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公开(公告)号:US10443100B2
公开(公告)日:2019-10-15
申请号:US15358390
申请日:2016-11-22
发明人: Daniel R. Salomon , John Friedewald , Sunil Kurian , Michael M. Abecassis , Steve Head , Phillip Ordoukhanian
摘要: By a genome-wide gene analysis of expression profiles of over 50,000 known or putative gene sequences in peripheral blood, the present inventors have identified a consensus set of gene expression-based molecular biomarkers associated with subclinical acute rejection (subAR). These genes sets are useful for diagnosis, prognosis, monitoring of subAR.
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公开(公告)号:US20170137885A1
公开(公告)日:2017-05-18
申请号:US15358390
申请日:2016-11-22
发明人: Daniel R. Salomon , John Friedewald , Sunil Kurian , Michael M. Abecassis , Steven Head , Phillip Ordoukhanian
IPC分类号: C12Q1/68
CPC分类号: C12Q1/6883 , C12Q2537/165 , C12Q2600/106 , C12Q2600/112 , C12Q2600/118 , C12Q2600/158 , G16B20/00 , G16B25/10 , G16B40/20 , G16B40/30 , G16H50/20 , G16H50/30 , Y02A90/26
摘要: By a genome-wide gene analysis of expression profiles of over 50,000 known or putative gene sequences in peripheral blood, the present inventors have identified a consensus set of gene expression-based molecular biomarkers associated with subclinical acute rejection (subAR). These genes sets are useful for diagnosis, prognosis, monitoring of subAR.
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公开(公告)号:US12060611B2
公开(公告)日:2024-08-13
申请号:US16569119
申请日:2019-09-12
发明人: Daniel Salomon , John Friedewald , Sunil Kurian , Michael M. Abecassis , Steve Head , Phillip Ordoukhanian
IPC分类号: C12Q1/68 , C12Q1/6883 , G16B20/00 , G16B40/20 , G16B40/30 , G16H20/40 , G16H50/20 , G16H50/30 , G16B25/10
CPC分类号: C12Q1/6883 , G16B20/00 , G16B40/20 , G16B40/30 , G16H20/40 , G16H50/20 , G16H50/30 , C12Q2537/165 , C12Q2600/106 , C12Q2600/112 , C12Q2600/118 , C12Q2600/158 , G16B25/10 , Y02A90/10
摘要: By a genome-wide gene analysis of expression profiles of over 50,000 known or putative gene sequences in peripheral blood, the present inventors have identified a consensus set of gene expression-based molecular biomarkers associated with subclinical acute rejection (subAR). These genes sets are useful for diagnosis, prognosis, monitoring of subAR.
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公开(公告)号:US20200208217A1
公开(公告)日:2020-07-02
申请号:US16569119
申请日:2019-09-12
发明人: Daniel Salomon , John Friedewald , Sunil Kurian , Michael M. Abecassis , Steve Head , Phillip Ordoukhanian
摘要: By a genome-wide gene analysis of expression profiles of over 50,000 known or putative gene sequences in peripheral blood, the present inventors have identified a consensus set of gene expression-based molecular biomarkers associated with subclinical acute rejection (subAR). These genes sets are useful for diagnosis, prognosis, monitoring of subAR.
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公开(公告)号:US10968536B2
公开(公告)日:2021-04-06
申请号:US15553495
申请日:2016-02-25
摘要: Methods, compositions and kits are provided herein for insertional modification of nucleic acids by, for example transposase-mediated covalent insertion of insertion sequence into a sample nucleic acid molecule. Using sequence of the insertion to direct amplification of adjacent nucleic acid sequence, and using bar codes to map amplified sequence to partitions, one can map sample nucleic acid sequence to single molecules of the nucleic acid sample that are derived directly from the sample nucleic acid molecule.
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公开(公告)号:US20180237950A1
公开(公告)日:2018-08-23
申请号:US15553495
申请日:2016-02-25
IPC分类号: C40B40/08
CPC分类号: C40B40/08 , C12N15/1093
摘要: Methods, compositions and kits are provided herein for insertional modification of nucleic acids by, for example transposase-mediated covalent insertion of insertion sequence into a sample nucleic acid molecule. Using sequence of the insertion to direct amplification of adjacent nucleic acid sequence, and using bar codes to map amplified sequence to partitions, one can map sample nucleic acid sequence to single molecules of the nucleic acid sample that are derived directly from the sample nucleic acid molecule.
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公开(公告)号:US20210164128A1
公开(公告)日:2021-06-03
申请号:US17172029
申请日:2021-02-09
摘要: Methods, compositions and kits are provided herein for insertional modification of nucleic acids by, for example transposase-mediated covalent insertion of insertion sequence into a sample nucleic acid molecule. Using sequence of the insertion to direct amplification of adjacent nucleic acid sequence, and using bar codes to map amplified sequence to partitions, one can map sample nucleic acid sequence to single molecules of the nucleic acid sample that are derived directly from the sample nucleic acid molecule.
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