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公开(公告)号:US20220154290A1
公开(公告)日:2022-05-19
申请号:US17568854
申请日:2022-01-05
Applicant: Natera, Inc.
Inventor: Joshua BABIARZ , Tudor Pompiliu CONSTANTIN , Lane A. EUBANK , George GEMELOS , Matthew Micah HILL , Huseyin Eser KIRKIZLAR , Matthew RABINOWITZ , Onur SAKARYA , Styrmir SIGURJONSSON , Bernhard ZIMMERMANN
IPC: C12Q1/6886 , G06N7/00 , G06N20/00 , G16B15/00 , G16B20/00 , G16B20/10 , G16B20/20 , G16B25/00 , G16B40/00 , G16B40/20 , G16H10/40 , G16H50/20 , G16Z99/00 , C12Q1/6869
Abstract: The invention provides methods, systems, and computer readable medium for detecting ploidy of chromosome segments or entire chromosomes, for detecting single nucleotide variants and for detecting both ploidy of chromosome segments and single nucleotide variants. In some aspects, the invention provides methods, systems, and computer readable medium for detecting cancer or a chromosomal abnormality in a gestating fetus.
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公开(公告)号:US20210198742A1
公开(公告)日:2021-07-01
申请号:US17196659
申请日:2021-03-09
Applicant: Natera, Inc.
Inventor: Joshua BABIARZ , Tudor Pompiliu CONSTANTIN , Lane A. EUBANK , George GEMELOS , Matthew Micah HILL , Huseyin Eser KIRKIZLAR , Matthew RABINOWITZ , Onur SAKARYA , Styrmir SIGURJONSSON , Bernhard ZIMMERMANN
IPC: C12Q1/6883 , C12Q1/6811 , C12Q1/6848 , C12Q1/6809 , C12Q1/6851 , C12Q1/6844 , C12Q1/6869 , C12Q1/6855 , C12Q1/6874
Abstract: The invention provides methods for simultaneously amplifying multiple nucleic acid regions of interest in one reaction volume as well as methods for selecting a library of primers for use in such amplification methods. The invention also provides library of primers with desirable characteristics, such as minimal formation of amplified primer dimers or other non-target amplicons.
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公开(公告)号:US20210198733A1
公开(公告)日:2021-07-01
申请号:US17165592
申请日:2021-02-02
Applicant: Natera, Inc.
Inventor: Solomon MOSHKEVICH , Bernhard ZIMMERMANN , Tudor Pompiliu CONSTANTIN , Huseyin Eser KIRKIZLAR , Allison RYAN , Styrmir SIGURJONSSON , Felipe ACOSTA ARCHILA , Ryan SWENERTON
IPC: C12Q1/6869 , C12Q1/6851 , C12Q1/6876
Abstract: The present disclosure provides methods for determining the status of an allograft within a transplant recipient from genotypic data measured from a mixed sample of DNA comprising DNA from both the transplant recipient and from the donor. The mixed sample of DNA may be preferentially enriched at a plurality of polymorphic loci in a way that minimizes the allelic bias, for example using massively multiplexed targeted PCR.
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公开(公告)号:US20200140950A1
公开(公告)日:2020-05-07
申请号:US16743724
申请日:2020-01-15
Applicant: Natera, Inc.
Inventor: Joshua BABIARZ , Tudor Pompiliu CONSTANTIN , Lane A. EUBANK , George GEMELOS , Matthew Micah HILL , Huseyin Eser KIRKIZLAR , Matthew RABINOWITZ , Onur SAKARYA , Styrmir SIGURJONSSON , Bernhard ZIMMERMANN
IPC: C12Q1/6883 , C12Q1/6811 , C12Q1/6848 , C12Q1/6809 , C12Q1/6851 , C12Q1/6855 , C12Q1/6874
Abstract: The invention provides methods for simultaneously amplifying multiple nucleic acid regions of interest in one reaction volume as well as methods for selecting a library of primers for use in such amplification methods. The invention also provides library of primers with desirable characteristics, such as minimal formation of amplified primer dimers or other non-target amplicons.
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公开(公告)号:US20250003000A1
公开(公告)日:2025-01-02
申请号:US18680693
申请日:2024-05-31
Applicant: Natera, Inc.
Inventor: Solomon MOSHKEVICH , Bernhard ZIMMERMANN , Tudor Pompiliu CONSTANTIN , Huseyin Eser KIRKIZLAR , Allison RYAN , Styrmir SIGURJONSSON , Felipe ACOSTA ARCHILA , Ryan SWENERTON
IPC: C12Q1/6883
Abstract: The present disclosure provides methods for determining the status of an allograft within a transplant recipient from genotypic data measured from a mixed sample of DNA comprising DNA from both the transplant recipient and from the donor. The mixed sample of DNA may be preferentially enriched at a plurality of polymorphic loci in a way that minimizes the allelic bias, for example using massively multiplexed targeted PCR.
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公开(公告)号:US20230042405A1
公开(公告)日:2023-02-09
申请号:US17959543
申请日:2022-10-04
Applicant: Natera, Inc.
