Ka Thao

ORCID: 0009-0004-5315-6233
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About
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Research Areas
  • RNA and protein synthesis mechanisms
  • CRISPR and Genetic Engineering
  • Chromosomal and Genetic Variations
  • Plant Virus Research Studies

Dana-Farber Cancer Institute
2024

Harvard University
2024

Deciphering the context-specific relationship between sequence and function is a major challenge in genomics. Existing tools for inducing locus-specific hypermutation evolution native genome context are limited. Here we present programmable platform long-range, called helicase-assisted continuous editing (HACE). HACE leverages CRISPR-Cas9 to target processive helicase-deaminase fusion that incurs mutations across large (>1000–base pair) genomic intervals. We applied identify...

10.1126/science.adn5876 article EN Science 2024-10-10

Abstract A major challenge in human genomics is to decipher the context specific relationship of sequence function. However, existing tools for locus hypermutation and evolution native genome are limited. Here we present a novel programmable platform long-range, locus-specific called helicase-assisted continuous editing (HACE). HACE leverages CRISPR-Cas9 target processive helicase-deaminase fusion that incurs mutations across large (>1000 bp) genomic intervals. We applied identify MEK1...

10.1101/2024.02.01.577593 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-02-01
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