Issued Patents All Time
Showing 1–25 of 81 patents
| Patent # | Title | Co-Inventors | Date |
|---|---|---|---|
| 12367947 | Normalizing chromosomes for the determination and verification of common and rare chromosomal aneuploidies | — | 2025-07-22 |
| 12139760 | Methods for determining fraction of fetal nucleic acids in maternal samples | Yue-Jen Chuu, Manjula Chinnappa, David A. Comstock, Gabrielle Heilek, Michael W. Hunkapiller | 2024-11-12 |
| 11952623 | Simultaneous determination of aneuploidy and fetal fraction | Stephen R. Quake, Manjula Chinnappa, David A. Comstock, Gabrielle Heilek | 2024-04-09 |
| 11884975 | Sequencing methods and compositions for prenatal diagnoses | Manjula Chinnappa, David A. Comstock, Gabrielle Heilek, Brian K. Rhees | 2024-01-30 |
| 11875899 | Analyzing copy number variation in the detection of cancer | Brian K. Rhees | 2024-01-16 |
| 11697846 | Detecting and classifying copy number variation | Brian K. Rhees | 2023-07-11 |
| 11629378 | Non-invasive prenatal diagnosis of fetal genetic condition using cellular DNA and cell free DNA | Anupama Srinivasan, Darya CHUDOVA | 2023-04-18 |
| 11624064 | Enrichment of mutated cell free nucleic acids for cancer detection | Gordon M. Cann, Alex Aravanis, Arash Jamshidi, Rick Klausner | 2023-04-11 |
| 11430541 | Using cell-free DNA fragment size to determine copy number variations | Sven Duenwald, David A. Comstock, Catalin Barbacioru, Darya CHUDOVA, Keith W. Jones +2 more | 2022-08-30 |
| 11332774 | Method for determining copy number variations | David A. Comstock, Brian K. Rhees | 2022-05-17 |
| 11286520 | Method for determining copy number variations | Brian K. Rhees | 2022-03-29 |
| 11130995 | Simultaneous determination of aneuploidy and fetal fraction | Stephen R. Quake, Manjula Chinnappa, David A. Comstock, Gabrielle Heilek | 2021-09-28 |
| 11072814 | Using cell-free DNA fragment size to determine copy number variations | Darya CHUDOVA, Catalin Barbacioru, Sven Duenwald, David A. Comstock | 2021-07-27 |
| 10941442 | Sequencing methods and compositions for prenatal diagnoses | Manjula Chinnappa, David A. Comstock, Gabrielle Heilek, Brian K. Rhees | 2021-03-09 |
| 10837055 | Non-invasive prenatal diagnosis of fetal genetic condition using cellular DNA and cell free DNA | Anupama Srinivasan, Darya CHUDOVA | 2020-11-17 |
| 10741269 | Method for improving the sensitivity of detection in determining copy number variations | Darya CHUDOVA, Diana Abdueva | 2020-08-11 |
| 10718020 | Methods of fetal abnormality detection | Yue-Jen Chuu | 2020-07-21 |
| 10662474 | Identification of polymorphic sequences in mixtures of genomic DNA by whole genome sequencing | — | 2020-05-26 |
| 10658070 | Resolving genome fractions using polymorphism counts | Brian K. Rhees, John P. Burke | 2020-05-19 |
| 10612096 | Methods for determining fraction of fetal nucleic acids in maternal samples | Yue-Jen Chuu, Manjula Chinnappa, David A. Comstock, Gabrielle Heilek, Michael W. Hunkapiller | 2020-04-07 |
| 10586610 | Detecting and classifying copy number variation | Anupama Srinivasan | 2020-03-10 |
| 10482993 | Analyzing copy number variation in the detection of cancer | Brian K. Rhees | 2019-11-19 |
| 10415089 | Detecting and classifying copy number variation | Brian K. Rhees | 2019-09-17 |
| 10400267 | Generating cell-free DNA libraries directly from blood | Anupama Srinivasan | 2019-09-03 |
| 10388403 | Analyzing copy number variation in the detection of cancer | Brian K. Rhees | 2019-08-20 |