METHODS FOR PREPARING NUCLEIC ACID MOLECULES
    33.
    发明申请

    公开(公告)号:US20190127731A1

    公开(公告)日:2019-05-02

    申请号:US16196684

    申请日:2018-11-20

    Abstract: Provided herein are methods for preparing nucleic acid molecules for sequencing. The methods may include generation of individual partitions (e.g., droplets or wells) including a biological particle and a bead comprising a nucleic acid barcode molecule. The preparation of barcoded nucleic acid molecules for sequencing can include subjecting the nucleic acid molecule to DNase treatment followed by attachment of a nucleic acid barcode molecule.

    Methods and compositions for analyzing target binding of molecules

    公开(公告)号:US12298314B2

    公开(公告)日:2025-05-13

    申请号:US17497135

    申请日:2021-10-08

    Abstract: The present disclosure relates in some aspects to methods and compositions for assessing the target binding capacity of a binding molecule, such as an antigen binding molecule, e.g., a monoclonal antibody. In some embodiments, provided herein is a method of analyzing binding of a barcode-labeled antibody to a target antigen expressed by a cell, wherein cells expressing the candidate antigens are partitioned and wherein detection of the barcoded nucleic acid molecule is indicative of the binding between the antibody or antigen-binding fragment thereof and the candidate antigen or epitope of the cell.

    Analysis of nucleic acid sequences
    35.
    发明授权

    公开(公告)号:US12275993B2

    公开(公告)日:2025-04-15

    申请号:US18929514

    申请日:2024-10-28

    Abstract: The present disclosure relates to methods, compositions and systems for droplet processing. For example, methods can include (a) providing a first emulsion comprising a first droplet population, wherein droplets of the first droplet population comprise a lysis reagent, and a second emulsion comprising a second droplet population, wherein a droplet of the second droplet population comprises i) a cell or a nucleus, and ii) a plurality of nucleic acid barcode molecules; (b) subjecting the first emulsion and second emulsion to conditions sufficient to transfer the lysis reagent to the second droplet population via micelles comprising the lysis reagent; and (c) lysing the cell or the nucleus within the droplet of the second droplet population with the lysis reagent.

    Single cell analysis of transposase accessible chromatin

    公开(公告)号:US11773389B2

    公开(公告)日:2023-10-03

    申请号:US17492536

    申请日:2021-10-01

    CPC classification number: C12N15/1065 C12N15/1068 C12N15/1075 C12N15/1096

    Abstract: Methods and systems for sample preparation techniques that allow amplification (e.g., whole genome amplification) and sequencing of chromatin accessible regions of single cells are provided. The methods and systems generally operate by forming or providing partitions (e.g., droplets) including a single biological particle and a single bead comprising a barcoded oligonucleotide. The preparation of barcoded next-generation sequencing libraries prepared from a single cell is facilitated by the transposon-mediated transposition and fragmentation of a target nucleic acid sequence. The methods and systems may be configured to allow the implementation of single-operation or multi-operation chemical and/or biochemical processing within the partitions.

    SYSTEMS AND METHODS FOR TRANSFER OF REAGENTS BETWEEN DROPLETS

    公开(公告)号:US20220025438A1

    公开(公告)日:2022-01-27

    申请号:US17397775

    申请日:2021-08-09

    Abstract: The disclosure provides systems and methods for droplet processing. For example, a method can include providing a first droplet and a second droplet. In some cases, the first droplet may have a first concentration of a reagent and the second droplet may have a second concentration of the reagent. The second droplet may comprise a bead or a biological particle. The method can also include subjecting the first droplet and the second droplet to conditions sufficient to transfer the reagent from the first droplet to the second droplet, thereby decreasing the first concentration in the first droplet and increasing the second concentration in the second droplet.

    Single cell analysis of transposase accessible chromatin

    公开(公告)号:US11155810B2

    公开(公告)日:2021-10-26

    申请号:US16841411

    申请日:2020-04-06

    Abstract: Methods and systems for sample preparation techniques that allow amplification (e.g., whole genome amplification) and sequencing of chromatin accessible regions of single cells are provided. The methods and systems generally operate by forming or providing partitions (e.g., droplets) including a single biological particle and a single bead comprising a barcoded oligonucleotide. The preparation of barcoded next-generation sequencing libraries prepared from a single cell is facilitated by the transposon-mediated transposition and fragmentation of a target nucleic acid sequence. The methods and systems may be configured to allow the implementation of single-operation or multi-operation chemical and/or biochemical processing within the partitions.

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