|
|
The Applications (programs) |
| 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.
But, to the user they do look exactly like EMBOSS aplications.
| Program name | Author(s) | Description |
|---|---|---|
| eclique | Sanger | Conversion of PHYLIP's clique |
| econsense | Sanger | Conversion of PHYLIP's consense |
| econtml | Sanger | Conversion of PHYLIP's contml |
| econtrast | Sanger | Conversion of PHYLIP's contrast |
| ednacomp | Sanger | Conversion of PHYLIP's dnacomp |
| ednadist | Sanger | Conversion of PHYLIP's dnadist |
| ednainvar | Sanger | Conversion of PHYLIP's dnainvar |
| ednaml | Sanger | Conversion of PHYLIP's dnaml |
| ednamlk | Sanger | Conversion of PHYLIP's dnamlk |
| ednapars | Sanger | Conversion of PHYLIP's dnapars |
| ednapenny | Sanger | Conversion of PHYLIP's dnapenny |
| edollop | Sanger | Conversion of PHYLIP's dollop |
| edolpenny | Sanger | Conversion of PHYLIP's dolpenny |
| efactor | Sanger | Conversion of PHYLIP's factor |
| efitch | Sanger | Conversion of PHYLIP's fitch |
| egendist | Sanger | Conversion of PHYLIP's gendist |
| ekitsch | Sanger | Conversion of PHYLIP's kitsch |
| emix | Sanger | Conversion of PHYLIP's mix |
| eneighbor | Sanger | Conversion of PHYLIP's neighbor |
| epenny | Sanger | Conversion of PHYLIP's penny |
| eprotdist | Sanger | Conversion of PHYLIP's protdist |
| eprotpars | Sanger | Conversion of PHYLIP's protpars |
| erestml | Sanger | Conversion of PHYLIP's restml |
| eseqboot | Sanger | Conversion of PHYLIP's seqboot |
| Program name | Author(s) | Description |
|---|---|---|
| pdbparse | RFCGR | Parses PDB files and writes CCF files (clean coordinate files) for proteins. |
| pdbplus | RFCGR | Add records for residue solvent accessibility and secondary structure to a clean coordinate file. |
| domainer | RFCGR | Reads CCF files (clean coordinate files) for proteins and writes CCF files for domains, taken from a DCF file (domain classification file). |
| scopparse | RFCGR | Reads raw SCOP classification files and writes a DCF file (domain classification file). |
| domainreso | RFCGR | Removes low resolution domains from a DCF file (domain classification file). |
| domainseqs | RFCGR | Adds sequence records to a DCF file (domain classification file). |
| domainnr | RFCGR | Removes redundant domains from a DCF file (domain classification file). The file must contain domain sequence information, which can be added by using DOMAINSEQS. |
| domainrep | RFCGR | Reorder DCF file (domain classification file) so that the representative structure of each user-specified node is given first. |
| domainalign | RFCGR | Generates structure-based sequence alignments for nodes in a DCF file (domain classification file). |
| seqsearch | RFCGR | Generate database hits (sequences) from a DAF file (domain alignment file) or other sequences by using PSI-BLAST. |
| seqfraggle | RFCGR | Removes fragments from DHF files (domain hits files) or other files of sequences. |
| seqsort | RFCGR | Reads DHF files (domain hits files) of database hits (sequences) and removes hits of ambiguous classification. |
| seqnr | RFCGR | Removes redundancy from DHF files (domain hits files) or other files of sequences. |
| seqalign | RFCGR | Reads a DAF file (domain alignment file) and a DHF (domain hits file) and writes a DAF file extended with the hits. |
| siggen | RFCGR | Generates a sparse protein signature from an alignment and residue contact data. |
| libgen | RFCGR | Generates various type of discriminator for each alignment in a directory. |
| libscan | RFCGR | Generates hits (sequences in a domain hits file) from searches of various types of discriminator (HMMs, profiles etc) against a sequence database. Or generates hits from screening sequences against a library of such discriminators. |
| rocon | RFCGR | Reads a DHF file (domain hits file) of hits (sequences of unknown structural classification) and a DHF file of validation sequences (known classification) and writes a "hits file" for the hits, which are classified and rank-ordered on the basis of score. |
| rocplot | RFCGR | A generic and flexible tool for interpretation and graphical display of the performance of predictive methods using receiver Operator Characteristic (ROC) analysis. |
| contacts | RFCGR | Reads CCF files (clean coordinate files) and writes CON files (contact files) of intra-chain residue-residue contact data. |
| interface | RFCGR | Reads protein CCF files (clean coordinate files) and writes CON files (contact files) of inter-chain residue-residue contact data. |
| sites | RFCGR | Reads CCF files (clean coordinate files) and writes CON files (contact files) of residue-ligand contact data for domains in a DCF file (domain classification file). |
| hetparse | RFCGR | Converts raw dictionary of heterogen groups to a file in EMBL-like format. |
| pdbtosp | RFCGR | Convert raw swissprot:PDB equivalence file to EMBL-like format. |
| cathparse | RFCGR | Reads raw CATH classification files and writes DCF file (domain classification file). |
| Program name | Author(s) | Description |
|---|---|---|
| emnu | RFCGR | Simple menu of EMBOSS applications |
| mse | Sanger | Conversion of Will Gilbert's MSE editor |
| topo | Sanger | Conversion of Susan Jean Johns' TOPO |