Bibliographic Details
Title: |
Long-read individual-molecule sequencing reveals CRISPR-induced genetic heterogeneity in human ESCs |
Authors: |
Chongwei Bi, Lin Wang, Baolei Yuan, Xuan Zhou, Yu Li, Sheng Wang, Yuhong Pang, Xin Gao, Yanyi Huang, Mo Li |
Source: |
Genome Biology, Vol 21, Iss 1, Pp 1-14 (2020) |
Publisher Information: |
BMC, 2020. |
Publication Year: |
2020 |
Collection: |
LCC:Biology (General) LCC:Genetics |
Subject Terms: |
Human embryonic stem cell, CRISPR-Cas9, Genome editing, Nanopore sequencing, Long-read sequencing, Next-generation sequencing, Biology (General), QH301-705.5, Genetics, QH426-470 |
More Details: |
Abstract Quantifying the genetic heterogeneity of a cell population is essential to understanding of biological systems. We develop a universal method to label individual DNA molecules for single-base-resolution haplotype-resolved quantitative characterization of diverse types of rare variants, with frequency as low as 4 × 10−5, using both short- or long-read sequencing platforms. It provides the first quantitative evidence of persistent nonrandom large structural variants and an increase in single-nucleotide variants at the on-target locus following repair of double-strand breaks induced by CRISPR-Cas9 in human embryonic stem cells. |
Document Type: |
article |
File Description: |
electronic resource |
Language: |
English |
ISSN: |
1474-760X |
Relation: |
http://link.springer.com/article/10.1186/s13059-020-02143-8; https://doaj.org/toc/1474-760X |
DOI: |
10.1186/s13059-020-02143-8 |
Access URL: |
https://doaj.org/article/8ac7efe6f33542c18c341407186c7d78 |
Accession Number: |
edsdoj.8ac7efe6f33542c18c341407186c7d78 |
Database: |
Directory of Open Access Journals |