-based initial diagnosis of rare diseases by clinicians. In this work we aimed at developing a computational approach to aid in that initial diagnosis. We also aimed at implementing this approach in a user friendly web prototype. We call this tool Rare Disease Discovery. Finally, we also aimed at testing the performance of the prototype. Methods. Rare Disease Discovery uses the publicly available ORPHANET data set of association between rare diseases and their symptoms to automatically predict the most likely rare diseases based on a patient’s symptoms. We apply the method to retrospectively diagnose a cohort of 187 rare disease patients with confirmed diagnosis. Subsequently we test the precision, sensitivity, and global performance of the system under different scenarios by running large scale Monte Carlo simulations. All settings account for situations where absent and/or unrelated symptoms are considered in the diagnosis. Results. We find that this expert system has high diagnostic precision (≥80%) and sensitivity (≥99%), and is robust to both absent and unrelated symptoms. Discussion. The Rare Disease Discovery prediction engine appears to provide a fast and robust method for initial assisted differential diagnosis of rare diseases. We coupled this engine with a user-friendly web interface and it can be freely accessed at http://disease-discovery.udl.cat/. The code and most current database for the whole project can be downloaded from https://github.com/Wrrzag/DiseaseDiscovery/tree/no_classifiers.

Starting to use workable!

https://mendelian.workable.com/ it will be our final solution for recruiting in the rare disease field?

#rarediseases #diagnosis #health |technology

Current Openings - Mendelian

Browse current career opportunities and apply online for jobs at Mendelian

We have been awarded the most innovative business project in the field of new technologies:

https://cincodias.elpais.com/cincodias/2018/06/18/fortunas/1529354433_999546.html

#health #innovation #genetics #tech #spain #rarediseases

Women’secret, Mendelian y New Food, los más innovadores del año

La undécima edición de los galardones del decano de la prensa económica reconoce iniciativas punteras Los galardones se entregan el día 5 de julio en el auditorio de Repsol en Madrid

We have been named in the news, as one of our founders was 😍 interviewed on the upcoming innovations in healthcare.

https://www.himssinsights.eu/data-projects-boost-precision-medicine-spain

#mastodon #introduction #programming #health #genetics #data #london #spain

Data projects boost precision medicine in Spain

Precision medicine is giving birth to leading Spanish-based projects that use big data to speed up rare diseases diagnosis

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By the way... we have just realeased an amazing new test for undiagnosed rare disease patients. Check it out:

https://bit.ly/2KhFzL1

#rarediseases #privacy #introduction #genetics👌

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