Inventor · disambiguated record
Carlos Araya
Also filed as: ARAYA CARLOS · ARAYA CARLOS L · ARAYA CARLOS LUIS
12 granted patents·11 pending applications·85 citations·filing 2009–2023
89Inventor score
Top patents by PatentIndex Score
23 records- 0188US10061573B2User interfaces of application porting software platformMOBILIZE NET CORP·Filed 2015·Granted Aug 28, 2018·14 cites·24 claims
- 0288US10019259B2Code transformation using extensibility librariesMOBILIZE NET CORP·Filed 2015·Granted Jul 10, 2018·11 cites·20 claims
- 0388US9465608B2Code separation with semantic guaranteesARTINSOFT CORP·Filed 2013·Granted Oct 11, 2016·18 cites·28 claims
- 0483US10102108B2Injected instrumentation application monitoring and managementMOBILIZE NET CORP·Filed 2016·Granted Oct 16, 2018·5 cites·25 claims
- 0582US9459862B2Automated porting of application to mobile infrastructuresARTINSOFT CORP·Filed 2014·Granted Oct 4, 2016·11 cites·26 claims
- 0681US9239710B2Programming language transformations with abstract syntax tree extensionsARTINSOFT CORP·Filed 2013·Granted Jan 19, 2016·9 cites·24 claims
- 0776US11798651B2Molecular evidence platform for auditable, continuous optimization of variant interpretation in genetic and genomic testing and analysisINVITAE CORP·Filed 2022·Granted Oct 24, 2023·0 cites·20 claims
- 0875US11462299B2Molecular evidence platform for auditable, continuous optimization of variant interpretation in genetic and genomic testing and analysisINVITAE CORP·Filed 2018·Granted Oct 4, 2022·1 cites·20 claims
- 0974US9213541B2Creation, generation, distribution and application of self-contained modifications to source codeARAYA CARLOS·Filed 2009·Granted Dec 15, 2015·15 cites·24 claims
- 1071US12136472B2Molecular evidence platform for auditable, continuous optimization of variant interpretation in genetic and genomic testing and analysisLABORATORY CORP AMERICA HOLDINGS·Filed 2023·Granted Nov 5, 2024·0 cites·19 claims
- 1171US2023187016A1Systems and methods for the interpretation of genetic and genomic variants via an integrated computational and experimental deep mutational learning frameworkINVITAE CORP·Filed 2022·Application pending·0 cites
- 1266US10886007B2Methods and systems for identification of biomolecule sequence coevolution and applications thereofUNIV LELAND STANFORD JUNIOR·Filed 2016·Granted Jan 5, 2021·1 cites·12 claims
- 1365US2025006313A1High-throughput prediction of variant effects from conformational dynamicsINVITAE CORP·Filed 2022·Application pending·0 cites
- 1459US2019348151A1Systems and Methods for Multi-Scale, Annotation-Independent Detection of Functionally-Diverse Units of Recurrent Genomic AlterationUNIV LELAND STANFORD JUNIOR·Filed 2019·Application pending·0 cites
- 1552US2018365372A1Systems and Methods for the Interpretation of Genetic and Genomic Variants via an Integrated Computational and Experimental Deep Mutational Learning FrameworkJUNGLA INC·Filed 2018·Application pending·0 cites
- 1651US2012079429A1Systems and methods for touch-based media guidanceSTATHACOPOULOS PAUL T·Filed 2011·Application pending·0 cites
- 1750US2016378915A1Systems and Methods for Multi-Scale, Annotation-Independent Detection of Functionally-Diverse Units of Recurrent Genomic AlterationUNIV LELAND STANFORD JUNIOR·Filed 2016·Application pending·0 cites
- 1849US2012078953A1Browsing hierarchies with social recommendationsARAYA CARLOS·Filed 2010·Application pending·0 cites
- 1949US2012078885A1Browsing hierarchies with editorial recommendationsARAYA CARLOS·Filed 2010·Application pending·0 cites
- 2049US2012078952A1Browsing hierarchies with personalized recommendationsARAYA CARLOS·Filed 2010·Application pending·0 cites
- 2149US2012078954A1Browsing hierarchies with sponsored recommendationsARAYA CARLOS·Filed 2010·Application pending·0 cites
- 2234US2021151123A1Interpretation of Genetic and Genomic Variants via an Integrated Computational and Experimental Deep Mutational Learning FrameworkJUNGLA INC·Filed 2018·Application pending·0 cites
- 2332US10360513B2Belief data model management serviceARAYA CARLOS LUIS·Filed 2015·Granted Jul 23, 2019·0 cites·20 claims
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