| Program name | Author(s) |
Description
|
| aaindexextract | RFCGR |
Extract data from AAINDEX
|
| abiview | RFCGR |
Reads ABI file and display the trace
|
| acdc | Sanger |
Tests definition files for any EMBOSS application.
|
| antigenic | RFCGR |
Finds antigenic sites in proteins
|
| backtranseq | RFCGR |
Back translate a protein sequence
|
| banana | Sanger |
Bending and Curvature Plot in B-DNA
|
| biosed | RFCGR |
Replace or delete sequence sections
|
| btwisted | RFCGR |
Calculates the twisting in a B-DNA sequence
|
| cai | RFCGR |
CAI codon usage statistic
|
| chaos | Sanger |
Create a chaos plot for a sequence.
|
| charge | RFCGR |
Protein charge plot
|
| checktrans | EBI |
ORF property statistics
|
| chips | RFCGR |
Codon usage statistics
|
| cirdna | Norway |
Draws circular maps of DNA constructs
|
| codcmp | RFCGR |
Codon usage table comparison
|
| coderet | RFCGR |
Extract CDS, mRNA and translations from feature tables
|
| compseq | RFCGR |
Counts the composition of dimer/trimer/etc words in a sequence
|
| cons | RFCGR |
Creates a consensus from multiple alignments
|
| cpgplot | RFCGR |
Plot CpG rich areas
|
| cpgreport | RFCGR |
Reports CpG rich regions
|
| cusp | RFCGR |
Create a codon usage table
|
| cutgextract | HGMP |
Extract data from CUTG
|
| cutseq | RFCGR |
Removes a specified section from a sequence.
|
| dan | RFCGR |
Plot melting temperatures for DNA.
|
| dbiblast | Sanger |
Database indexing for BLAST 1 and 2 indexed databases
|
| dbifasta | RFCGR |
Index a fasta database
|
| dbiflat | Sanger |
Database indexing for flat file databases
|
| dbigcg | Sanger |
Database indexing for GCG formatted databases
|
| degapseq | RFCGR |
Removes gap characters from sequences
|
| descseq | RFCGR |
Alter the name or description of a sequence.
|
| diffseq | RFCGR |
Find differences between nearly identical sequences
|
| digest | RFCGR |
Protein proteolytic enzyme or reagent cleavage digest
|
| distmat | RFCGR |
Creates a distance matrix from multiple alignments
|
| dotmatcher | Sanger |
Produces a dotplot of two sequences.
|
| dotpath | RFCGR |
Displays a non-overlapping wordmatch dotplot of two sequences
|
| dottup | Sanger |
DNA sequence dot plot
|
| dreg | Sanger |
Regular expression search of a nucleotide sequence
|
| einverted | Sanger |
Finds DNA inverted repeats
|
| embossdata | RFCGR |
Finds or fetches the data files read in by the EMBOSS programs
|
| embossversion | RFCGR |
Writes the current EMBOSS version number
|
| emowse | RFCGR |
Protein identification by mass spectrometry
|
| emma | RFCGR |
Multiple alignment program
|
| entret | RFCGR |
Reads and writes (returns) flatfile entries
|
| epestfind | Austria |
Finds PEST motifs as potential proteolytic cleavage sites
|
| eprimer3 | RFCGR |
Picks PCR primers and hybridization oligos
|
| equicktandem | Sanger |
Finds tandem repeats
|
| est2genome | Sanger |
Align EST and genomic DNA sequences
|
| etandem | Sanger |
Looks for tandem repeats in a nucleotide sequence.
|
| extractfeat | RFCGR |
Extract features from a sequence
|
| extractseq | RFCGR |
Extract regions from a sequence.
