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Contig Assembly and More!
SnapGene 4.3 adds multiple new features including contig assembly, more flexible alignment tools, support for nicking endonucleases, and support for point features.
 

Contig Assembly

Linear or circular contigs can be assembled de novo from overlapping sequences or Sanger sequence traces.
Contig Assembly


Flexible Alignments

Sequences to be aligned can now be imported in various ways. A portion of a multiple alignment can be extracted to generate a new multiple alignment, or an existing multiple alignment can be edited to add or remove alignments generated by different algorithms.
Flexible Alignments


Nicking Enzymes

Nicking endonucleases can be displayed. When a selection spans from an end of a linear sequence to a nicking endonuclease site, that single-stranded region can be removed by pressing Delete.
Nicking Enzymes


Point Features

Zero-length point features are now supported for DNA sequences, and are recognized when importing files from GenBankMacVector, or Gene Construction Kit.
Point Features


Enzyme Site Highlighting

Commonly used enzyme sites can be highlighted in gold for quick identification.
Enzyme Site Highlighting


Alignment Consensus Enhancements

Consensus sequences for multiple alignments have an improved format, and can now be copied or exported.
lignment Consensus Enhancements


Stored Edits for Alignment to a Reference Sequence

By popular demand, when an alignment to a reference DNA sequence is edited by adjusting the endpoints of the aligned sequences, those edits are preserved and restored.
Stored Edits for Alignment to a Reference Sequence


Feature Import from Other File Formats

Features can be imported into a DNA sequence from BED, GFF3, or GTF formats.
Feature Import from Other File Formats


Import from UniProt

Protein sequence records can be imported from the UniProt database.
Import from UniProt


Import of Genome Compiler Projects

Genome Compiler project files (.gcproj) can now be opened directly in SnapGene. For construction project files, the construction histories are captured in History view.
Import of Genome Compiler Projects


Primer Addition Dates

When a primer is added to a file, the date is recorded. Primers can be sorted by Date Added.
Primer Addition Dates

 


Reading and Writing Alignment File Formats

SnapGene can import alignments to a reference sequence in SAM/BAM and Vector NTI® .cep formats, and can export alignments to a reference sequence in SAM/BAM formats.

 

Exciting developments and partnerships are in the pipeline for 2019. Please stay tuned!


As always, if you have feedback or your own wish list, we want to hear from you.
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