Synthetic mismatches enable specific CRISPR-Cas12a-based detection of genome-wide SNVs tracked by ARTEMIS

Kavish A.V. Kohabir(Amsterdam Neuroscience), Erik A. Sistermans(Amsterdam Neuroscience), Lars O. Nooi(Amsterdam University Medical Centers), Jasper Linthorst(Amsterdam Neuroscience), Rob M.F. Wolthuis(Oncode Institute)
Cell Reports Methods
December 1, 2024
10.1016/j.crmeth.2024.100912
Cited by 14

Related Papers

Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation
|Brain|2002|294
Genomic and molecular characterization of preterm birth
|Proceedings of the National Academy of Sciences|2019|81
The spindle checkpoint, APC/CCdc20, and APC/CCdh1 play distinct roles in connecting mitosis to S phase
|The Journal of Cell Biology|2013|58
Extreme enrichment of VNTR-associated polymorphicity in human subtelomeres: genes with most VNTRs are predominantly expressed in the brain
|Translational Psychiatry|2020|26
The cell‐free DNA virome of 108,349 Dutch pregnant women
|Prenatal Diagnosis|2022|24