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    • 3. 发明申请
    • Ribonucleic acid interference molecules and binding sites derived by analyzing intergenic and intronic regions of genomes
    • 通过分析基因组的基因和内含子区域导致的核糖核酸干扰分子和结合位点
    • US20110178283A1
    • 2011-07-21
    • US11408557
    • 2006-04-21
    • Isidore RigoutsosTien HuynhAristotelis TsirigosAlice Carolyn McHardy
    • Isidore RigoutsosTien HuynhAristotelis TsirigosAlice Carolyn McHardy
    • C07H21/02
    • G06F19/22G06F19/18
    • Sequences that can be used in the context of controlled gene regulation are provided. In one aspect, at least one sequence comprising at least one of one or more sequences having SEQ ID NO: 1 through SEQ ID NO: 747,326 is provided. One or more of the provided sequences may be computationally predicted, e.g., from publicly available genomes, using a method based on pattern discovery. In another aspect, a method for regulating the expression of a transcript comprises the step of said transcript containing a region that corresponds to at least one of the provided sequences having SEQ ID NO: 1 through SEQ ID NO: 747,326, the region being targeted either by a naturally occurring, or appropriately designed, interfering RNA molecule that regulates the expression of said transcript through post-transcriptional silencing. In a third aspect, a method for regulating the expression of a transcript comprises the step of at least one of the provided sequences having SEQ ID NO: 1 through SEQ ID NO: 747,326 being used to design an interfering RNA molecule that contains a region that corresponds to the reverse complement of one or more of the one or more sequences having SEQ ID NO: 1 through SEQ ID NO: 747,326, the interfering molecule regulating, through post-transcriptional silencing, one or more transcripts that contain said sequence of the one or more sequences having SEQ ID NO: 1 through SEQ ID NO: 747,326, or a substantial fraction thereof.
    • 提供了可在受控基因调控环境中使用的序列。 在一个方面,提供至少一个包含具有SEQ ID NO:1至SEQ ID NO:747,326的一个或多个序列中的至少一个的序列。 所提供的序列中的一个或多个可以使用基于模式发现的方法从计算上预测,例如来自公众可获得的基因组。 在另一方面,调节转录物表达的方法包括所述转录物的步骤,所述转录物含有对应于至少一个所提供的具有SEQ ID NO:1至SEQ ID NO:747,326的序列的区域,所述区域被靶向 通过天然存在或适当设计的干扰RNA分子,其通过转录后沉默调节所述转录物的表达。 在第三方面,用于调节转录物表达的方法包括提供的具有SEQ ID NO:1至SEQ ID NO:747,326的序列中的至少一个的步骤用于设计干扰RNA分子,所述干扰RNA分子含有 对应于具有SEQ ID NO:1至SEQ ID NO:747,326的一个或多个一个或多个序列的反向互补序列,干扰分子通过转录后沉默调节一个或多个含有所述序列的所述序列的转录本 或更多的具有SEQ ID NO:1至SEQ ID NO:747,326的序列,或其相当一部分。
    • 7. 发明申请
    • System and Method for Identification of MicroRNA Target Sites and Corresponding Targeting MicroRNA Sequences
    • 用于鉴定微小RNA靶位点的系统和方法以及相应的靶向性微RNA序列
    • US20090012720A1
    • 2009-01-08
    • US12135551
    • 2008-06-09
    • Tien HuynhKevin Charles MirandaIsidore Rigoutsos
    • Tien HuynhKevin Charles MirandaIsidore Rigoutsos
    • G06F19/00
    • G06F19/22C12N15/111C12N2310/14C12N2320/11C12N2330/10G06F19/16G06F19/18G06F19/24
    • A method for determining whether a nucleotide sequence contains a microRNA binding site and which microRNA will bind thereto is provided. For example, in one aspect of the invention, a method for determining whether a nucleotide sequence contains a microRNA binding site and which microRNA sequence will bind thereto is comprised of the following steps. One or more patterns are generated by processing a collection of known mature microRNA sequences. The reverse complement of each generated patter is then computed. One or more attributes are then assigned to the reverse complement of the one or more generated patterns. The one or more patterns that correspond to a reverse complement having one or more assigned attributes that satisfy at least one criterion are thereafter subselected. Each subselected pattern is then used to analyze the nucleotide sequence, such that a determination is made whether the nucleotide sequence contains a microRNA binding site and which microRNA sequence will bind thereto.
    • 提供了确定核苷酸序列是否含有微小RNA结合位点以及哪个微小RNA将与其结合的方法。 例如,在本发明的一个方面,确定核苷酸序列是否含有微小RNA结合位点以及哪个微小RNA序列将与其结合的方法包括以下步骤。 通过处理已知的成熟microRNA序列的集合来产生一个或多个图案。 然后计算每个生成的图案的反向补码。 然后将一个或多个属性分配给一个或多个生成的模式的反向补码。 对应于具有满足至少一个标准的一个或多个分配属性的反向补码的一个或多个模式随后被子选择。 然后使用每个子选择图案来分析核苷酸序列,从而确定核苷酸序列是否含有微小RNA结合位点,哪个微小RNA序列将与其结合。
    • 8. 发明申请
    • System and method for identification of MicroRNA target sites and corresponding targeting MicroRNA sequences
    • 用于鉴定MicroRNA靶位点的系统和方法以及相应的靶向MicroRNA序列
    • US20070154896A1
    • 2007-07-05
    • US11351821
    • 2006-02-10
    • Tien HuynhKevin MirandaIsidore Rigoutsos
    • Tien HuynhKevin MirandaIsidore Rigoutsos
    • C12Q1/68G06F19/00
    • G16B30/00C12N15/111C12N2310/14C12N2320/11C12N2330/10G16B15/00G16B20/00G16B40/00
    • A method for determining whether a nucleotide sequence contains a microRNA binding site and which microRNA will bind thereto is provided. For example, in one aspect of the invention, a method for determining whether a nucleotide sequence contains a microRNA binding site and which microRNA sequence will bind thereto is comprised of the following steps. One or more patterns are generated by processing a collection of known mature microRNA sequences. The reverse complement of each generated patter is then computed. One or more attributes are then assigned to the reverse complement of the one or more generated patterns. The one or more patterns that correspond to a reverse complement having one or more assigned attributes that satisfy at least one criterion are thereafter subselected. Each subselected pattern is then used to analyze the nucleotide sequence, such that a determination is made whether the nucleotide sequence contains a microRNA binding site and which microRNA sequence will bind thereto.
    • 提供了确定核苷酸序列是否含有微小RNA结合位点以及哪个微小RNA将与其结合的方法。 例如,在本发明的一个方面,确定核苷酸序列是否含有微小RNA结合位点以及哪个微小RNA序列将与其结合的方法包括以下步骤。 通过处理已知的成熟microRNA序列的集合来产生一个或多个图案。 然后计算每个生成的图案的反向补码。 然后将一个或多个属性分配给一个或多个生成的模式的反向补码。 对应于具有满足至少一个标准的一个或多个分配属性的反向补码的一个或多个模式随后被子选择。 然后使用每个子选择图案来分析核苷酸序列,从而确定核苷酸序列是否含有微小RNA结合位点,哪个微小RNA序列将与其结合。