SnapGene automatically generates a record of every sequence edit and cloning procedure, so you won’t lose track of how a construct was made, even after a lab member leaves. Identify open reading frames (ORFs) with a single mouse click.Įxport a plasmid map as an image, or export an annotated DNA sequence to GenBank format.įreely share data with your colleagues or customers using the universally accessible SnapGene format. dna files can be opened by the free cross-platform SnapGene Viewer, enabling you to share richly annotated maps and sequences with colleagues. Visualize: Create a DNA sequence file by either entering a sequence, or importing a record from GenBank, or opening an annotated sequence stored in one of many common file formats. Search a DNA sequence to match either a DNA query, or a protein translation, or an annotation.Īutomatically annotate common features, or manually annotate coding sequences and other features.ĭesign and annotate primers for PCR, sequencing, or mutagenesis. SnapGene Viewer allows molecular biologists to create, browse, and share richly annotated DNA sequence files up to 1Gb in length.
(A) Diagram illustrating the positions of the T-DNA inserts in (i) om47-1 (SALK016767) and (ii) om47-2 (GABI369G03) lines of the A.
#Snapgene viewer pdest 17 software
SnapGene Viewer allows molecular biologists to create, browse, and share richly annotated DNA sequence files up to 1Gb in length.Ĭreate a DNA sequence file by either entering a sequence, or importing a record from GenBank, or opening an annotated sequence stored in one of many common file formats.īrowse or print a DNA sequence and its annotations using customizable Map, Sequence, Enzymes, Features, Primers, and History views. Confirmation and characterization of T-DNA insertional knock-out lines for Arabidopsis thaliana OM47. Free software that allows you to create, browse, and share richly annotated sequence files.
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