DNA SEQUENCING AND EPIGENOME ANALYSIS
    4.
    发明公开
    DNA SEQUENCING AND EPIGENOME ANALYSIS 有权
    DNA-SEQUENZIERUNG UND EPIGENOMANALYSE

    公开(公告)号:EP3027775A4

    公开(公告)日:2017-04-12

    申请号:EP14832389

    申请日:2014-08-01

    Applicant: STC UNM

    Abstract: This disclosure describes, in one aspect, methods for DNA sequencing and performing epigenomic analyses. Generally, the methods include immobilizing a plurality of copies of a DNA molecule on a surface, stretching at least a portion of the immobilized DNA molecules, and sequencing at least a portion of the immobilized, stretched DNA molecules.

    Abstract translation: 在一个方面,本公开描述了用于DNA测序和进行表观基因组分析的方法。 通常,这些方法包括将多个DNA分子拷贝固定在表面上,拉伸至少一部分固定的DNA分子,并对至少一部分固定的,拉伸的DNA分子进行测序。

    SYNTHETIC LONG READ DNA SEQUENCING
    6.
    发明公开
    SYNTHETIC LONG READ DNA SEQUENCING 有权
    SYNTHETISCHE LONG-READ-DNA-SEQUENZIERUNG

    公开(公告)号:EP3055431A4

    公开(公告)日:2017-05-10

    申请号:EP14852570

    申请日:2014-09-24

    Applicant: STC UNM

    Abstract: The disclosure describes a method for sequencing long portions of DNA sequence by assembling a plurality of shorter polynucleotide reads. Generally, The method includes annealing a plurality of primers to a denatured DNA molecule, appending a barcode polynucleotide to the 5′ end of the primer, subjecting the DNA molecules to a plurality of cycles of (1) pooling, (2) dividing, and (3) appending a barcode polynucleotide to the 5′ end of the primer, sequencing the barcode polynucleotides and the genomic DNA, and assembling the short read polynucleotide sequences having identical barcode polynucleotides.

    Abstract translation: 本公开描述了通过组装多个较短的多核苷酸读数对DNA序列的长部分进行测序的方法。 通常,该方法包括将多个引物退火至变性的DNA分子,将条形码多核苷酸附加至引物的5'末端,使DNA分子经历多次(1)合并,(2)分裂和 (3)将条形码多核苷酸附加到引物的5'末端,对条形码多核苷酸和基因组DNA进行测序,并组装具有相同条形码多核苷酸的短读取多核苷酸序列。

    SYNTHETIC LONG READ DNA SEQUENCING

    公开(公告)号:CA2926934A1

    公开(公告)日:2015-04-16

    申请号:CA2926934

    申请日:2014-09-24

    Applicant: STC UNM

    Abstract: The disclosure describes a method for sequencing long portions of DNA sequence by assembling a plurality of shorter polynucleotide reads. Generally, The method includes annealing a plurality of primers to a denatured DNA molecule, appending a barcode polynucleotide to the 5' end of the primer, subjecting the DNA molecules to a plurality of cycles of (1) pooling, (2) dividing, and (3) appending a barcode polynucleotide to the 5' end of the primer, sequencing the barcode polynucleotides and the genomic DNA, and assembling the short read polynucleotide sequences having identical barcode polynucleotides.

    DNA SEQUENCING AND EPIGENOME ANALYSIS

    公开(公告)号:CA2920250A1

    公开(公告)日:2015-02-05

    申请号:CA2920250

    申请日:2014-08-01

    Abstract: This disclosure describes, in one aspect, methods for DNA sequencing and performing epigenomic analyses. Generally, the methods include immobilizing a plurality of copies of a DNA molecule on a surface, stretching at least a portion of the immobilized DNA molecules, and sequencing at least a portion of the immobilized, stretched DNA molecules.

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