Inventor · disambiguated record
Brian K. Rhees
Also filed as: RHEES BRIAN K · RHEES BRIAN KENT · RHEES Brian
18 granted patents·12 pending applications·230 citations·filing 2005–2023
94Inventor score
Files withVERINATA HEALTH INC13RAVA RICHARD P11COOPERSURGICAL INC4ECHELON DIAGNOSTICS INC1FAHAM MALEK1
Top patents by PatentIndex Score
30 records- 0198US10388403B2Analyzing copy number variation in the detection of cancerRAVA RICHARD P·Filed 2012·Granted Aug 20, 2019·85 cites·37 claims
- 0297US9260745B2Detecting and classifying copy number variationRAVA RICHARD P·Filed 2012·Granted Feb 16, 2016·62 cites·46 claims
- 0395US10415089B2Detecting and classifying copy number variationVERINATA HEALTH INC·Filed 2015·Granted Sep 17, 2019·14 cites·26 claims
- 0495US9447453B2Resolving genome fractions using polymorphism countsRAVA RICHARD P·Filed 2012·Granted Sep 20, 2016·21 cites·39 claims
- 0592US11884975B2Sequencing methods and compositions for prenatal diagnosesVERINATA HEALTH INC·Filed 2021·Granted Jan 30, 2024·2 cites·10 claims
- 0692US10482993B2Analyzing copy number variation in the detection of cancerVERINATA HEALTH INC·Filed 2016·Granted Nov 19, 2019·11 cites·29 claims
- 0792US9657342B2Sequencing methods for prenatal diagnosesRAVA RICHARD P·Filed 2010·Granted May 23, 2017·14 cites·27 claims
- 0891US10941442B2Sequencing methods and compositions for prenatal diagnosesVERINATA HEALTH INC·Filed 2017·Granted Mar 9, 2021·5 cites·6 claims
- 0991US8700341B2Partition defined detection methodsRAVA RICHARD P·Filed 2011·Granted Apr 15, 2014·14 cites·32 claims
- 1082US9115401B2Partition defined detection methodsVERINATA HEALTH INC·Filed 2014·Granted Aug 25, 2015·1 cites·47 claims
- 1181US10658070B2Resolving genome fractions using polymorphism countsVERINATA HEALTH INC·Filed 2016·Granted May 19, 2020·1 cites·21 claims
- 1278US2022228197A1Method for determining copy number variationsVERINATA HEALTH INC·Filed 2022·Application pending·0 cites
- 1373US11697846B2Detecting and classifying copy number variationVERINATA HEALTH INC·Filed 2019·Granted Jul 11, 2023·0 cites·19 claims
- 1473US2020251180A1Resolving genome fractions using polymorphism countsVERINATA HEALTH INC·Filed 2020·Application pending·0 cites
- 1573US2024203601A1Analyzing copy number variation in the detection of cancerVERINATA HEALTH INC·Filed 2023·Application pending·0 cites
- 1671US11286520B2Method for determining copy number variationsVERINATA HEALTH INC·Filed 2017·Granted Mar 29, 2022·0 cites·21 claims
- 1771US2012149582A1Method for determining copy number variationsRAVA RICHARD P·Filed 2012·Application pending·0 cites
- 1871US2012149583A1Method for determining copy number variationsRAVA RICHARD P·Filed 2012·Application pending·0 cites
- 1969US2012100548A1Method for determining copy number variationsRAVA RICHARD P·Filed 2011·Application pending·0 cites
- 2068US11875899B2Analyzing copy number variation in the detection of cancerVERINATA HEALTH INC·Filed 2019·Granted Jan 16, 2024·0 cites·17 claims
- 2168US11332774B2Method for determining copy number variationsVERINATA HEALTH INC·Filed 2017·Granted May 17, 2022·0 cites·20 claims
- 2268US2012094849A1Method for determining copy number variationsRAVA RICHARD P·Filed 2011·Application pending·0 cites
- 2360US12205674B2System and method for determining genetic relationships between a sperm provider, oocyte provider, and the respective conceptusCOOPERSURGICAL INC·Filed 2020·Granted Jan 21, 2025·0 cites·5 claims
- 2460US12176069B2Systems and methods for determining pattern of inheritance in embryosCOOPERSURGICAL INC·Filed 2020·Granted Dec 24, 2024·0 cites·14 claims
- 2551US2012270739A1Method for sample analysis of aneuploidies in maternal samplesRAVA RICHARD P·Filed 2012·Application pending·0 cites
- 2651US2012237928A1Method for determining copy number variationsRAVA RICHARD P·Filed 2012·Application pending·0 cites
- 2750US2020399701A1Systems and methods for using density of single nucleotide variations for the verification of copy number variations in human embryosCOOPERSURGICAL INC·Filed 2020·Application pending·0 cites
- 2850US2020402610A1Systems and methods for determining genome ploidyCOOPERSURGICAL INC·Filed 2020·Application pending·0 cites
- 2946US11127485B2Techniques for fine grained correction of count bias in massively parallel DNA sequencingECHELON DIAGNOSTICS INC·Filed 2017·Granted Sep 21, 2021·0 cites·15 claims
- 3046US2009130660A1Single Nucelotide Polymorphism (SNP)FAHAM MALEK·Filed 2005·Application pending·0 cites
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Identity basis: PatentsView inventor disambiguation (2025Q4-odp release). How scoring works →