![]() |
The Software List |
| Program name | Source | Description |
|---|---|---|
| A | next | Back Top |
| aacomp | FastA | Calculates the amino acid composition and molecular weight of a sequence. |
| acdc | EMBOSS | Tests definition files for any EMBOSS application. |
| align | FastA | Optimal global alignment of two sequences |
| align0 | FastA | As align, but does not penalize for end-gaps. |
| antigenic | EMBOSS | Finds antigenic sites in proteins |
| Assemble | GCG | Combines fragments into one sequence |
| B | next | Back Top |
| backtranseq | EMBOSS | Back translate a protein sequence |
| BackTranslate | GCG | Back translate a protein sequence |
| banana | EMBOSS | Bending and Curvature Plot in B-DNA |
| BestFit | GCG | Smith-Waterman local alignments |
| bestscor | FastA | Calculates the best self-comparison score. |
| BLAST | GCG | Blast on local databases |
| Breakup | GCG | Breaks large files into smaller overlapping ones |
| C | next | Back Top |
| chaos | EMBOSS | Create a chaos plot for a sequence. |
| checktrans | EMBOSS | ORF property statistics |
| chips | EMBOSS | Codon usage statistics |
| Chopup | GCG | Converts very long lines in files to small ones |
| cirdna | EMBOSS | Draws circular maps of DNA constructs |
| clique | Phylip | Finds largest clique of mutually compatible characters. |
| clustalw | igmbc-fr | Multiple alignment program (command line based). |
| clustalx | igmbc-fr | Multiple alignment program (X-windows based). |
| cluster | EMBOSS | DNA sequence clustering |
| codcmp | EMBOSS | Codon usage table comparison |
| CodonFrequency | GCG | Tabulates the codon frequency in sequences |
| CodonPreference | GCG | Gene finder based on codon frequency |
| CoilScan | GCG | Finds coiled coil segments in proteins |
| Compare | GCG | Compares two sequences to make a file for DotPlot |
| complex | EMBOSS | Find the linguistic complexity in nucleotide sequences |
| Composition | GCG | Determines the nucleic/amino acid composition of sequences |
| CompressText | GCG | Removes "white space" from files |
| compseq | EMBOSS | Counts the composition of dimer/trimer/etc words in a sequence |
| CompTable | GCG | Create a (simplified) scoring matrix. |
| consense | Phylip | Computes majority-rule and strict consensus trees. |
| Consensus | GCG | Generates a consensus sequence for short nucleotide sequences. |
| contml | Phylip | Phylogenies from maximum likelihood on gene frequency data. |
| contrast | Phylip | Computes contrasts and correlations for comparative method studies. |
| Correspond | GCG | Compares patterns of codon usage. |
| Corrupt | GCG | Randomly introduce mutations into a nucleotide sequence. |
| cpgplot | EMBOSS | Plot CpG rich areas |
| cpgreport | EMBOSS | Reports CpG rich regions |
| crandseq | FastA | Produces a randomly shuffled DNA sequence keeping the codons intact. |
| cusp | EMBOSS | Create a codon usage table |
| cutseq | EMBOSS | Removes a specified section from a sequence. |
| D | next | Back Top |
| dan | EMBOSS | Plot melting temperatures for DNA. |
| DataSet | GCG | Creates a GCG data library from GCG sequences |
| dbiblast | EMBOSS | Database indexing for BLAST 1 and 2 indexed databases |
| dbifasta | EMBOSS | Index a fasta database |
| dbiflat | EMBOSS | Database indexing for flat file databases |
| dbigcg | EMBOSS | Database indexing for GCG formatted databases |
| descseq | EMBOSS | Alter the name or description of a sequence. |
| Detab | GCG | Replaces tab characters with spaces. |
| diffseq | EMBOSS | Find differences (SNPs) between nearly identical sequences |
| digest | EMBOSS | Protein proteolytic enzyme or reagent cleavage digest |
| Distances | GCG | Creates a table of pair-wise distances from aligned sequences. |
| Diverge | GCG | Estimate the number of substitutions between two coding sequences. |
| dnacomp | Phylip | Phylogenies from DNA by the Compatibility criterion. |
| dnadist | Phylip | Computes four distance measures from nucleic acid sequences. |
| dnainvar | Phylip | Phylogenetic invariants method. |
| dnaml | Phylip | Phylogenies from DNA by maximum likelihood. |
| dnamlk | Phylip | Phylogenies from DNA by maximum likelihood with a molecular clock. |
| dnamove | Phylip | Interactive DNA phylogenies by parsimony or compatibility. |
| dnapars | Phylip | Nucleotide phylogenies by parsimony methods. |
| dnapenny | Phylip | DNA phylogenies by branch-and-bound. |
| dollop | Phylip | Phylogenies from the Dollo or polymorphism parsimony criteria. |
| dolmove | Phylip | Interactive construction of phylogenies using the Dollo or polymorphism parsimony criteria. |
