Charles Hodgens

Postdoctoral Researcher



Using indCAPS to Detect CRISPR/Cas9 Induced Mutations.


Journal article


Charles Hodgens, Z. Nimchuk, J. Kieber
Bio-protocol, 2019

Semantic Scholar DOI PubMed
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Cite

APA   Click to copy
Hodgens, C., Nimchuk, Z., & Kieber, J. (2019). Using indCAPS to Detect CRISPR/Cas9 Induced Mutations. Bio-Protocol.


Chicago/Turabian   Click to copy
Hodgens, Charles, Z. Nimchuk, and J. Kieber. “Using IndCAPS to Detect CRISPR/Cas9 Induced Mutations.” Bio-protocol (2019).


MLA   Click to copy
Hodgens, Charles, et al. “Using IndCAPS to Detect CRISPR/Cas9 Induced Mutations.” Bio-Protocol, 2019.


BibTeX   Click to copy

@article{charles2019a,
  title = {Using indCAPS to Detect CRISPR/Cas9 Induced Mutations.},
  year = {2019},
  journal = {Bio-protocol},
  author = {Hodgens, Charles and Nimchuk, Z. and Kieber, J.}
}

Abstract

Cleaved amplified polymorphic sequences (CAPS) assays are useful tools for detecting small mutations such as single nucleotide polymorphisms (SNPs) or insertion/deletions (indels) present in an amplified DNA fragment. A mutation that disrupts or creates a restriction site will prevent cleavage by a restriction enzyme, allowing discrimination of wild-type and mutant alleles. In cases where no convenient restriction site is present, a derived Cleaved Amplified Polymorphic Sequence (dCAPS) assay can be used, where mismatches in the primer are used to create a diagnostic restriction site. No special design constraints are present for a CAPS assay, but cases where CAPS assays can be used are infrequent. A dCAPS assay can be burdensome to design by hand, but it is more broadly applicable. This protocol will describe the use of the indCAPS tool for the design of CAPS and dCAPS primers. The indCAPS tool was designed to be compatible with indel alleles, which prior tools struggled with but have increased importance since the rise of CRISPR/Cas9 mutagenesis methods.


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