|
| findkm | RFCGR |
Calculates Km and Vmax for an enzyme reaction
|
| freak | RFCGR |
Residue/base frequency table or plot
|
| fuzznuc | RFCGR |
Nucleic acid pattern search
|
| fuzzpro | RFCGR |
Protein pattern search
|
| fuzztran | RFCGR |
Protein pattern search after translation
|
| garnier | EBI |
Predicts protein secondary structure
|
| geecee | Sanger |
Calculates the fractional GC content of nucleic acid sequences
|
| getorf | RFCGR |
Finds and extracts open reading frames (ORFs)
|
| helixturnhelix | RFCGR |
Finds nucleic acid binding domains.
|
| hmoment | RFCGR |
Hydrophobic moment calculation
|
| iep | RFCGR |
Calculates the isoelectric point of a protein
|
| infoalign | RFCGR |
Information on a multiple sequence alignment
|
| infoseq | RFCGR |
Displays some simple information about sequences
|
| isochore | Sanger |
Plots isochores in large DNA sequences
|
| jembossctl | RFCGR |
Jemboss Authentication Control
|
| lindna | Norway |
Draws linear maps of DNA constructs
|
| listor | RFCGR |
Writes a list file of the logical OR of two sets of sequences
|
| marscan | RFCGR |
Finds MAR/SAR sites in nucleic sequences
|
| maskfeat | RFCGR |
Mask off features of a sequence
|
| maskseq | RFCGR |
Mask off regions of a sequence.
|
| matcher | Sanger |
Local alignment of two sequences
|
| megamerger | RFCGR |
Merge two large overlapping nucleic acid sequences
|
| merger | RFCGR |
Merge two overlapping sequences
|
| msbar | RFCGR |
Mutate sequence beyond all recognition
|
| mwcontam | RFCGR |
Shows molwts that match across a set of files
|
| mwfilter | RFCGR |
Filter noisy molwts from mass spec output
|
| needle | RFCGR |
Needleman-Wunsch global alignment.
|
| newcpgreport | EBI |
Report CpG rich areas
|
| newcpgseek | EBI |
Reports CpG rich regions
|
| newseq | RFCGR |
Type in a short new sequence.
|
| noreturn | RFCGR |
Removes carriage return from ASCII files
|
| notseq | RFCGR |
Excludes a set of sequences and writes out the remaining ones
|
| nthseq | RFCGR |
Writes one sequence from a multiple set of sequences
|
| octanol | Sanger |
Displays protein hydropathy
|
| oddcomp | Norway |
Finds protein sequence regions with a biased composition.
|
| palindrome | RFCGR |
Looks for inverted repeats in a nucleotide sequence.
|
| pasteseq | RFCGR |
Insert one sequence into another.
|
| patmatdb | RFCGR |
Matching a Prosite motif against a Protein Sequence Database.
|
| patmatmotifs | RFCGR |
Compares a protein sequence to the PROSITE motif database.
|
| pepcoil | RFCGR |
Predicts coiled coil regions
|
| pepinfo | RFCGR |
Plots simple amino acid properties in parallel
|
| pepnet | RFCGR |
Protein helical net plot
|
| pepstats | RFCGR |
Protein statistics
|
| pepwheel | RFCGR |
Shows protein sequences as helices
|
| pepwindow | Sanger |
Displays protein hydropathy
|
| pepwindowall | Sanger |
Displays protein hydropathy of a set of sequences
|
| plotcon | RFCGR |
Plots the quality of conservation of a sequence alignment
|
| plotorf | RFCGR |
Plot potential open reading frames
|
| polydot | Sanger |
Multiple dotplot
|
| preg | Sanger |
Regular expression search of a protein sequence
|
| prettyplot | Sanger |
Displays aligned sequences, with colouring and boxing.
|
| prettyseq | RFCGR |
Output sequence with translated ranges
|
| primersearch | RFCGR |
Searches DNA sequences for matches with primer pairs
|
| printsextract | RFCGR |
Preprocesses the PRINTS database for use with the program PSCAN
|
| profit | RFCGR |
Scan a sequence or database with a matrix or profile
|
| prophecy | RFCGR |
Creates matrices/profiles from multiple alignments
|
| prophet | RFCGR |
Gapped alignment for profiles
|
| prosextract | RFCGR |
Extracts ID, AC, and PA lines from the PROSITE motif database.
