Sequencing by avidity enables high accuracy with low reagent consumption
Sinan ArslaniD, Francisco J. Garcia, Minghao GuoiD, Matthew William Kellinger, Semyon KruglyakiD, Jake A. LeVieux, Adeline Mah, Haosen WangiD, Junhua ZhaoiD, Chunhong ZhouiD, Andrew Altomare, John Bailey, Matthew B. Byrne, Chiting Chang, Steve X. Chen, Byungrae Cho, Claudia N. Dennler, Vivian T. DieniD, Derek Fuller, Ryan Kelley, Omid Khandan, Michael KleiniD, Michael Sukhyun KimiD, Bryan R. LajoieiD, Bill Lin, , Jordan M. Neysmith
Abstract
We present avidity sequencing - a novel sequencing chemistry that separately optimizes the process of stepping along a DNA template and the process of identifying each nucleotide within the template. Nucleotide identification uses multivalent nucleotide ligands on dye-labeled cores to form polymerase-polymer nucleotide complexes bound to clonal copies of DNA targets. These polymer-nucleotide substrates, termed avidites, decrease the required concentration of reporting nucleotides from micromolar to nanomolar, and yield negligible dissociation rates. We demonstrate the use of avidites as a key component of a sequencing technology that surpasses Q40 accuracy and enables a diversity of applications that include single cell RNA-seq and whole human genome sequencing. We also show the advantages of this technology in sequencing through long homopolymers.
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