Gene codes sequencher faq update#

Gene codes sequencher faq update#

Double-clicking on a sequence trace in the sample pane will update the base and trace panes with the appropriate sequence. Interactive Viewer Features Four Linked Data Windowsįigure 1: The Project Reviewer Report of Mutation Surveyor provides four interactive and hyperlinked views of Sanger sequencing traces in a mutation project.

The viewer is highly interactive, offering linked navigation between four data windows, including links to the sample and mutation electropherogram windows, and mutation report for quick and easy confirmation of variants such as single nucleotide polymorphisms (SNPs), low-frequency variants (somatic, mosaic, heteroplasmic), and homozygous and heterozygous insertion and deletion (indel) events. Viewing and editing variants is also simplified in the Project Reviewer Report, which color codes variants and provides multiple ways to view sequence traces. The Project Reviewer Report of Mutation Surveyor provides a versatile way of grouping and viewing sample files that are aligned to the same reference, including an overlapping view of individual contigs, an overlapping view of all contigs mapping to the same GenBank file, or an overlapping view of sample files associated with a patient identifier. Contig Reference Assembly and Variant Review in Mutation Surveyorįollowing Sanger sequencing trace alignment and automatic detection of variants, Mutation Surveyor software provides a unique contig reference assembly and variant viewer which would negate the need for additional software packages such as Thermo Fisher Scientific SeqScape® Gene Code's Sequencher® or JSI Medical Systems' SEQUENCE PILOT.