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.
BAM haplotype filtering
Step 1: Copy BAM file URL
Copy the sample BAM file URL address.
Click the Open command in the File menu.
Select BAM/CSRA files tab.
Paste the BAM file URL address into the Genome Workbench Open dialog (or just open the Genome Workbench sample file and skip the tutorial steps 1-3).
Click Next>.
Step 2: Map it to assembly GRCh37
Select the Use Mapping check box.
Click the Find Assembly button.
Type "GCF_000001405.13" in the Search term box and click the Find Assemblies button.
Select the row with the desired accession in the search results.
Click OK button.
Click Next>.
Step 3: Select Sequence NC_000001.10
Type "NC_000001.10" in the Filter box and press Enter.
Click Next>. Click Finish to create a new project.
Step 4: Open Graphical Sequence View for NC_000001.10
Double-click the NC_000001.10 project item under Data folder in the Project View on the left.
Click the Graphical Sequence View line.
Ignore the warning message by clicking OK.
Step 5: Activate alignment track NA24385_hg19_phased_possorted_bam
Click the Configure Tracks icon.
Type "NA24385_hg19_phased_possorted_bam" in the Search box and press Enter.
Select the track with the same name and click OK.
Step 6: Zoom to a level where individual alignments are displayed (e.g. 19565K-19572K).
Right-click anywhere below the ruler. In the pop-up menu select the Go to Sequence Position/Range command. In the pop-up dialog type in "19565K-19572K" to the Sequence Position/Range box. Click the Go button. Click the Close button to close the dialog.
Step 7: Enable sorting by haplotype:
Click the Content Icon in the right upper corner of the alignment track.
Select the Sort alignments by haplotype command.
The alignment tracks must show 3 subtracks:
Zoom in to the desired level of detail.
For more information on BAM files please see the Working with BAM Files Tutorial, BAM file FAQ section, and Import BAMs video tutorial.
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