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公开(公告)号:US12049712B2
公开(公告)日:2024-07-30
申请号:US17229859
申请日:2021-04-13
Applicant: 10X Genomics, Inc.
Inventor: Jason Bell , Francesca Meschi , Geoffrey McDermott , Michael Schnall-Levin , Xinying Zheng
IPC: C40B30/04 , C07K14/74 , C12N15/10 , C12N15/11 , C12N15/85 , C12Q1/6804 , C12Q1/6806 , C12Q1/6818 , C12Q1/6827 , C12Q1/6881 , C40B50/06 , C40B70/00 , G01N33/50 , G01N33/53 , G01N33/532 , G01N33/543 , G01N33/548 , G01N33/569 , G01N33/58
CPC classification number: C40B30/04 , C07K14/70539 , C12N15/1037 , C12N15/1055 , C12N15/1065 , C12N15/1075 , C12N15/11 , C12N15/85 , C12Q1/6804 , C12Q1/6806 , C12Q1/6818 , C12Q1/6827 , C12Q1/6881 , G01N33/5032 , G01N33/505 , G01N33/5304 , G01N33/5306 , G01N33/5308 , G01N33/532 , G01N33/54306 , G01N33/54366 , G01N33/548 , G01N33/56977 , G01N33/58 , C12N2310/20 , C12N2320/10 , C12Q2537/164 , C12Q2563/179 , C12Q2563/185 , C12Q2565/1015 , C40B50/06 , C40B70/00
Abstract: The present disclosure provides compositions, methods, systems, and devices for polynucleotide processing and analyte characterization from a single cell. Such polynucleotide processing may be useful for a variety of applications. The compositions, methods, systems, and devices disclosed herein generally describe barcoded oligonucleotides, which can be bound to a bead, such as a gel bead, useful for characterizing one or more analytes including, for example, protein (e.g., cell surface or intracellular proteins) and chromatin (e.g., accessible chromatin).
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公开(公告)号:US20230383440A1
公开(公告)日:2023-11-30
申请号:US18231460
申请日:2023-08-08
Applicant: 10x Genomics, Inc.
Inventor: Jason Bell , Francesca Meschi , Geoffrey McDermott , Michael Schnall-Levin , Xinying Zheng
IPC: C40B30/04 , C07K14/74 , C12N15/85 , G01N33/532 , G01N33/543 , G01N33/548 , C12N15/10 , C12Q1/6804 , C12Q1/6806 , G01N33/50 , G01N33/53 , G01N33/58 , C12Q1/6818 , C12Q1/6827 , C12Q1/6881 , C12N15/11 , G01N33/569
CPC classification number: C40B30/04 , C07K14/70539 , C12N15/85 , G01N33/532 , G01N33/54306 , G01N33/548 , C12N15/1037 , C12N15/1075 , C12Q1/6804 , C12Q1/6806 , G01N33/505 , G01N33/5308 , G01N33/58 , C12Q1/6818 , C12Q1/6827 , C12Q1/6881 , C12N15/11 , G01N33/5304 , G01N33/5306 , C12N15/1055 , C12N15/1065 , G01N33/5032 , G01N33/54366 , G01N33/56977 , C12Q2537/164 , C12Q2565/1015 , C12Q2563/179 , C12Q2563/185 , C12N2310/20 , C40B70/00
Abstract: The present disclosure provides compositions, methods, systems, and devices for polynucleotide processing and analyte characterization from a single cell. Such polynucleotide processing may be useful for a variety of applications. The compositions, methods, systems, and devices disclosed herein generally describe barcoded oligonucleotides, which can be bound to a bead, such as a gel bead, useful for characterizing one or more analytes.
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公开(公告)号:US20210270818A1
公开(公告)日:2021-09-02
申请号:US17229859
申请日:2021-04-13
Applicant: 10X Genomics, Inc.
Inventor: Jason Bell , Francesca Meschi , Geoffrey McDermott , Michael Schnall-Levin , Xinying Zheng
IPC: G01N33/532 , C07K14/74 , C12N15/85 , G01N33/543 , G01N33/548 , C12N15/10 , C12Q1/6804 , C12Q1/6806 , G01N33/50 , G01N33/53 , G01N33/58 , C12Q1/6818 , C12Q1/6827 , C12Q1/6881 , C12N15/11 , G01N33/569
Abstract: The present disclosure provides compositions, methods, systems, and devices for polynucleotide processing and analyte characterization from a single cell. Such polynucleotide processing may be useful for a variety of applications. The compositions, methods, systems, and devices disclosed herein generally describe barcoded oligonucleotides, which can be bound to a bead, such as a gel bead, useful for characterizing one or more analytes including, for example, protein (e.g., cell surface or intracellular proteins) and chromatin (e.g., accessible chromatin).
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公开(公告)号:US20190367966A1
公开(公告)日:2019-12-05
申请号:US16375102
申请日:2019-04-04
Applicant: 10X Genomics, Inc.
