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公开(公告)号:US09944977B2
公开(公告)日:2018-04-17
申请号:US14568923
申请日:2014-12-12
发明人: Darren R. Link , Michael Samuels
CPC分类号: C12Q1/6844 , C12Q1/6858 , C12Q2535/122 , C12Q2563/159 , C12Q2563/179 , C12Q2565/629
摘要: The invention generally relates to methods for distinguishing a rare genetic variation in a nucleic acid sequence.
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公开(公告)号:US20150167066A1
公开(公告)日:2015-06-18
申请号:US14568923
申请日:2014-12-12
发明人: Darren R. Link , Michael Samuels
IPC分类号: C12Q1/68
CPC分类号: C12Q1/6844 , C12Q1/6858 , C12Q2535/122 , C12Q2563/159 , C12Q2563/179 , C12Q2565/629
摘要: The invention generally relates to methods for distinguishing a rare genetic variation in a nucleic acid sequence.
摘要翻译: 本发明一般涉及区分核酸序列中罕见遗传变异的方法。
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公开(公告)号:US20170028365A1
公开(公告)日:2017-02-02
申请号:US15290378
申请日:2016-10-11
发明人: Darren Link , Brian Hutchison , Michael Samuels , Michael Weiner
CPC分类号: B01F3/0807 , B01F5/0646 , B01F5/0653 , B01F13/0062 , B01F2215/0037 , B01J19/0046 , B01J2219/00286 , B01J2219/00351 , B01J2219/00418 , B01J2219/00479 , B01J2219/00576 , B01J2219/00585 , B01J2219/0059 , B01J2219/00592 , B01J2219/00599 , B01J2219/0065 , B01J2219/00657 , B01J2219/00664 , B01J2219/00702 , B01J2219/0072 , B01J2219/00722 , B01J2219/0074 , B01J2219/00743 , B01L3/502761 , B01L7/52 , B01L2200/027 , B01L2300/0636 , B01L2300/0645 , B01L2300/0654 , B01L2300/0681 , B01L2300/0864 , B01L2300/0867 , B01L2400/0415 , B01L2400/0487 , C40B40/04 , C40B50/08 , G01N15/1459 , G01N33/5008 , G01N2015/1006 , G01N2500/00 , Y02A90/26
摘要: The present invention generally relates to droplet libraries and to systems and methods for the formation of libraries of droplets. The present invention also relates to methods utilizing these droplet libraries in various biological, chemical, or diagnostic assays.
摘要翻译: 本发明一般涉及液滴库以及用于形成液滴库的系统和方法。 本发明还涉及在各种生物,化学或诊断测定中利用这些液滴文库的方法。
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公开(公告)号:US20150099266A1
公开(公告)日:2015-04-09
申请号:US14505974
申请日:2014-10-03
发明人: Michael Samuels , Jeffrey Olson , Darren R. Link
CPC分类号: G16B20/00
摘要: In certain aspects, methods of the invention involve performing modification state specific enzymatic reaction of nucleic acid in a sample, determining a value associated with efficiency of the modification state specific enzymatic reaction based on a control, determining an amount of target nucleic acid in the sample, and normalizing the amount of target nucleic acid based on the efficiency value. Based on the normalized amount of target nucleic acid, the method further includes determining whether the normalized amount of target nucleic acid is indicative of a condition.
摘要翻译: 在某些方面,本发明的方法涉及在样品中进行核酸的修饰状态特异性酶反应,基于对照确定与修饰状态特异性酶促反应的效率相关的值,确定样品中靶核酸的量 ,并根据效率值使目标核酸的量归一化。 基于目标核酸的归一化量,该方法还包括确定目标核酸的归一化量是否指示条件。
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公开(公告)号:US20180100185A1
公开(公告)日:2018-04-12
申请号:US15835697
申请日:2017-12-08
发明人: Michael Samuels
IPC分类号: C12Q1/686
摘要: The invention generally relates to methods for increasing the amount of DNA available for analysis when using partitioned samples and parallel processing. For example, double-stranded DNA can be dissociated into two single-stranded components, and the single strands partitioned into different droplets prior to analysis. The disclosed methods are useful for performing digital PCR analysis on samples where the target DNA is not in abundance, for example when the sample originates from a body fluid or an FFPE sample.
