Methods, Systems, Compositions, Kits, Apparatus and Computer-Readable Media for Molecular Tagging

    公开(公告)号:US20210363596A1

    公开(公告)日:2021-11-25

    申请号:US17389009

    申请日:2021-07-29

    Abstract: In some embodiments, the disclosure relates generally to methods, as well as related systems, compositions, kits, apparatuses and computer-readable media, comprising a multiplex molecular tagging procedure that employs a plurality of tags that are appended to a plurality of polynucleotides. The tags have characteristics, including a sequence, length and/or detectable moiety, or any other characteristic, that uniquely identifies the polynucleotide molecule to which it is appended, and permits tracking individual tagged molecules in a mixture of tagged molecules. For example, the tag having a unique tag sequence, can uniquely identify an individual polynucleotide to which it is appended, and distinguish the individual polynucleotide from other tagged polynucleotides in a mixture. In some embodiments, the multiplex molecular tagging procedure can be used for generating error-corrected sequencing data and for detecting a target polynucleotide which is present at low abundance in a nucleic acid sample.

    METHODS FOR PARTNER AGNOSTIC GENE FUSION DETECTION

    公开(公告)号:US20200318175A1

    公开(公告)日:2020-10-08

    申请号:US16825238

    申请日:2020-03-20

    Abstract: A method for detecting a gene fusion includes amplifying a nucleic acid sample in the presence of primer pool to produce a plurality of amplicons. The primer pool includes primers targeting a plurality of exon-exon junctions of a driver gene. The amplicons correspond to the exon-exon junctions. The amplicons are sequenced and aligned to a reference sequence. The number of reads corresponding to each amplicon is normalized to give a normalized read count. A baseline correction is applied to the normalized read counts for the amplicons to form corrected read counts. A binary segmentation score is calculated for each corrected read count. A predicted breakpoint for the gene fusion is determined based on the amplicon index corresponding to the maximum absolute binary segmentation score. Gene fusion events may be detected in a partner agnostic manner, i.e. without prior knowledge of the specific fusion partner genes or specific breakpoint information.

    METHODS, SYSTEMS, COMPOSITIONS, KITS, APPARATUS AND COMPUTER-READABLE MEDIA FOR MOLECULAR TAGGING

    公开(公告)号:US20190323091A1

    公开(公告)日:2019-10-24

    申请号:US16503262

    申请日:2019-07-03

    Abstract: In some embodiments, the disclosure relates generally to methods, as well as related systems, compositions, kits, apparatuses and computer-readable media, comprising a multiplex molecular tagging procedure that employs a plurality of tags that are appended to a plurality of polynucleotides. The tags have characteristics, including a sequence, length and/or detectable moiety, or any other characteristic, that uniquely identifies the polynucleotide molecule to which it is appended, and permits tracking individual tagged molecules in a mixture of tagged molecules. For example, the tag having a unique tag sequence, can uniquely identify an individual polynucleotide to which it is appended, and distinguish the individual polynucleotide from other tagged polynucleotides in a mixture. In some embodiments, the multiplex molecular tagging procedure can be used for generating error-corrected sequencing data and for detecting a target polynucleotide which is present at low abundance in a nucleic acid sample.

    OLIGONUCLEOTIDES AND METHODS FOR THE PREPARATION OF RNA LIBRARIES
    5.
    发明申请
    OLIGONUCLEOTIDES AND METHODS FOR THE PREPARATION OF RNA LIBRARIES 有权
    寡核苷酸和制备RNA文库的方法

    公开(公告)号:US20140128291A1

    公开(公告)日:2014-05-08

    申请号:US13774648

    申请日:2013-02-22

    Abstract: Disclosed are compositions and methods for the preparation of RNA libraries for sequencing, gene expression profiling, microarray and other uses and for simplification of the library preparation process. The disclosure provides blocking oligonucleotides which bind to byproduct nucleic acid molecules formed during the ligation of adapters to nucleic acid segments prior to sequencing and inhibit or block amplification of the byproduct nucleic acid molecules in subsequent amplification reactions. Methods for library preparation using blocking oligonucleotides are also provided.

    Abstract translation: 公开了用于制备用于测序,基因表达谱,微阵列和其他用途的RNA文库以及简化文库制备过程的组合物和方法。 本公开内容提供了阻断寡核苷酸,其结合在连接核酸片段的衔接子之前形成的副产物核酸分子,并在随后的扩增反应中抑制或阻断副产物核酸分子的扩增。 还提供了使用封闭寡核苷酸的文库制备方法。

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