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Extracting Electronic Health Record (EHR) Data Using Transfer Learning

January 9, 2023 Corey Fournier, Senior Data Engineer 1 Comment

by Corey Fourier, Senior Data Engineer At ThinkGenetic, Inc. our goal is to reduce the time to diagnosis for genetic and rare conditions. Given they are rare, we must be… CONTINUE

Filed Under: Research, Tech Tagged With: algorithms, BERT model, clinical note, EHR, electronic health records, genetic conditino, genetic condition, Google, ICD-10, Medical Coding, medical record, misdiagnosed, Name Entity Recognition, Natural Language Processing, NLP, Procedures codes, Rare Disease, rare genetic disease, Relation Extraction, Semantic Role labeling, Shi and Lin, Snomed, structured data, T5, Text-to-text Transfer Transformers, undiagnosed, unstructured data

Research in Artificial Intelligence for Rare Genetic Diseases

November 11, 2021 Sarika Kondra Leave a Comment

The number of AI-based research publications on rare diseases from 2010-2019.

There are over 7000 rare genetic disorders (RGD) and only 5% of them have FDA approved treatments. Though the number of RGDs is high, they are heterogenous and geographically disparate…. CONTINUE

Filed Under: Tech Tagged With: artificial intelligence, rare genetic disease, research, Sarika Kondra

Taking a Closer Look at Advocacy – The TSC Alliance®: Hope No Matter How Complex

October 7, 2021 Jessica Dronen, MS, CGC Leave a Comment

ThinkGenetic is honored to partner with many incredible organizations, each with their own stories, struggles and triumphs. This month, we are taking a moment to highlight the work and rebranding… CONTINUE

Filed Under: Advocacy, Partners Tagged With: Dawn Laney, Educator Mentor Program, Jessica Dronen, rare genetic disease, TS Alliance, TSC, TSC Alliance, TSC clinics, Tuberous sclerosis, Tuberous sclerosis complex, tumors

Genetic Condition Update for 06/02/2017

June 2, 2017 thinkgenetic Leave a Comment

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to anyone searching for answers on genetic diseases and… CONTINUE

Filed Under: Updates Tagged With: adenosine triphosphate, ATP, bones, brittle bone disease, creatine, dienoyl coa, dienoyl-coa reductase deficiency, fracture bones, GAMT, GAMT gene, genetic neurological disorder, Guanidinoacetate methyltransferase deficiency, neurologic disorder, OI, osteogenesis imperfecta, ovarian failure, Rare Disease, rare disorder, rare genetic disease, turner syndrome

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