All nucleic acid detection assays are designed by ADAPT (manuscript in preparation) to be:
Background and more information, including a protocol, are available on bioRxiv.
Each design option consists of RPA primers and LwaCas13a crRNAs. The crRNAs (not primers) are designed to be specific because these perform the detection. These design options are generated computationally and fully automatically. We have not experimentally validated them, except for one SARS-CoV-2 assay on synthetic targets. They are intended for research-use only.
Select one or multiple taxa below for a single assay or multiplex panel.
Taxonomies here (except SARS-CoV-1 and SARS-like) are based on NCBI's Taxonomy Database, which itself is kept up-to-date with ICTV taxonomy. Genomic data from NCBI's GenBank informed all of these designs, and data from GISAID informed the SARS-CoV-2 designs. All of these designs rely heavily on sequencing that other groups have performed and the genomes they have shared, and we are thankful to them for sharing data.
This was created by Hayden Metsky in collaboration with others from the Sabeti lab. Please email email@example.com with questions or comments.