September 2017
Authors:
Billy Lau and Hanlee Ji
Info:
Scientists aimed to address errors that occur with conventional molecular barcodes for RNA-seq workflows. They developed transposable error-correcting barcodes with tens of billions of unique labels and found that this approach mitigates such problems. They validated the approach in a project that incorporated Pippin Prep to remove PCR products smaller than 500 bp.
Citation:
BMC Genomics 201718:745
doi: 10.1186/s12864-017-4141-4