|
| pscan | RFCGR |
Locates fingerprints (multiple motif features) in a protein sequence.
|
| rebaseextract | RFCGR |
Extract data from REBASE
|
| recoder | RFCGR |
Find and remove restriction sites but maintain the same translation
|
| redata | RFCGR |
Isoschizomers, references and Suppliers for Restriction Enzymes
|
| remap | RFCGR |
Display a sequence with restriction cut sites, translation etc..
|
| restover | Sloan-Kettering Cancer Center |
Finds restriction enzymes that produce a specific overhang
|
| restrict | RFCGR |
Finds Restriction Enzyme Cleavage Sites
|
| revseq | RFCGR |
Reverse and complement a sequence.
|
| seealso | RFCGR |
Finds programs sharing group names
|
| seqmatchall | Sanger |
Does an all-against-all comparison of a set of sequences
|
| seqret | Sanger |
Reads and writes (returns) a sequence.
|
| seqretsplit | RFCGR |
Reads and writes (returns) sequences in individual files
|
| showdb | RFCGR |
Displays information on the currently available databases
|
| showalign | RFCGR |
Display a multiple sequence alignment
|
| showfeat | RFCGR |
Show features of a sequence.
|
| showorf | RFCGR |
Pretty output of DNA translations
|
| showseq | RFCGR |
Display a sequence with features, translation etc
|
| shuffleseq | RFCGR |
Shuffles a set of sequences maintaining composition
|
| sigcleave | RFCGR |
Predicts signal peptide cleavage sites
|
| silent | RFCGR |
Silent mutation restriction enzyme scan
|
| sirna | RFCGR |
Finds siRNA duplexes in mRNA
|
| sixpack | LION |
Display a DNA sequence with 6-frame translation and ORFs
|
| skipseq | RFCGR |
Reads and writes (returns) sequences, skipping the first few
|
| splitter | RFCGR |
Split a sequence into (overlapping) smaller sequences.
|
| stretcher | Sanger |
Global alignment of two sequences.
|
| stssearch | Sanger |
Searches a DNA database for matches with a set of STS primers
|
| supermatcher | Sanger |
Finds a match of a large sequence against one or more sequences
|
| syco | RFCGR |
Synonymous codon usage Gribskov statistic plot
|
| tcode | RFCGR |
Fickett TESTCODE statistic to identify protein-coding DNA
|
| textsearch | RFCGR |
Search sequence documentation text. SRS and Entrez are faster!
|
| tfextract | RFCGR |
Extract data from TRANSFAC
|
| tfm | RFCGR |
Displays a program's help documentation manual
|
| tfscan | RFCGR |
Scans DNA sequences for transcription factors.
|
| tmap | Sanger |
Predict transmembrane proteins
|
| tranalign | RFCGR |
Align nucleic coding regions given the aligned proteins
|
| transeq | RFCGR |
Translates nucleic acid sequences.
|
| trimest | RFCGR |
Trim poly-A tails off EST sequences
|
| trimseq | RFCGR |
Trim ambiguous bits off the ends of sequences
|
| twofeat | RFCGR |
Finds neighbouring pairs of features in sequences
|
| union | LION |
Reads sequence fragments and builds one sequence
|
| vectorstrip | RFCGR |
Strips out DNA between a pair of vector sequences
|
| water | RFCGR |
Smith-Waterman local alignment.
|
| whichdb | RFCGR |
Search all databases for an entry
|
| wobble | RFCGR |
Wobble base plot
|
| wordcount | Sanger |
Counts words of a specified size in a DNA sequence.
|
| wordmatch | Sanger |
Finds all exact matches of a given size between 2 sequences
|
| wossname | RFCGR |
Finds programs by keywords in their one-line documentation.
|
| yank | LION |
Reads a range from a sequence, appends the full USA to a list file
|
This allows the EMBOSS libraries to link to other software, and only
requires that software to have an LGPL-compatible licence. Phylip, for
example, fits this model.