Batch ABI/SCF Sequences Assembler is easy to use software for simple and batch DNA sequence assembly, DNA sequence analysis, contig editing, metadata integration and mutation detection. http://www.dna-assembly.com
Batch ABI/SCF Sequences Assembler is easy to use software for simple and batch DNA sequence assembly, DNA sequence analysis, contig editing, metadata integration and mutation detection. It also offers a powerful chromatogram viewer/editor. The truly user-friendly interface makes Batch ABI/SCF Sequences Assembler the best choice for DNA contig assembly.
Why is Batch ABI/SCF Sequences Assembler special?
The sequence assembly tool offered by the program is complete. You can import and align multiple DNA sequences to a reference sequence. The supported input formats are: SCF, ABI, AB, AB1, AB!, FASTA, SEQ, GBK, TXT, multiFASTA. The chromatogram viewer/editor is really good and easy to use. With a single click any chromatogram can be reverse-complemented. Ambiguities are very easy to spot in the sequence assembly viewer because they are clearly marked in red. There are tow buttons that allows you to jump to the next/previous ambiguity. Bases can be edited/deleted. Low quality ends are not taken into consideration when the contig is created and are marked in dark gray color. The entire alignment can be view at a glance in the contig map viewer.
http://www.dna-assembly.com
Previous Versions
Here you can find the changelog of Batch ABI/SCF Sequences Assembler since it was posted on our website on 2015-04-24 03:00:00.
The latest version is 2.60 and it was updated on 2024-04-22 13:00:21. See below the changes in each version.
Batch ABI/SCF Sequences Assembler version 2.60
Updated At: 2012-04-23
Changes: New: Metadata and batch metadata integration. New: Button to open Windows Explorer in contig's folder, after sequence assembly. New: Remove vectors from single chromatograms. New: SEQUENCE ANALISYS - mark al bases with a confidence level (QV) below a specified threshold, in red.
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