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GENOME CAPTURE AND SEQUENCING TO DETERMINE GENOME-WIDE COPY NUMBER VARIATION

机译:基因组捕获和测序以确定全基因组拷贝数变异

摘要

Provided herein is a capture library for target enrichment of sequences of interest from a genome DNA sample. The capture library comprises a plurality of capture oligos tiling a plurality of capture regions evenly-spaced along a genome. Each two adjacent capture regions of the plurality capture regions are separated by a spacing of about 6 to about 14 kilobases in length. The plurality of capture regions has a size of about 150 base pairs in length. Further, each capture oligo of the plurality of capture oligos comprises average 70 nucleotides in length. The capture libraries are suitable for enriching about 150 base pairs region approximately every 10 kilobases in a genome DNA. This capture library can be used to measure replication timing and copy number variation in human pediatric acute lymphocytic leukemia samples, and is also broadly applicable to any CNV application.
机译:本文提供了捕获文库,用于从基因组DNA样品中富集目标序列。捕获文库包括多个捕获寡核苷酸,其将沿着基因组均匀间隔的多个捕获区域平铺。多个捕获区域中的每两个相邻的捕获区域以大约6至大约14千碱基的长度间隔开。多个捕获区域的长度为大约150个碱基对。此外,多个捕获寡核苷酸中的每个捕获寡核苷酸平均长度为70个核苷酸。捕获文库适合于在基因组DNA中大约每10千个碱基富集约150个碱基对区域。该捕获文库可用于测量人类小儿急性淋巴细胞白血病样本中的复制时间和拷贝数变化,并且还广泛适用于任何CNV应用。

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