Free in less software for linux

Less 436 is designed as a pager which displays text files, and is often used in command-line environments like the Unix shell and the MS-DOS command prompt to display files.

Major Features:

1. Backwards movement
   • It's hard to believe some people are still using pagers that don't let you move backwards in the file. Even pagers that do let you move backwards often don't work when viewing "standard input"; that is, data that is being piped into the pager from another program.
2. Searching and highlighting
   • Less lets you search for text in the file you're viewing. You can search forwards and backwards. Furthermore, less highlights the text that matches your search, to make it easy to see where the match is.
3. Multiple files
   • Less allows you to switch between any number of different files, remembering your position in each file. You can also do a single search which spans all the files you are working with.
4. Bold and underline
   • Some text files, notably Unix-style "man pages", use overstriking (backspaces) to simulate underlined and bold text. Less interprets this overstriking and displays the text in real underlined or bold mode.
5. Advanced features
   • Less has a large number of fancy features for advanced users. Once you learn the basics, you'll find you can customize less to do almost anything you want it to do. You can change key bindings, set different tab stops, set up filters to view compressed data or other file types, customize the prompt, display line numbers, use "tag" files, and more.
6. Portability
   • Less is available on many different machines, different system architectures, and different terminals. Pretty much wherever you go, you'll find less. You won't have to learn how to use a different pager on every system you use.

DNA BASER - Visit us for updated info: http://www.DNABaser.com

DNA Baser 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 DNA Baser the best choice for DNA contig assembly. For more details, see the DNA BASER Features page.

Why is DNA Baser Assembler special?

Any software company pretends that their product is the best. But lets see for real if DNA Baser can offer you a better proposition. As you will see below we concentrate on adding automatic and batch functions to our product in order to decrease the time. Additional to this, DNA Baser is available at a "kill your competition" price.

Forget about manually trimming the low quality ends of your sequences. DNA Baser Assembler will do it for you!

Do you think you need weeks to assemble hundreds of contigs? What about doing this in minutes? DNA Baser is the only software that can automatically detect and assemble sequences belonging to the same contig based on their filename.

Do you think that is necessary to spend more than 20 minutes to correct discrepancies and mismatches in every contig? Wrong! DNA Baser is the first software which can make correct suggestions in at least 98% of cases.

Have you ever wondered how others laboratories afford to have sequence assembly software in EVERY computer? Simple! They dont spend thousands of dollars for each license. They use DNA Baser Assembler. DNA Baser is affordable, has no annual maintenance fees, technical support is included in price and you have instant access to your key, right after purchase.

You dont have to fill in and submit forms in order to get a trial version. If you want to try it, you can download and install it in less than one minute. No personal data or registration process is required. The trial version is fully functional.

DNA BASER Assembler offers a smart navigation system that takes you to the location of each sequence ambiguity / mutation with a single click.

New: Metadata and batch metadata integration.
New: Button to open Windows Explorer in contigs 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.
New: Batch convert from chromatogram to Fasta with vector removal and automatic metadata integration.
New: Resizable chromatograms.
Full support for low quality sample ends editing.
100% compatible with Mac via Parallels/Bootcamp/VMWare.
Improved handling of corrupted/invalid ABI/SCF files.
Improved contig editor.
Improved file association.
Improved Assemble to reference.
Improved log window.
Improved file handling: Before starting the contig, check if all files in the JobList are valid. Invalid samples are automatically removed from Job List so the assembly process can continue without human intervention. Build a list of invalid files and report it.
Improved user interface: new toolbar, improved embedded help, interactive help, workflow...
Improved sample viewer: Mark as trusted/un-trusted can now be used also in Sample viewer window
New: Show error message while trying to open empty/invalid FASTA files
Improved: Correctly handle multiple contigs resulted when assembling to a reference.
Improved: menu Save as Fasta/Seq/Scf was replaced with Save all as... and Save selected as.... Now the user can choose where to save the file.

Batch assembly. Thousand of contigs can be assembled at once.