Support for Genome Workbench will end on March 31 2024. You may still use the application, but supporting documentation will not be available after this date. Read more.
Special rendering for discrepancies between genomic sequence and known RefSeq transcripts/corresponding proteins
In a process of genome annotation known RefSeq transcripts/corresponding proteins are aligned to genomic DNA. Special rendering has been implemented for discrepancies in such alignments.
- mismatched codons are shown in red color
- mismatched nucleotide bases are printed over RNA bar
- mismatched amino-acids are printed over CDS bar
- deletions are shown as dashes '-' inside of RNA bar and CDS bar
- insertions are shown as hourglass-like triangles inside of RNA bar and CDS bar
Special case: ribosomal slippage If translation is known to be effected by ribosomal slippage, frameshifts can be seen as shifted (but not colored) codons and corresponding amino acids.
Please download test files for each example. Open each test file with Genome Workbench and open the Graphical Sequence View (right click - Open New View - Graphical Sequence View).
RefSeq coding region with mismatches, deletion, and insertion in the genomic feature compared to the genomic sequence
Test file: Discrepancies in CDS
RefSeq RNA with insertion, deletion, or mismatch in the genomic feature compared to the genomic sequence
Test file: Discrepancies in RNA
Ribosomal Slippage with -1 frameshift
Test file: Ribosomal Slippage with -1 frameshift
Ribosomal slippage is represented by an extra "joinvisual" shift of the translated sequence.
Note how NP_001120696.2's AAA(K) codon is shifted relative to NP_001103414.2's AAC(N) because of -1 frameshift.
Ribosomal slippage with +1 frameshift
Test file: Ribosomal Slippage with +1 frameshift
Current Version is 3.8.2 (released December 12, 2022)
General
Help
Tutorials
- Basic Operation
- Using Active Objects Inspector
- Configure tracks and track display settings
- Working with Non-Public Data
- Viewing Multiple Alignments and Trees
- Broadcasting
- Genes and Variation
- Generating and Viewing Sequence Overlap Alignment
- Working with BAM Files
- Loading Tabular Data
- Working with VCF Files
- Sequence View Markers
- Opening Projects in Genome Workbench
- Publication quality graphics (PDF/SVG image export)
- Editing in Genome Workbench
- Create Protein Alignments using ProSplign
- GFF-CIGAR export for alignments
- Exporting Tree Nodes to CSV
- Generic Table View
- Running BLAST search against custom BLAST databases
- Using Phylogenetic Tree
- Coloring methods in Multiple Alignment View
- Displaying translation discrepancies
- Searching in Genome Workbench
- Graphical View Navigation and Manipulation
- Using the Text View to Review and Edit a Submission
- BAM haplotype filtering
- Displaying new non-NCBI molecules with annotations
- Creating phylogenetic tree from precalculated multiple alignment
- Creating phylogenetic tree starting from search
- Video Tutorials
General use Manuals
- Tree Viewer Formatting
- Tree Viewer Broadcasting
- Genome Workbench Macro
- Query Syntax in Genome Workbench and Tree Viewer
- Multiple Sequence Aligners
- Running Genome Workbench over X Window System
NCBI GenBank Submissions Manuals
- Table of Contents
- Introduction
- Genome Submission Wizard
- Save Submission File
- Reports
- Import
- Sequences
- Add Features
- Add Publication
- Comments
- Editing Tools