Assignee
VERINATA HEALTH INC
US·39 granted patents·19 pending applications·218 citations·filing 2012–2025
Top patents by PatentIndex Score
58 records- 0196US11130995B2Simultaneous determination of aneuploidy and fetal fractionVERINATA HEALTH INC·Filed 2017·Granted Sep 28, 2021·54 cites·17 claims
- 0296US9347100B2Rare cell analysis using sample splitting and DNA tagsVERINATA HEALTH INC·Filed 2013·Granted May 24, 2016·12 cites·27 claims
- 0395US10415089B2Detecting and classifying copy number variationVERINATA HEALTH INC·Filed 2015·Granted Sep 17, 2019·14 cites·26 claims
- 0495US9017942B2Rare cell analysis using sample splitting and DNA tagsVERINATA HEALTH INC·Filed 2013·Granted Apr 28, 2015·14 cites·24 claims
- 0595US2026098295A1Sequencing methods and compositions for prenatal diagnosesVERINATA HEALTH INC·Filed 2025·Application pending·0 cites
- 0694US10095831B2Using cell-free DNA fragment size to determine copy number variationsVERINATA HEALTH INC·Filed 2016·Granted Oct 9, 2018·28 cites·33 claims
- 0792US11884975B2Sequencing methods and compositions for prenatal diagnosesVERINATA HEALTH INC·Filed 2021·Granted Jan 30, 2024·2 cites·10 claims
- 0892US10482993B2Analyzing copy number variation in the detection of cancerVERINATA HEALTH INC·Filed 2016·Granted Nov 19, 2019·11 cites·29 claims
- 0992US9493831B2Methods of fetal abnormality detectionVERINATA HEALTH INC·Filed 2015·Granted Nov 15, 2016·6 cites·24 claims
- 1091US10941442B2Sequencing methods and compositions for prenatal diagnosesVERINATA HEALTH INC·Filed 2017·Granted Mar 9, 2021·5 cites·6 claims
- 1191US10318704B2Detecting fetal sub-chromosomal aneuploidiesVERINATA HEALTH INC·Filed 2015·Granted Jun 11, 2019·6 cites·27 claims
- 1291US9273355B2Rare cell analysis using sample splitting and DNA tagsVERINATA HEALTH INC·Filed 2013·Granted Mar 1, 2016·7 cites·12 claims
- 1390US10741269B2Method for improving the sensitivity of detection in determining copy number variationsVERINATA HEALTH INC·Filed 2014·Granted Aug 11, 2020·24 cites·39 claims
- 1490US10612096B2Methods for determining fraction of fetal nucleic acids in maternal samplesVERINATA HEALTH INC·Filed 2016·Granted Apr 7, 2020·5 cites·18 claims
- 1590US10586610B2Detecting and classifying copy number variationVERINATA HEALTH INC·Filed 2016·Granted Mar 10, 2020·4 cites·22 claims
- 1689US2026038632A1Resolving genome fractions using polymorphism countsVERINATA HEALTH INC·Filed 2025·Application pending·0 cites
- 1788US11072814B2Using cell-free DNA fragment size to determine copy number variationsVERINATA HEALTH INC·Filed 2015·Granted Jul 27, 2021·4 cites·36 claims
- 1888US10041119B2Methods for the diagnosis of fetal abnormalitiesVERINATA HEALTH INC·Filed 2015·Granted Aug 7, 2018·2 cites·12 claims
- 1988US10017807B2Generating cell-free DNA libraries directly from bloodVERINATA HEALTH INC·Filed 2014·Granted Jul 10, 2018·4 cites·35 claims
- 2087US2025109439A1Methods for determining fraction of fetal nucleic acids in maternal samplesVERINATA HEALTH INC·Filed 2024·Application pending·0 cites
- 2186US12522869B2Sequencing methods and compositions for prenatal diagnosesVERINATA HEALTH INC·Filed 2023·Granted Jan 13, 2026·0 cites·15 claims
- 2286US9845552B2Set membership testers for aligning nucleic acid samplesVERINATA HEALTH INC·Filed 2012·Granted Dec 19, 2017·11 cites·21 claims
- 2386US2024141424A1Fetal aneuploidy detection by sequencingVERINATA HEALTH INC·Filed 2023·Application pending·0 cites
- 2482US9115401B2Partition defined detection methodsVERINATA HEALTH INC·Filed 2014·Granted Aug 25, 2015·1 cites·47 claims
- 2581US10718020B2Methods of fetal abnormality detectionVERINATA HEALTH INC·Filed 2016·Granted Jul 21, 2020·1 cites·23 claims
