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公开(公告)号:US11790282B1
公开(公告)日:2023-10-17
申请号:US17742337
申请日:2022-05-11
Applicant: Color Health, Inc.
Inventor: Ryan Barrett , Nishant Bhat , Huy Hong , Katsuya Noguchi , Wendy McKennon , Krishna Pant , Taylor Sittler , Othman Laraki , Elad Gil
IPC: G06Q10/00 , H01L21/768 , G16H10/60 , G16B20/20 , G16B25/00 , G06F18/23 , G06F18/20 , G16B20/10 , G16H40/67 , G16B25/10 , G06Q10/063 , G16B50/00 , G16B30/10 , G16B30/00
CPC classification number: G06Q10/00 , G06F18/23 , G06F18/285 , G16B20/20 , G16B25/00 , G16H10/60 , H01L21/76886 , G06F2218/00 , G06Q10/063 , G16B20/10 , G16B25/10 , G16B30/00 , G16B30/10 , G16B50/00 , G16H40/67 , H01L21/768
Abstract: Genetic-variant data is obtained that corresponds to one or more variants associated with a client. Each of the one or more variants corresponds to an instance of one or more bases positioned at one or more first positions in a first genetic sequence differ from corresponding one or more bases positioned in a reference genetic sequence. The first genetic sequence is a genetic sequence of the client. Sensor data is obtained that provides an indication of one or more characteristics of a current or past environment of the client. The genetic-variant data and the sensor data is processed to generate a disease-risk metric corresponding to a predicted risk of the client developing a particular disease. A communication is generated that is indicative of the disease-risk metric. The communication is transmitted to a remote device.
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公开(公告)号:US20250005110A1
公开(公告)日:2025-01-02
申请号:US18882211
申请日:2024-09-11
Applicant: Color Health, Inc.
Inventor: Ryan Barrett , Nishant Bhat , Huy Hong , Katsuya Noguchi , Wendy McKennon , Krishna Pant , Taylor Sittler , Othman Laraki , Elad Gil
IPC: G06F18/20 , G06F18/23 , G06Q10/00 , G06Q10/063 , G16B20/10 , G16B20/20 , G16B25/00 , G16B25/10 , G16B30/00 , G16B30/10 , G16B50/00 , G16H10/60 , G16H40/67 , H01L21/768
Abstract: Genetic-variant data is obtained that corresponds to one or more variants associated with a client. Each of the one or more variants corresponds to an instance of one or more bases positioned at one or more first positions in a first genetic sequence differ from corresponding one or more bases positioned in a reference genetic sequence. The first genetic sequence is a genetic sequence of the client. Sensor data is obtained that provides an indication of one or more characteristics of a current or past environment of the client. The genetic-variant data and the sensor data is processed to generate a disease-risk metric corresponding to a predicted risk of the client developing a particular disease. A communication is generated that is indicative of the disease-risk metric. The communication is transmitted to a remote device.
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公开(公告)号:US11361842B1
公开(公告)日:2022-06-14
申请号:US17394181
申请日:2021-08-04
Applicant: Color Health, Inc.
Inventor: Ryan Barrett , Nishant Bhat , Huy Hong , Katsuya Noguchi , Wendy McKennon , Krishna Pant , Taylor Sittler , Othman Laraki , Elad Gil
IPC: G16B25/00 , G06K9/62 , G06K9/00 , G16H10/60 , H01L21/768 , G06Q10/00 , G16B20/20 , G16B50/00 , G06Q10/06 , G16H40/67 , G16B30/00 , G16B25/10 , G16B20/10 , G16B30/10
Abstract: Techniques are provided for detecting copy number variations. Each sequence read of a set of sequence reads is aligned with a portion of a reference sequence. A coverage vector is generated that includes a plurality of elements, each element in the plurality of elements indicating a number of the set of sequence reads that were aligned to a particular position within the reference sequence. A normalization vector is accessed that was generated based on performance of a component analysis on a set of other coverage vectors corresponding to a set of other subjects. An adjusted coverage vector is generated using the coverage vector and normalization vector. One or more subject-specific normalization values are generated based on the coverage vector. One or more copy number variations are identified that corresponding to the sample using the adjusted coverage vector and the subject-specific normalization values.
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公开(公告)号:US12099579B1
公开(公告)日:2024-09-24
申请号:US18474868
申请日:2023-09-26
Applicant: Color Health, Inc.
Inventor: Ryan Barrett , Nishant Bhat , Huy Hong , Katsuya Noguchi , Wendy McKennon , Krishna Pant , Taylor Sittler , Othman Laraki , Elad Gil
IPC: G06Q10/00 , G06F18/20 , G06F18/23 , G16B20/20 , G16B25/00 , G16H10/60 , H01L21/768 , G06Q10/063 , G16B20/10 , G16B25/10 , G16B30/00 , G16B30/10 , G16B50/00 , G16H40/67
CPC classification number: G06F18/285 , G06F18/23 , G06Q10/00 , G16B20/20 , G16B25/00 , G16H10/60 , H01L21/76886 , G06F2218/00 , G06Q10/063 , G16B20/10 , G16B25/10 , G16B30/00 , G16B30/10 , G16B50/00 , G16H40/67 , H01L21/768
Abstract: Genetic-variant data is obtained that corresponds to one or more variants associated with a client. Each of the one or more variants corresponds to an instance of one or more bases positioned at one or more first positions in a first genetic sequence differ from corresponding one or more bases positioned in a reference genetic sequence. The first genetic sequence is a genetic sequence of the client. Sensor data is obtained that provides an indication of one or more characteristics of a current or past environment of the client. The genetic-variant data and the sensor data is processed to generate a disease-risk metric corresponding to a predicted risk of the client developing a particular disease. A communication is generated that is indicative of the disease-risk metric. The communication is transmitted to a remote device.
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公开(公告)号:US11120369B2
公开(公告)日:2021-09-14
申请号:US16919351
申请日:2020-07-02
Applicant: Color Health, Inc.
Inventor: Ryan Barrett , Nishant Bhat , Huy Hong , Katsuya Noguchi , Wendy McKennon , Krishna Pant , Taylor Sittler , Othman Laraki , Elad Gil
Abstract: Techniques, systems, and products for analyzing sparse indicators and sensor data and generating communications are disclosed. The sensors may be associated with or incorporated into devices that may automatically relay sensor data for use in analyses and communication generation.
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