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公开(公告)号:US09745626B2
公开(公告)日:2017-08-29
申请号:US15222875
申请日:2016-07-28
Applicant: Personalis, Inc.
Inventor: Gabor T. Bartha , Gemma Chandratillake , Richard Chen , Sarah Garcia , Hugo Yu Kor Lam , Shujun Luo , Mark R. Pratt , John West
CPC classification number: C12Q1/6874 , C12Q1/6806 , C12Q1/6869 , C40B50/02 , G06F19/10 , G06F19/18 , G06F19/22
Abstract: This disclosure provides systems and methods for sample processing and data analysis. Sample processing may include nucleic acid sample processing and subsequent sequencing. Some or all of a nucleic acid sample may be sequenced to provide sequence information, which may be stored or otherwise maintained in an electronic storage location. The sequence information may be analyzed with the aid of a computer processor, and the analyzed sequence information may be stored in an electronic storage location that may include a pool or collection of sequence information and analyzed sequence information generated from the nucleic acid sample. Methods and systems of the present disclosure can be used, for example, for the analysis of a nucleic acid sample, for producing one or more libraries, and for producing biomedical reports. Methods and systems of the disclosure can aid in the diagnosis, monitoring, treatment, and prevention of one or more diseases and conditions.
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公开(公告)号:US09128861B2
公开(公告)日:2015-09-08
申请号:US14141990
申请日:2013-12-27
Applicant: Personalis, Inc.
Inventor: Gabor T. Bartha , Gemma Chandratillake , Richard Chen , Sarah Garcia , Hugo Yu Kor Lam , Shujun Luo , Mark R. Pratt , John West
CPC classification number: C12Q1/6874 , C12Q1/6806 , C12Q1/6869 , C40B50/02 , G06F19/10 , G06F19/18 , G06F19/22
Abstract: This disclosure provides systems and methods for sample processing and data analysis. Sample processing may include nucleic acid sample processing and subsequent sequencing. Some or all of a nucleic acid sample may be sequenced to provide sequence information, which may be stored or otherwise maintained in an electronic storage location. The sequence information may be analyzed with the aid of a computer processor, and the analyzed sequence information may be stored in an electronic storage location that may include a pool or collection of sequence information and analyzed sequence information generated from the nucleic acid sample. Methods and systems of the present disclosure can be used, for example, for the analysis of a nucleic acid sample, for producing one or more libraries, and for producing biomedical reports. Methods and systems of the disclosure can aid in the diagnosis, monitoring, treatment, and prevention of one or more diseases and conditions.
Abstract translation: 本公开提供了用于样本处理和数据分析的系统和方法。 样品处理可包括核酸样品处理和随后的测序。 可以对核酸样品中的一些或全部进行测序以提供可存储或以其他方式保存在电子存储位置中的序列信息。 可以借助于计算机处理器来分析序列信息,并且所分析的序列信息可以存储在电子存储位置中,该电子存储位置可以包括从核酸样品产生的序列信息和分析的序列信息的集合或集合。 本公开的方法和系统可用于例如核酸样品的分析,用于产生一个或多个文库以及用于生产生物医学报告。 本公开的方法和系统可以帮助诊断,监测,治疗和预防一种或多种疾病和病症。
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公开(公告)号:US12084717B2
公开(公告)日:2024-09-10
申请号:US18312710
申请日:2023-05-05
Applicant: Personalis, Inc.
Inventor: Gabor T. Bartha , Gemma Chandratillake , Richard Chen , Sarah Garcia , Hugo Yu Kor Lam , Shujun Luo , Mark R. Pratt , John West
IPC: C12Q1/6874 , C12Q1/6806 , C12Q1/6869 , G16B20/00 , G16B20/10 , G16B20/20 , G16B30/00 , G16B35/00 , G16B35/10 , G16B99/00 , G16C20/60
CPC classification number: C12Q1/6874 , C12Q1/6806 , G16B20/00 , G16B20/10 , G16B20/20 , G16B30/00 , G16B35/10 , G16B99/00 , C12Q1/6869 , G16B35/00 , G16C20/60
Abstract: This disclosure provides systems and methods for sample processing and data analysis. Sample processing may include nucleic acid sample processing and subsequent sequencing. Some or all of a nucleic acid sample may be sequenced to provide sequence information, which may be stored or otherwise maintained in an electronic storage location. The sequence information may be analyzed with the aid of a computer processor, and the analyzed sequence information may be stored in an electronic storage location that may include a pool or collection of sequence information and analyzed sequence information generated from the nucleic acid sample. Methods and systems of the present disclosure can be used, for example, for the analysis of a nucleic acid sample, for producing one or more libraries, and for producing biomedical reports. Methods and systems of the disclosure can aid in the diagnosis, monitoring, treatment, and prevention of one or more diseases and conditions.