- 2681US10658070B2Resolving genome fractions using polymorphism countsVERINATA HEALTH INC·Filed 2016·Granted May 19, 2020·1 cites·21 claims
- 2779US12553084B2Method for determining copy number variationsVERINATA HEALTH INC·Filed 2021·Granted Feb 17, 2026·0 cites·17 claims
- 2879US11952623B2Simultaneous determination of aneuploidy and fetal fractionVERINATA HEALTH INC·Filed 2021·Granted Apr 9, 2024·0 cites·19 claims
- 2979US11430541B2Using cell-free DNA fragment size to determine copy number variationsVERINATA HEALTH INC·Filed 2018·Granted Aug 30, 2022·2 cites·23 claims
- 3078US2023340590A1Method for verifying bioassay samplesVERINATA HEALTH INC·Filed 2023·Application pending·0 cites
- 3178US2022228197A1Method for determining copy number variationsVERINATA HEALTH INC·Filed 2022·Application pending·0 cites
- 3277US2023044849A1Using cell-free dna fragment size to determine copy number variationsVERINATA HEALTH INC·Filed 2022·Application pending·0 cites
- 3375US12367947B2Normalizing chromosomes for the determination and verification of common and rare chromosomal aneuploidiesVERINATA HEALTH INC·Filed 2020·Granted Jul 22, 2025·0 cites·17 claims
- 3475US11674176B2Fetal aneuploidy detection by sequencingVERINATA HEALTH INC·Filed 2020·Granted Jun 13, 2023·0 cites·11 claims
- 3575US11378498B2Diagnosis of fetal abnormalities using polymorphisms including short tandem repeatsVERINATA HEALTH INC·Filed 2020·Granted Jul 5, 2022·0 cites·20 claims
- 3673US11697846B2Detecting and classifying copy number variationVERINATA HEALTH INC·Filed 2019·Granted Jul 11, 2023·0 cites·19 claims
- 3773US10591391B2Diagnosis of fetal abnormalities using polymorphisms including short tandem repeatsVERINATA HEALTH INC·Filed 2013·Granted Mar 17, 2020·0 cites·17 claims
- 3873US2020251180A1Resolving genome fractions using polymorphism countsVERINATA HEALTH INC·Filed 2020·Application pending·0 cites
- 3973US2013324420A1Normalizing chromosomes for the determination and verification of common and rare chromosomal aneuploidiesVERINATA HEALTH INC·Filed 2013·Application pending·0 cites
- 4073US2024203601A1Analyzing copy number variation in the detection of cancerVERINATA HEALTH INC·Filed 2023·Application pending·0 cites
- 4172US10704090B2Fetal aneuploidy detection by sequencingVERINATA HEALTH INC·Filed 2013·Granted Jul 7, 2020·0 cites·11 claims
- 4272US2020219588A1Detecting and classifying copy number variationVERINATA HEALTH INC·Filed 2020·Application pending·0 cites
- 4372US2021054458A1Methods of fetal abnormality detectionVERINATA HEALTH INC·Filed 2020·Application pending·0 cites
- 4471US12139760B2Methods for determining fraction of fetal nucleic acids in maternal samplesVERINATA HEALTH INC·Filed 2020·Granted Nov 12, 2024·0 cites·16 claims
- 4571US11286520B2Method for determining copy number variationsVERINATA HEALTH INC·Filed 2017·Granted Mar 29, 2022·0 cites·21 claims
- 4670US2021371907A1Using cell-free dna fragment size to determine copy number variationsVERINATA HEALTH INC·Filed 2021·Application pending·0 cites
- 4769US10400267B2Generating cell-free DNA libraries directly from bloodVERINATA HEALTH INC·Filed 2018·Granted Sep 3, 2019·0 cites·19 claims
- 4869US2014199691A1Methods of fetal abnormality detectionVERINATA HEALTH INC·Filed 2013·Application pending·0 cites
- 4969US2019338345A1Generating cell-free dna libraries directly from bloodVERINATA HEALTH INC·Filed 2019·Application pending·0 cites
- 5068US11875899B2Analyzing copy number variation in the detection of cancerVERINATA HEALTH INC·Filed 2019·Granted Jan 16, 2024·0 cites·17 claims
Showing the top 50 of 58 patent records by PatentIndex Score.
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