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公开(公告)号:EP2971132B1
公开(公告)日:2020-05-06
申请号:EP14764952.9
申请日:2014-03-17
发明人: GOEL, Ajay , HUR, Keun , TOIYAMA, Yuji , BOLAND, Richard C.
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公开(公告)号:EP3218511B1
公开(公告)日:2020-04-22
申请号:EP15793823.4
申请日:2015-11-11
发明人: GUNDERSON, Kevin L. , BAI, Jingwei , KELLINGER, Matthew William , BEIERLE, John M. , BOUTELL, Jonathan Mark , RIGATTI, Roberto , ROGERT BACIGALUPO, Maria Candelaria , BOYANOV, Boyan , MAISINGER, Klaus
IPC分类号: C12Q1/6874 , B01J19/00 , C40B40/06 , C40B50/14
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公开(公告)号:EP3597772A1
公开(公告)日:2020-01-22
申请号:EP19179386.8
申请日:2014-04-17
IPC分类号: C12Q1/68 , C40B40/06 , C40B50/06 , C12Q1/6869 , C12N15/10
摘要: The present invention provides an approach to increase the effective read length of commercially available sequencing platforms to several kilobases and be broadly applied to obtain long sequence reads from mixed template populations. A method for generating extended sequence reads of long DNA molecules in a sample, comprising the steps of: assigning a specific barcode sequence to each template DNA molecule in a sample to obtain barcode-tagged molecules; amplifying the barcode-tagged molecules; fragmenting the amplified barcode-tagged molecules to obtain barcode-containing fragments; juxtaposing the barcode-containing fragments to random short segments of the original DNA template molecule during the process of generating a sequencing library to obtain demultiplexed reads; and assembling the demultiplexed reads to obtain extended sequence reads for each DNA template molecule, is disclosed.
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公开(公告)号:EP2734621B1
公开(公告)日:2019-09-04
申请号:EP12845790.0
申请日:2012-07-22
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公开(公告)号:EP3519571A1
公开(公告)日:2019-08-07
申请号:EP17857297.0
申请日:2017-09-27
发明人: WANG, Jinpeng , YANG, Qin , FERGUSON, Brian Scott , GONG, Qiang
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36.
公开(公告)号:EP3204518B1
公开(公告)日:2019-07-10
申请号:EP15849044.1
申请日:2015-10-08
申请人: Invitae Corporation
发明人: OLIVARES, Eric
IPC分类号: C12Q1/68 , C12Q1/6806 , C12Q1/6809 , C12Q1/6832 , C12Q1/6853 , C12Q1/6858 , C12Q1/686 , C12Q1/6874 , C12Q1/6883 , C40B30/04 , C40B40/06 , C40B70/00 , C40B40/08
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公开(公告)号:EP2781599B1
公开(公告)日:2019-05-08
申请号:EP12850348.9
申请日:2012-11-15
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公开(公告)号:EP3443149A1
公开(公告)日:2019-02-20
申请号:EP17781661.8
申请日:2017-04-13
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公开(公告)号:EP3411517A1
公开(公告)日:2018-12-12
申请号:EP17746659.6
申请日:2017-02-06
发明人: WANG, Jean , DICK, John , NG, Stanley , MINDEN, Mark , MITCHELL, Amanda , CHEN, Weihsu, Claire , ZANDSTRA, Peter , KENNEDY, James
CPC分类号: G01N33/57426 , C12Q1/6883 , C12Q2600/106 , C12Q2600/118 , C12Q2600/158 , C40B40/06 , C40B40/08 , G01N2800/52 , G06F19/10 , G06F19/20
摘要: There is described herein a method of prognosing or classifying a subject with acute myeloid leukemia (AML) comprising: (a) determining the expression level of at least 3 genes in a test sample from the subject selected from the group consisting of DNMT3B, ZBTB46, NYNRIN, ARHGAP22, LAPTM4B, MMRN1, DPYSL3, KIAAQ125. CDK6, CPXM1, SOCS2, SMIM24, EMP1, NGFRAP1, CD34, AKR1C3, GPR56; and (b) comparing expression of the at least 3 genes in the test sample with reference expression levels of the at least 3 genes from control samples from a cohort of patients; wherein a difference or similarity in the expression of the at least 3 genes in the test sample and the reference expression levels is used to prognose or classify the subject with AML into a low risk group or a high risk group for worse survival.
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公开(公告)号:EP3408412A1
公开(公告)日:2018-12-05
申请号:EP17743495.8
申请日:2017-01-27
发明人: JENKINS, Mark , BUCHANAN, Daniel , HOPPER, John L.
CPC分类号: C12Q1/6886 , C12Q2600/156 , C40B40/06
摘要: The present disclosure relates to methods and systems for assessing the risk of a human subject for developing colorectal cancer. These methods may be combined with the subjects clinical risk to improve risk analysis. Such methods may be used to assist decision making about appropriate colorectal cancer screening regimens.
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