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公开(公告)号:US20160289670A1
公开(公告)日:2016-10-06
申请号:US14874553
申请日:2015-10-05
IPC分类号: C12N15/10 , G01N33/543
CPC分类号: C12N15/1075 , C12Q1/6874 , C40B50/08 , G01N33/5436 , G01N33/58
摘要: The invention provides barcode libraries and methods of making and using them including obtaining a plurality of nucleic acid constructs in which each construct comprises a unique N-mer and a functional N-mer and segregating the constructs into a fluid compartments such that each compartment contains one or more copies of a unique construct. The invention further provides methods for digital PCR and for use of barcode libraries in digital PCR.
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公开(公告)号:US09840734B2
公开(公告)日:2017-12-12
申请号:US14058799
申请日:2013-10-21
发明人: Michael Samuels
IPC分类号: C12Q1/68
CPC分类号: C12Q1/686 , C12Q2527/107 , C12Q2535/131 , C12Q2563/107 , C12Q2563/159 , C12Q2565/629
摘要: The invention generally relates to methods for increasing the amount of DNA available for analysis when using partitioned samples and parallel processing. For example, double-stranded DNA can be dissociated into two single-stranded components, and the single strands partitioned into different droplets prior to analysis. The disclosed methods are useful for performing digital PCR analysis on samples where the target DNA is not in abundance, for example when the sample originates from a body fluid or an FFPE sample.
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公开(公告)号:US20140303005A1
公开(公告)日:2014-10-09
申请号:US14245348
申请日:2014-04-04
发明人: Michael Samuels , Darren R. Link
IPC分类号: C12N15/10
CPC分类号: C12N15/1075 , C12Q1/6806 , C12Q2563/159
摘要: The invention generally relates to rare cell analysis after negative selection.
摘要翻译: 本发明一般涉及阴性选择后的稀有细胞分析。
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公开(公告)号:US20150184256A1
公开(公告)日:2015-07-02
申请号:US14587365
申请日:2014-12-31
IPC分类号: C12Q1/70
CPC分类号: C12Q1/702 , C12Q1/70 , C12Q2563/159
摘要: The invention includes methods for determining the presence of a latent viral population by analyzing an RNA population from the virus with digital techniques, such as digital PCR or by sequencing cDNA produced from the RNA. The invention additional includes methods for determining the presence of latent viral populations by detecting and/or quantifying enzymes that are uniquely associated with the virus, e.g., reverse transcriptases.
摘要翻译: 本发明包括通过使用数字技术(例如数字PCR)或通过测序从RNA产生的cDNA来分析来自病毒的RNA群体来确定潜伏病毒群体的存在的方法。 本发明另外包括通过检测和/或定量与病毒唯一相关的酶(例如逆转录酶)来确定潜伏病毒种群的存在的方法。
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公开(公告)号:US20150126400A1
公开(公告)日:2015-05-07
申请号:US14596949
申请日:2015-01-14
CPC分类号: C12N15/1072 , C12Q1/6827 , C12Q1/6844 , C12Q1/6883 , C12Q1/6886 , C12Q2600/156 , C12Q2525/155 , C12Q2525/161 , C12Q2563/159 , C12Q2563/179 , C12Q2565/629 , C12Q2521/319 , C12Q2521/501 , C12Q2545/101
摘要: The invention generally relates to method for screening for a condition in a subject. In certain embodiments, methods of the invention involve obtaining a pool of nucleic acids from a sample, incubating the nucleic acids with first and second sets of binders, in which the first set binds uniquely to different regions of a target nucleic acid in the pool, the second set binds uniquely to different regions of a reference nucleic acid in the pool, and the first and second sets include different detectable labels, removing unbound binders, detecting the labels, and screening for a condition based upon results of the detecting step.
摘要翻译: 本发明一般涉及用于筛选受试者的病症的方法。 在某些实施方案中,本发明的方法包括从样品中获得核酸库,将核酸与第一组和第二组结合物孵育,其中第一组与第一组结合到泳池中的靶核酸的不同区域, 第二组与泳池中的参考核酸的不同区域唯一地结合,并且第一组和第二组包括不同的可检测标记,去除未结合的结合物,检测标记,以及基于检测步骤的结果筛选病症。
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