| dolpenny | Phylip | Branch-and-bound phylogenies from the Dollo or polymorphism parsimony criteria. |
| dotmatcher | EMBOSS | Produces a dotplot of two sequences. |
| dotpath | EMBOSS | Displays a non-overlapping wordmatch dotplot of two sequences |
| DotPlot | GCG | Creates a dot plot using a file from Compare or StemLoop. |
| dottup | EMBOSS | DNA sequence dot plot |
| drawgram | Phylip | Draws cladograms and phenograms. |
| drawtree | Phylip | Draws unrooted phylogenies. |
| dreg | EMBOSS | Regular expression search of a nucleotide sequence |
| E | next | Back Top |
| einverted | EMBOSS | Finds DNA inverted repeats |
| embossdata | EMBOSS | Finds or fetches the data files read in by the EMBOSS programs |
| emma | EMBOSS | Multiple alignment program |
| equicktandem | EMBOSS | Finds tandem repeats |
| est2genome | EMBOSS | Align EST and genomic DNA sequences |
| etandem | EMBOSS | Looks for tandem repeats in a nucleotide sequence. |
| extractseq | EMBOSS | Extract regions from a sequence. |
| ExtractPeptide | GCG | Writes a peptide sequence from a frame of Map. |
| F | next | Back Top |
| factor | Phylip | Recodes multistate data to two state data. |
| FastA | GCG | FastA on local databases. |
| FastX | GCG | FastX on local databases. |
| Fetch | GCG | Get a sequence from a GCG database. |
| Figure | GCG | Makes figures from GCG program output. |
| findkm | EMBOSS | Calculates Km and Vmax for an enzyme reaction |
| FindPatterns | GCG | Searches for short patterns in sequences. |
| FingerPrint | GCG | Identifies products of T1 ribonuclease digestion. |
| fitch | Phylip | Phylogenies by the Fitch-Margoliash and least-squares methods. |
| FitConsensus | GCG | Finds matches to a consensus sequence matrix. |
| flalign | FastA | Plots lalign local alignments to a GCG Figure file. |
| FrameAlign | GCG | Local (or Global) alignment of a protein sequence to all frames of a nucleic acid sequence. |
| Frames | GCG | Translates in all six frames. |
| FrameSearch | GCG | Aligns groups of protein sequences to nucleotide sequence(s) in all frames. |
| freak | EMBOSS | Residue/base frequency table or plot |
| FromEMBL | GCG | Reformats an EMBL distribution file to GCG format. |
| FromFastA | GCG | Reformats FastA format files to GCG format. |
| fromgb | FastA | Convert from GenBank LOCUS format to Pearson/FASTA format. |
| FromGenBank | GCG | Reformats GenBank distribution files to GCG format. |
| FromIG | GCG | Reformats IntelliGenetics files to GCG format. |
| FromPIR | GCG | Reformat PIR format files to GCG format. |
| FromStaden | GCG | Reformat Staden format files to GCG format. |
| fuzznuc | EMBOSS | Nucleic acid pattern search |
| fuzzpro | EMBOSS | Protein pattern search |
| fuzztran | EMBOSS | Protein pattern search after translation |
| G | next | Back Top |
| Gap | GCG | Needleman-Wunsch global alignment |
| gap4 | Staden | Performs assembly, contig joining, assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. |
| Gapshow | GCG | Graphical representation of an alignment. |
| garnier | EMBOSS | Predicts protein secondary structure |
| garnier | FastA | Secondary structure prediction by the GOR method. |
| GCGtoBLAST | GCG | Combines GCG format sequences into a Blast searchable database. |
| geecee | EMBOSS | Calculates the fractional GC content of a nucleic acid sequence |
| GelAssemble | GCG | Multiple sequence editor for assembled contigs. |
| GelDisassemble | GCG | Breaks up contigs into single fragments. |
| GelEnter | GCG | Adds fragments to an assembly project. |
| GelMerge | GCG | Aligns sequence assembly fragments into contigs |
| GelStart | GCG | Starts a new fragment assembly project. |
| GelView | GCG | Displays structure of contigs in an assembly project. |
| gendist | Phylip | Computes three genetic distances from gene frequency data. |
| getorf | EMBOSS | Finds and extracts open reading frames (ORFs) |
| GetSeq | GCG | Create a sequence file from a terminal. |
| grease | FastA | Kyte-Doolittle hydropathicity profile |
| GrowTree | GCG | Generates a tree from a distance matrix. |
| H | next | Back Top |
| HelicalWheel | GCG | Plots a peptide sequence as a helical wheel. |
| helixturnhelix | EMBOSS | Finds nucleic acid binding domains. |
| HTHScan | GCG | Searches for helix-turn-helix motifs. |
| I | next | Back Top |
| iep | EMBOSS | Calculates the isoelectric point of a protein |
| infoseq | EMBOSS | Displays some simple information about sequences |
| isochore | EMBOSS | Plots isochores in large DNA sequences |
| Isoelectric | GCG | Plots charge as a function of pH for a peptide sequence. |
| J | next | Back Top |
| K | next | Back Top |
