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公开(公告)号:US20240102086A1
公开(公告)日:2024-03-28
申请号:US18370566
申请日:2023-09-20
Applicant: Bio-Rad Laboratories, Inc.
Inventor: Séverine MARGERIDON , Monica HERRERA , Richard DANNEBAUM , Nyaradzo DZVOVA , Raymond-John ABAYAN , Darren R. LINK
IPC: C12Q1/6853
CPC classification number: C12Q1/6853
Abstract: Methods and compositions comprising primers and probes to detect nucleic acids are provided. The probes comprise a ribonucleotide that can be cleaved by an RNase H2 enzyme when the probe is annealed to a reverse complement of a universal sequence that is introduced to a target nucleic acid, for example via amplification.
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公开(公告)号:US20220119896A1
公开(公告)日:2022-04-21
申请号:US17507472
申请日:2021-10-21
Applicant: Bio-Rad Laboratories, Inc.
Inventor: Monica HERRERA , Josh SHINOFF
IPC: C12Q1/70 , C12Q1/689 , C12Q1/6895
Abstract: Methods of concentrating RNA from wastewater and quantifying the RNA by digital amplification are provided.
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公开(公告)号:US20220259680A1
公开(公告)日:2022-08-18
申请号:US17670811
申请日:2022-02-14
Applicant: Bio-Rad Laboratories, Inc. , Biodesix, Inc.
Inventor: Dianna MAAR , Monica HERRERA , George KARLIN-NEUMANN , Josh SHINOFF , Audrey AUDETAT , Scott HUTTON , Hestia MELLERT , Leisa JACKSON , Gary PESTANO
IPC: C12Q1/6888
Abstract: Methods and compositions for characterizing a biological sample (e.g., comprising an infectious agent) from a subject are provided. Methods can include detecting linkage of nucleic acids that are linked in a viable cell or organism but that become degraded and thus unlinked in inviable cells or organisms and then characterizing the subject based on the quantity of linked and unlinked sequences.
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公开(公告)号:US20240084374A1
公开(公告)日:2024-03-14
申请号:US18465321
申请日:2023-09-12
Applicant: Bio-Rad Laboratories, Inc.
Inventor: Chenyu LI , Olga MIKHAYLICHENKO , Nathan HENDEL , Anthony HENRIQUEZ , Richard DANNEBAUM , Monica HERRERA , Eric HALL , Séverine MARGERIDON , Thea RIEL
IPC: C12Q1/686
CPC classification number: C12Q1/686 , C12Q2600/154
Abstract: The digital amplification methods and kits provide the ability to estimate the fetal fraction of cell-free DNA (cfDNA) in a maternal sample, e.g., plasma or serum, by analysis of target sites that are differentially methylated in fetal and maternal cfDNA.
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