28 October 2020 | Features | By Ankit Kankar | firstname.lastname@example.org
About Webinar Sanger sequencing is used to study a small subset of genes linked to a defined phenotype,confirm next-generation sequencing (NGS) variants, detect minor allele fractions down to 5%, or read contiguous sequences up to 1,000 bases. Fragment analysis is a powerful technique with simple, straightforward workflows and used in a wide-range of applications, such as detection of mutations, genotyping, identification of short tandem repeats, and gene expression profiling.
In this webinar, we will discuss
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