Dna Sequencing
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Mutation Surveyor v.2 60
Mutation Surveyor® is a DNA Sequencing software for the analysis of Sanger sequencing files (.ab1,.RSD,.ESD & .scf) generated by Applied Biosystems Genetic Analyzers, MegaBACE as well as Beckman CEQ electrophoresis systems.
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GATCViewer v.1.0
GATC Viewer for raw data from ABI 3730 xl (Sanger sequencing).This program allows you to display chromatograms in .abi format. DNA sequencing service, Next Generation sequencing, bioinformatics services and sequencing analysis software.
Mallard v.1.02
Sequence analysis made easy. Mallard is a software for screening 16S rRNA clone libraries, and similar multiple sequence alignments for chimeras and other anomalies.The nature of DNA sequencing is such that artifacts are inevitably introduced and,
Sequencher v.4.7
Sequencher is the industry standard software for DNA sequence analysis.
DNASIS MAX v.3.0
MiraiBio DNASIS MAX is a bioinformatics software for DNA/RNA/Amino Acid sequence analysis. DNASIS MAX bioinformatics software helps life scientists edit, annotate and analyze DNA, RNA and amino acid sequences.
BVTech Plasmid(1) v.5.0
BVTech Plasmid is DNA sequence analysis and plasmid drawing software for Windows PCs.
GeneMarker v.2 2
GeneMarker® is a unique genotype analysis software which integrates new technologies enhancing the speed, accuracy and ease of analysis.
Geneious Pro v.5.6.2
Geneious Pro is a software that speeds up and simplifies research in molecular biology and biochemistry. It is a revolutionary bioinformatics program platform that is both ultra-strong and easy-to-use. Scientists,
Geneious Basic v.5.6.4
Geneious Basic is a software that speeds up and simplifies research in molecular biology and biochemistry. Geneious is a useful,
Htk v.3. 4. 2001
The Hidden Markov Model Toolkit (HTK) is a portable toolkit for building and manipulating hidden Markov models.
CodonCode Aligner v.3. 7. 2001
CodonCode Aligner introduced several features and improvements like building Neighbor-Joining trees, zooming in the contig view, shortening reference sequences after alignments, masking contig bases in low coverage regions, the percentange consensus