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公开(公告)号:US11976326B2
公开(公告)日:2024-05-07
申请号:US18178764
申请日:2023-03-06
Applicant: Personalis, Inc.
Inventor: Gabor T. Bartha , Gemma Chandratillake , Richard Chen , Sarah Garcia , Hugo Yu Kor Lam , Shujun Luo , Mark R. Pratt , John West
IPC: C12Q1/6874 , C12Q1/6806 , C12Q1/6869 , G16B20/00 , G16B20/10 , G16B20/20 , G16B30/00 , G16B35/00 , G16B35/10 , G16B99/00 , G16C20/60
CPC classification number: C12Q1/6874 , C12Q1/6806 , G16B20/00 , G16B20/10 , G16B20/20 , G16B30/00 , G16B35/10 , G16B99/00 , C12Q1/6869 , G16B35/00 , G16C20/60
Abstract: This disclosure provides systems and methods for sample processing and data analysis. Sample processing may include nucleic acid sample processing and subsequent sequencing. Some or all of a nucleic acid sample may be sequenced to provide sequence information, which may be stored or otherwise maintained in an electronic storage location. The sequence information may be analyzed with the aid of a computer processor, and the analyzed sequence information may be stored in an electronic storage location that may include a pool or collection of sequence information and analyzed sequence information generated from the nucleic acid sample. Methods and systems of the present disclosure can be used, for example, for the analysis of a nucleic acid sample, for producing one or more libraries, and for producing biomedical reports. Methods and systems of the disclosure can aid in the diagnosis, monitoring, treatment, and prevention of one or more diseases and conditions.
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公开(公告)号:US11643685B2
公开(公告)日:2023-05-09
申请号:US17747436
申请日:2022-05-18
Applicant: Personalis, Inc.
Inventor: John West , Christian Haudenschild , Richard Chen
IPC: C12Q1/6874 , G16B99/00 , G16B20/00 , G16B30/00 , C12Q1/6806 , G16C20/60 , G16B35/00 , C12Q1/6869
CPC classification number: C12Q1/6874 , C12Q1/6806 , G16B20/00 , G16B30/00 , G16B99/00 , C12Q1/6869 , G16B35/00 , G16C20/60
Abstract: This disclosure provides systems and methods for sample processing and data analysis. Sample processing may include nucleic acid sample processing and subsequent sequencing. Some or all of a nucleic acid sample may be sequenced to provide sequence information, which may be stored or otherwise maintained in an electronic storage location. The sequence information may be analyzed with the aid of a computer processor, and the analyzed sequence information may be stored in an electronic storage location that may include a pool or collection of sequence information and analyzed sequence information generated from the nucleic acid sample. Methods and systems of the present disclosure can be used, for example, for the analysis of a nucleic acid sample, for producing one or more libraries, and for producing biomedical reports. Methods and systems of the disclosure can aid in the diagnosis, monitoring, treatment, and prevention of one or more diseases and conditions.
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公开(公告)号:US20230089500A1
公开(公告)日:2023-03-23
申请号:US18058376
申请日:2022-11-23
Applicant: Personalis, Inc.
Inventor: Gabor T. Bartha , Gemma Chandratillake , Richard Chen , Sarah Garcia , Hugo Yu Kor Lam , Shujun Luo , Mark R. Pratt , John West
IPC: C12Q1/6874 , G16B20/00 , G16B30/00 , G16B99/00 , G16B20/10 , G16B20/20 , G16B35/10 , C12Q1/6806
Abstract: This disclosure provides systems and methods for sample processing and data analysis. Sample processing may include nucleic acid sample processing and subsequent sequencing. Some or all of a nucleic acid sample may be sequenced to provide sequence information, which may be stored or otherwise maintained in an electronic storage location. The sequence information may be analyzed with the aid of a computer processor, and the analyzed sequence information may be stored in an electronic storage location that may include a pool or collection of sequence information and analyzed sequence information generated from the nucleic acid sample. Methods and systems of the present disclosure can be used, for example, for the analysis of a nucleic acid sample, for producing one or more libraries, and for producing biomedical reports. Methods and systems of the disclosure can aid in the diagnosis, monitoring, treatment, and prevention of one or more diseases and conditions.
