CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) genome editing is a revolutionary method in which a programmable RNA targets a nuclease (eg, Cas9) to a specific location in the genome.1,2 The speed, simplicity, and precision with which CRISPR-Cas9 technology enables genetic elements to be mutated, silenced, induced, or replaced has resulted in its widespread adoption in the global research community.
Integrating CRISPR genome editing with the informational power of next-generation sequencing (NGS) enables researchers to have control throughout their editing experiment, resulting in a better understanding of the biological systems they are modifying. NGS may be utilized at various stages of a genome editing workflow, from confirming CRISPR knockouts to analyzing off-target effects and assessing the the functional impact of gene edits.
Applications of CRISPR-Cas9 technology have been identified in the fields of basic and clinical research, therapeutics, drug development, agriculture, and the environment. Clinical research has shown potential utilization for CRISPR in such diseases as sickle cell disease, cancer, AIDS, Huntington’s disease, Duchenne muscular dystrophy, and more.
CRISPR genome editing enables researchers to create genetically modified cell lines and animal models with speed and precision. In addition to creating gene knockouts and gene knock-ins, researchers can use CRISPR technology to modulate gene expression via interference (CRISPRi) or activation (CRISPRa), without altering the genomic sequence (view table).
CRISPR genome editing experiments result in mixed cell populations, with only a small subset carrying the desired edit. Researchers need to determine which cells have the desired CRISPR knockout or targeted mutation. Current methods to evaluate edits involve cleavage assays, PCR, Sanger sequencing, and NGS (view table).
NGS is the only assay that provides both qualitative and quantitative information at high resolution across the full range of modifications, meets the needs of any throughput, and can be used to monitor off-target effects.7 NGS-based targeted sequencing provides a cost-effective solution for confirming CRISPR-induced edits by focusing on regions targeted for modification.Learn more about targeted sequencing
Successful implementation of CRISP/Cas9 technology should include strategies to identify and reduce off-target effects, or unintended modifications at sites other than the intended target. Computational methods to evaluate RNA specificity and predict off-target sites are commonly used during genome editing experiments.
Online tools and web-based algorithms are publicly available (view table). However, genome-wide analyses such as NGS-based whole-genome sequencing (WGS) may be necessary to discover off-target sites that may escape prediction algorithms.8Learn more about WGS
Dr. Sam Sternberg, Assistant Professor at Columbia University, discusses the biology and impact of CRISPR and genome editing.Listen Now
The Illumina Scientific Affairs team summarizes key publications on applications of CRISPR-Cas9 technology.View Video
In this customer interview, a geneticist discusses using NGS in somatic mosacisim studies and possible future applications of CRISPR technology.Read Interview
Screen cell populations after CRISPR modification to determine the gene-regulatory impact of many genes in parallel in thousands of individual cells.
Assess the impact of mutations on the transcriptome as a whole or on the expression of genes/gene families.
Determine the impact of mutations on DNA-protein binding.
Investigate the downstream impact of mutations on methylation status and chromatin remodeling.
In addition to high resolution on- and off-target assessment and functional analysis of CRISPR edits, NGS can be incorporated at additional stages of the CRISPR genome editing workflow.
During the initial design phase, resequencing of a locus or genome (for species that lack a reference genome) can aid in RNA selection. During the process of cloning CRISPR-Cas9/guide RNA constructs, resequencing of the resulting plasmids can provide rapid and high-confidence verification of the CRISPR delivery vectors, especially for high-throughput experiments with large plasmid libraries.
Francis deSouza, President and CEO of Illumina, Inc., took the stage at Aspen Ideas: Health in Colorado to educate the audience on the impact genomics is having across healthcare, and the urgency in bringing its benefits to more people, more quickly.Read Article
The simplicity and low cost of CRISPR-Cas9 technology can extend gene editing in crops from large commodity species to a wider variety of agriculturally important species.Learn more about agrigenomics
The speed and simplicity of CRISPR-Cas9 technology can enable development of new cancer models and discovery of new immunotherapeutic targets and strategies.Learn more about cancer research
The precision of CRISPR-Cas9 genome editing can enable development of cell and animal models of human complex diseases to investigate disease pathology.Learn more about complex disease research
The speed, simplicity, and low cost of CRISPR-Cas9 gene editing has revolutionized cell and molecular biology in the development of gene knockouts and transgenic models.Learn more about cellular and molecular biology research