Inventor: Kamila Belhocine , Jason Bell , Zachary Bent , Rajiv Bharadwaj , Christopher Hindson , Mohammad Rahimi Lenji , Bill Kengli Lin , Anthony Makarewicz , Geoffrey McDermott , Elliott Meer , Francesca Meschi , Tarjei Sigurd Mikkelsen , Christopher Joachim O'Keeffe , Katherine Pfeiffer , Andrew D. Price , Paul Ryvkin , Michael Schnall-Levin , Sarah Taylor , Jessica Michele Terry , Tobias Daniel Wheeler , Yifeng Yin , Xinying Zheng , Solongo Batjargal Ziraldo , Eswar Prasad Ramachandran Iyer , Luigi Jhon Alvarado Martinez
IPC: C12Q1/6806 , G01N33/53 , G01N33/58 , C12Q1/6804 , G01N33/50 , C12N15/10
Abstract: The present disclosure provides compositions, methods, systems, and devices for polynucleotide processing and analyte characterization from one or more cells. Such polynucleotide processing may be useful for a variety of applications, including characterization of major histocompatibility complex (MHC) molecules. The compositions, methods, systems, and devices disclosed herein generally describe peptides and barcoded oligonucleotides, which can be bound to a bead, such as a gel bead, useful for characterizing MHC molecules from one or more cells.
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公开(公告)号:US20180340171A1
公开(公告)日:2018-11-29
申请号:US15842713
申请日:2017-12-14
Applicant: 10X Genomics, Inc.
Inventor: Kamila Belhocine , Geoffrey McDermott , Francesca Meschi , Xinying Zheng
IPC: C12N15/10
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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公开(公告)号:US20250115946A1
公开(公告)日:2025-04-10
申请号:US18926858
申请日:2024-10-25
Applicant: 10x Genomics, Inc.
Inventor: Jason Bell , Josephine Lee , Corey Nemec , Francesca Meschi
IPC: C12Q1/6806 , C12N9/12 , C12N15/10
Abstract: Methods and compositions to minimize barcode exchange during the preparation of barcoded next-generation sequencing libraries prepared from a single cell. The methods utilize oligonucleotides containing a 3′-terminated blocking group or sequences that prevent amplification or extension.
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公开(公告)号:US20240401240A1
公开(公告)日:2024-12-05
申请号:US18742590
申请日:2024-06-13
Applicant: 10x Genomics, Inc.
Inventor: Jason Bell , Francesca Meschi , Geoffrey McDermott , Michael Schnall-Levin , Xinying Zheng
IPC: C40B30/04 , C07K14/74 , C12N15/10 , C12N15/11 , C12N15/85 , C12Q1/6804 , C12Q1/6806 , C12Q1/6818 , C12Q1/6827 , C12Q1/6881 , C40B50/06 , C40B70/00 , G01N33/50 , G01N33/53 , G01N33/532 , G01N33/543 , G01N33/548 , G01N33/569 , G01N33/58
Abstract: The present disclosure provides compositions, methods, systems, and devices for polynucleotide processing and analyte characterization from a single cell. Such polynucleotide processing may be useful for a variety of applications. The compositions, methods, systems, and devices disclosed herein generally describe barcoded oligonucleotides, which can be bound to a bead, such as a gel bead, useful for characterizing one or more analytes including, for example, protein (e.g., cell surface or intracellular proteins) and chromatin (e.g., accessible chromatin).
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公开(公告)号:US20240084292A1
公开(公告)日:2024-03-14
申请号:US18355946
申请日:2023-07-20
Applicant: 10x Genomics, Inc.
Inventor: Zahra Kamila Belhocine , Geoffrey McDermott , Francesca Meschi , Xinying Zheng
IPC: C12N15/10
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.
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公开(公告)号:US11198866B2
公开(公告)日:2021-12-14
申请号:US16206168
申请日:2018-11-30
Applicant: 10X Genomics, Inc.
Inventor: Zahra Kamila Belhocine , Geoffrey McDermott , Francesca Meschi , Xinying Zheng
IPC: C12N15/10
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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公开(公告)号:US20210115415A1
公开(公告)日:2021-04-22
申请号:US17114016
申请日:2020-12-07
Applicant: 10X Genomics, Inc.
Inventor: Josephine Lee , Samuel Marrs , Geoffrey McDermott , Francesca Meschi , Luz Montesclaros , Katherine Pfeiffer , Joseph Francis Shuga , Jessica Michele Terry , Solongo B. Ziraldo
IPC: C12N9/12 , C12N15/10 , C12Q1/6806 , C12Q1/6844
Abstract: Disclosed herein, are compositions, methods, and kits comprising engineered reverse transcription enzymes that exhibit several desired properties such as thermal stability, processive reverse transcription, non-templated base addition, and template switching ability. The engineered reverse transcription enzymes described herein demonstrate unexpectedly higher resistance to cell lysate inhibition, greater ability to capture full-length mRNA transcripts, and demonstrate improved results in small reaction volumes as compared to other engineered reverse transcription enzymes.
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