Inventor: Joshua BABIARZ , Tudor Pompiliu CONSTANTIN , Lane A. EUBANK , George GEMELOS , Matthew Micah HILL , Huseyin Eser KIRKIZLAR , Matthew RABINOWITZ , Onur SAKARYA , Styrmir SIGURJONSSON , Bernhard ZIMMERMANN
IPC: C12Q1/6886 , G06N20/00 , G16B15/00 , G16B25/00 , G16B40/00 , C12Q1/6869 , G16B40/20 , G16B20/10 , G16B20/00 , G16B20/20 , G16Z99/00 , G16H50/20 , G06N7/00 , G16H10/40
Abstract: The invention provides methods, systems, and computer readable medium for detecting ploidy of chromosome segments or entire chromosomes, for detecting single nucleotide variants and for detecting both ploidy of chromosome segments and single nucleotide variants. In some aspects, the invention provides methods, systems, and computer readable medium for detecting cancer or a chromosomal abnormality in a gestating fetus.
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公开(公告)号:US20220403461A1
公开(公告)日:2022-12-22
申请号:US17845169
申请日:2022-06-21
Applicant: Natera, Inc.
Inventor: Huseyin Eser KIRKIZLAR , Raheleh SALARI , Styrmir SIGURJONSSON , Bernhard ZIMMERMANN , Allison RYAN , Naresh VANKAYALAPATI
IPC: C12Q1/6858 , G16B20/00 , C12Q1/6869 , G16B20/10 , G16H10/40 , C12Q1/6886
Abstract: The invention provides improved methods, compositions, and kits for detecting ploidy of chromosome regions, e.g. for detecting cancer or a chromosomal abnormality in a gestating fetus. The methods can utilize a set of more than 200 SNPs that are found within haploblocks and can include analyzing a series of target chromosomal regions related to cancer or a chromosomal abnormality in a gestating fetus. Finally the method may use knowledge about chromosome crossover locations or a best fit algorithm for the analysis. The compositions may comprise more than 200 primers located within haplotype blocks known to show CNV.
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公开(公告)号:US20220033909A1
公开(公告)日:2022-02-03
申请号:US17505588
申请日:2021-10-19
Applicant: Natera, Inc.
Inventor: Joshua BABIARZ , Tudor Pompiliu CONSTANTIN , Lane A. EUBANK , George GEMELOS , Matthew Micah HILL , Huseyin Eser KIRKIZLAR , Matthew RABINOWITZ , Onur SAKARYA , Styrmir SIGURJONSSON , Bernhard ZIMMERMANN
IPC: C12Q1/6883 , C12Q1/6811 , C12Q1/6848 , C12Q1/6809 , C12Q1/6851 , C12Q1/6844 , C12Q1/6869 , C12Q1/6855 , C12Q1/6874
Abstract: The invention provides methods for simultaneously amplifying multiple nucleic acid regions of interest in one reaction volume as well as methods for selecting a library of primers for use in such amplification methods. The invention also provides library of primers with desirable characteristics, such as minimal formation of amplified primer dimers or other non-target amplicons.
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公开(公告)号:US20210025005A1
公开(公告)日:2021-01-28
申请号:US17061877
申请日:2020-10-02
Applicant: Natera, Inc.
Inventor: Joshua BABIARZ , Tudor Pompiliu CONSTANTIN , Lane A. EUBANK , George GEMELOS , Matthew Micah HILL , Huseyin Eser KIRKIZLAR , Matthew RABINOWITZ , Onur SAKARYA , Styrmir SIGURJONSSON , Bernhard ZIMMERMANN
IPC: C12Q1/6883 , C12Q1/6811 , C12Q1/6848 , C12Q1/6809 , C12Q1/6851 , C12Q1/6855 , C12Q1/6874
Abstract: The invention provides methods for simultaneously amplifying multiple nucleic acid regions of interest in one reaction volume as well as methods for selecting a library of primers for use in such amplification methods. The invention also provides library of primers with desirable characteristics, such as minimal formation of amplified primer dimers or other non-target amplicons.
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公开(公告)号:US20190194759A1
公开(公告)日:2019-06-27
申请号:US16288416
申请日:2019-02-28
Applicant: Natera, Inc.
Inventor: Joshua BABIARZ , Tudor Pompiliu CONSTANTIN , Lane A. EUBANK , George GEMELOS , Matthew Micah HILL , Huseyin Eser KIRKIZLAR , Matthew RABINOWITZ , Onur SAKARYA , Styrmir SIGURJONSSON , Bernhard ZIMMERMANN
IPC: C12Q1/6886 , G16B40/00 , G16B25/00 , G16B15/00 , G06N20/00 , G06N7/00 , G16H50/20 , G16H10/40 , C12Q1/6869
CPC classification number: C12Q1/6886 , C12Q1/6869 , C12Q2539/10 , C12Q2600/156 , C12Q2600/158 , C12Q2600/16 , C12Q2600/172 , G06F19/00 , G06N7/005 , G06N20/00 , G16B15/00 , G16B25/00 , G16B40/00 , G16H10/40 , G16H50/20
Abstract: The invention provides methods, systems, and computer readable medium for detecting ploidy of chromosome segments or entire chromosomes, for detecting single nucleotide variants and for detecting both ploidy of chromosome segments and single nucleotide variants. In some aspects, the invention provides methods, systems, and computer readable medium for detecting cancer or a chromosomal abnormality in a gestating fetus.
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