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UBC Sequencing and Bioinformatics Consortium Webinar: Getting the Most from Sanger Sequencing
November 3, 2021 at 1:00 pm - 2:00 pm
Sanger sequencing, named after two time Nobel Laureate Frederick Sanger, is a quick and inexpensive method for determining the nucleotide sequence of DNA.
Used across a wide range of discipline, Sanger Sequencing can identify single nucleotide polymorphisms, verify a cloned plasmid insert, identify unknown bacterial isolates, confirm next-generation sequencing (NGS) variants, or study a small subset of genes.
Join UBC’s Sequencing and Bioinformatics Consortium on to learn more about the potential role of Sanger Sequencing in your research, tips on preparing samples, troubleshooting and analyzing your data.