Align selected unaligned sequences with an existing alignment.Merge unaligned sequences into an existing alignment.Merge two existing alignments (“Profile alignment”).Troubleshooting “wrong type” or “too long” errors.Search for text or accession number matches (Entrez).Search for disagreements between sequences.Search for nucleotide or residue strings.Search for or within a sequence using a text query.Part F: Export the annotated target sequence.Part A: Add, rename and align sequences.Map features (copy features to another sequence).Reverse complement one or more sequences.Rename sequences automatically using specified data fields.Add sequences from a saved project to an active project.Add only the portion of sequence that corresponds to a feature.Try it! – Add and align multi-segment sequences.Add multi-segment sequences to a project.Add only sequences that meet filtering thresholds.Save the layout and apply it to other projects.Customize the layout of other window components.Customize the appearance and layout of views.When a portion of a pairwise alignment is selected.When a portion of multiple sequences is selected.When a portion of a sequence is selected. When no document, or a blank document, is open.Using the Overview as a sequence navigation tool.Overview after aligning and entering additional sequences.Overview after aligning multiple genomes with Mauve.Overview prior to performing an alignment.Import an alignment from another application.
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