EMBOSS
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=== Programs === | === Programs === | ||
- | Hundreds of programs (called applications) are collected within | + | Hundreds of programs (called applications) are collected within EMBOSS, covering different biological areas such as: |
- | + | ||
- | + | ||
*Protein motif identification and domain analysis | *Protein motif identification and domain analysis | ||
*Nucleotide sequence pattern analysis | *Nucleotide sequence pattern analysis | ||
+ | *Sequence alignment, | ||
*Presentation tools for publication, | *Presentation tools for publication, | ||
and much more. | and much more. | ||
- | The EMBOSS applications are organized into | + | The EMBOSS applications are organized into groups according to their function (see the [http://bioinfo.ceinge.unina.it/help/emboss/groups.html Application Groups Documentation] for more information). |
Some'' very popular'' applications are: | Some'' very popular'' applications are: | ||
- | *'''pepstats''': | + | *'''pepstats''': Perform several statistics on proteins. |
*'''showfeat''': Show features of a sequence. | *'''showfeat''': Show features of a sequence. | ||
*'''patmatmotifs''': Compares a protein sequence to the PROSITE motif database. | *'''patmatmotifs''': Compares a protein sequence to the PROSITE motif database. | ||
Line 26: | Line 25: | ||
*'''palindrome''': looks for inverted repeats in a nucleotide sequence. | *'''palindrome''': looks for inverted repeats in a nucleotide sequence. | ||
*'''infoseq''': Displays some simple information about sequences. | *'''infoseq''': Displays some simple information about sequences. | ||
- | *'''water''': Smith-Waterman | + | *'''water''': Perform a local alignment of two sequences according to the Smith-Waterman algorithm. |
- | *'''eprimer3''': Picks PCR primers and hybridization oligos. | + | *'''needle''': Perform a global alignment of two sequences according to the Needleman-Wunsch algorithm. |
+ | *'''eprimer3''': Picks PCR primers and hybridization oligos on sequences. | ||
*'''extractseq''': Extract regions from a sequence. | *'''extractseq''': Extract regions from a sequence. | ||
*'''tfscan''': Scans DNA sequences for transcription factors. | *'''tfscan''': Scans DNA sequences for transcription factors. |
Revision as of 18:16, 12 June 2007
Contents |
EMBOSS
EMBOSS at CEINGE
At CEINGE, EMBOSS (verison 3.0) is installed and run on the cluster machine and is highly connected both with the Bioinformatic service and research group activity. For example, it is used for automatic conversion of different sequence databases into suitable formats for other applications, such as BLAST. Moreover, many EMBOSS applications are used for specific sequence analysis in different group research projects.
The complete list of installed EMBOSS applications is available here
Overview
EMBOSS (European Molecular Biology Open Software Suite) is a software analysis package specially developed for the needs of molecular biologists. The software is free Open Source and thus allows other scientists to develop and release new software, integrating also many other available packages and tools for sequence analysis.
Programs
Hundreds of programs (called applications) are collected within EMBOSS, covering different biological areas such as:
- Protein motif identification and domain analysis
- Nucleotide sequence pattern analysis
- Sequence alignment,
- Presentation tools for publication,
and much more.
The EMBOSS applications are organized into groups according to their function (see the Application Groups Documentation for more information).
Some very popular applications are:
- pepstats: Perform several statistics on proteins.
- showfeat: Show features of a sequence.
- patmatmotifs: Compares a protein sequence to the PROSITE motif database.
- abiview: Reads ABI file and display the trace.
- palindrome: looks for inverted repeats in a nucleotide sequence.
- infoseq: Displays some simple information about sequences.
- water: Perform a local alignment of two sequences according to the Smith-Waterman algorithm.
- needle: Perform a global alignment of two sequences according to the Needleman-Wunsch algorithm.
- eprimer3: Picks PCR primers and hybridization oligos on sequences.
- extractseq: Extract regions from a sequence.
- tfscan: Scans DNA sequences for transcription factors.
- tranalign: Align nucleic coding regions given the aligned proteins.
How to reach and use EMBOSS
EMBOSS applications can be searched and launched from the Bioinfo website through the searchable programs interface.
Most of EMBOSS applications can be directly launched by CAPRI.
In the VLS environment, the EMBOSS package is fully available for command line use in the directory /bioprogs/emboss.
References
Rice P, Longden I and Bleasby A EMBOSS: The European Molecular Biology Open Software Suite Trends in Genetics, 2000, 16:276-277.
For more details about EMBOSS, visit the EMBOSS web site