Sequencing data analyses

This chapter explains the features in CLC Genomics Workbench for handling data analysis of low-throughput conventional Sanger sequencing data. For analysis of high-throughput sequencing data, please refer to High-throughput sequencing.

This chapter first explains how to trim sequence reads. Next follows a description of how to assemble reads into contigs both with and without a reference sequence. In the final section, the options for viewing and editing contigs are explained.