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公开(公告)号:US20220392577A1
公开(公告)日:2022-12-08
申请号:US17817581
申请日:2022-08-04
Applicant: Personalis, Inc.
Inventor: Jason Harris , Mark R. Pratt , John West , Richard Chen , Ming Li
Abstract: A computer-implemented method for processing and/or analyzing nucleic acid sequencing data comprises receiving a first data input and a second data input. The first data input comprises untargeted sequencing data generated from a first nucleic acid sample obtained from a subject. The second data input comprises target-specific sequencing data generated from a second nucleic acid sample obtained from the subject. Next, with the aid of a computer processor, the first data input and the second data input are combined to produce a combined data set. Next, an output derived from the combined data set is generated. The output is indicative of the presence or absence of one or more polymorphisms of the first nucleic acid sample and/or the second nucleic acid sample.
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公开(公告)号:US20220277810A1
公开(公告)日:2022-09-01
申请号:US17746669
申请日:2022-05-17
Applicant: Personalis, Inc.
Inventor: Jason Harris , Mark R. Pratt , John West , Richard Chen , Ming Li
Abstract: A computer-implemented method for processing and/or analyzing nucleic acid sequencing data comprises receiving a first data input and a second data input. The first data input comprises untargeted sequencing data generated from a first nucleic acid sample obtained from a subject. The second data input comprises target-specific sequencing data generated from a second nucleic acid sample obtained from the subject. Next, with the aid of a computer processor, the first data input and the second data input are combined to produce a combined data set. Next, an output derived from the combined data set is generated. The output is indicative of the presence or absence of one or more polymorphisms of the first nucleic acid sample and/or the second nucleic acid sample.
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公开(公告)号:US11299783B2
公开(公告)日:2022-04-12
申请号:US17235776
申请日:2021-04-20
Applicant: Personalis, Inc.
Inventor: John West , Christian Haudenschild , Richard Chen
IPC: C12Q1/6874 , G16B20/00 , C12Q1/6806 , C12Q1/6869 , G16B35/00 , G16C20/60 , G16B30/00 , G16B99/00
Abstract: This disclosure provides systems and methods for sample processing and data analysis. Sample processing may include nucleic acid sample processing and subsequent sequencing. Some or all of a nucleic acid sample may be sequenced to provide sequence information, which may be stored or otherwise maintained in an electronic storage location. The sequence information may be analyzed with the aid of a computer processor, and the analyzed sequence information may be stored in an electronic storage location that may include a pool or collection of sequence information and analyzed sequence information generated from the nucleic acid sample. Methods and systems of the present disclosure can be used, for example, for the analysis of a nucleic acid sample, for producing one or more libraries, and for producing biomedical reports. Methods and systems of the disclosure can aid in the diagnosis, monitoring, treatment, and prevention of one or more diseases and conditions.
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公开(公告)号:US20220081716A1
公开(公告)日:2022-03-17
申请号:US17355688
申请日:2021-06-23
Applicant: Personalis, Inc.
Inventor: John West , Christian Haudenschild , Richard Chen
IPC: C12Q1/6883 , G16B30/00 , C12Q1/68 , G16B20/00 , G16B99/00 , G06N3/12 , G16B20/10 , G16B20/40 , G16B20/20 , C12Q1/6853 , C12Q1/6869
Abstract: The present disclosure provides methods and systems for personalized genetic testing of a subject. In some embodiments, a sequencing assay is performed on a biological sample from the subject, which then leads to genetic information related to the subject. Next, nucleic acid molecules are array-synthesized or selected based on the genetic information derived from data of the sequencing assay. At least some of the nucleic acid molecules may then be used in an assay which may provide additional information on one or more biological samples from the subject or a biological relative of the subject.
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