| kitsch | Phylip | Phylogenies by the Fitch-Margoliash and least-squares methods with a molecular clock. |
| L | next | Back Top |
| lalign | FastA | Local sequence alignment program that displays the N-best local alignments. |
| lfasta | FastA | local similarity searches showing local alignments. |
| lindna | EMBOSS | Draws linear maps of DNA constructs |
| LineUp | GCG | Editor for multiple alignments. |
| ListFile | GCG | Print a file on a terminals by pass port. |
| LookUp | GCG | Find a sequence data base entry by SRS. |
| LPrint | GCG | Prints a PostScript file. |
| M | next | Back Top |
| Map | GCG | Find restriction enzyme sites. |
| MapPlot | GCG | Displays restriction enzyme sites graphically. |
| MapSort | GCG | Sorts restriction enzyme digest fragments by size. |
| maskseq | EMBOSS | Mask off regions of a sequence. |
| matcher | EMBOSS | Local alignment of two sequences |
| megamerger | EMBOSS | Merge two large overlapping nucleic acid sequences |
| MEME | GCG | Finds conserved motifs in a group of unaligned sequences. |
| merger | EMBOSS | Merge two overlapping sequences |
| MFold | GCG | Predicts optimal secondary structure in nucleotide sequences. |
| mix | Phylip | Wagner, Camin-Sokal and mixed parsimony methods. |
| Moment | GCG | Makes a contour plot of the helical hydrophobic moment of a peptide sequence. |
| Motifs | GCG | Searches for ProSite patterns in a sequence. |
| MotifSearch | GCG | Searches a set of sequences with a profile. |
| move | Phylip | Interactive construction of phylogenies from two-state data. |
| msbar | EMBOSS | Mutate sequence beyond all recognition |
| N | next | Back Top |
| Name | GCG | Change GCG logical names. |
| Names | GCG | Identifies GCG data files and sequence entries by name |
| needle | EMBOSS | Needleman-Wunsch global alignment. |
| neighbor | Phylip | Neighbour-joining and UPGMA methods. |
| NetBLAST | GCG | Blast search at NCBI. |
| NetFetch | GCG | Interface to NetEntrez to get sequences from NetBlast search. |
| newcpgreport | EMBOSS | Report CpG rich areas |
| newcpgseek | EMBOSS | Reports CpG rich regions |
| newseq | EMBOSS | Type in a short new sequence. |
| nip4 | Staden | Analyses nucleotide sequences to find genes, restriction sites and motifs. It will perform translations, find ORFs and examine codon usage. |
| NoOverlap | GCG | Identifies where a group of nucleotide sequences have no common subsequences. |
| noreturn | EMBOSS | Removes carriage return from ASCII files |
| nthseq | EMBOSS | Writes one sequence from a multiple set of sequences |
| O | next | Back Top |
| octanol | EMBOSS | Displays protein hydropathy |
| oddcomp | EMBOSS | Finds protein sequence regions with a biased composition. |
| OldDistances | GCG | Makes a table of pairwise similarities from aligned sequences. |
| OneCase | GCG | Changes the case of the letters in a file. |
| Overlap | GCG | Looks for overlaps in a set of sequences. |
| P | next | Back Top |
| palindrome | EMBOSS | Looks for inverted repeats in a nucleotide sequence. |
| pasteseq | EMBOSS | Insert one sequence into another. |
| patmatdb | EMBOSS | Matching a Prosite motif against a Protein Sequence Database. |
| patmatmotifs | EMBOSS | Compares a protein sequence to the PROSITE motif database. |
| PAUPDisplay | GCG | An interface to tree manipulation, diagnosis, and display options in PAUP |
| PAUPSearch | GCG | An interface to the tree-searching options in PAUP |
| penny | Phylip | Finds all most parsimonious trees by branch-and-bound. |
| pepcoil | EMBOSS | Predicts coiled coil regions |
| PepData | GCG | Translates in six frames and concatenates peptide sequences |
| pepinfo | EMBOSS | Plots simple amino acid properties in parallel |
| pepnet | EMBOSS | Protein helical net plot |
| PepPlot | GCG | Plots measures of protein secondary structure and hydrophobicity |
| pepstats | EMBOSS | Protein statistics such as isoelectric point and molecular weight |
| PeptideMap | GCG | Marks a peptide sequence where a known proteolytic agent might cut it. |
| Peptidesort | GCG | Orders the fragments from a digest of an amino acid sequence. |
| PeptideStructure | GCG | Secondary structure and related predictions for a peptide sequence. |
| pepwheel | EMBOSS | Protein helical wheel plot |
| pepwindow | EMBOSS | Displays protein hydropathy |
| pepwindowall | EMBOSS | Displays protein hydropathy of a set of sequences |
| PileUp | GCG | Multiple sequence alignment from progressive (tree based), pairwise alignments |
| plalign | FastA | Plots lalign local alignments to a postscript file. |
| PlasmidMap | GCG | Draws a circular plot of a plasmid construct. |
| plotorf | EMBOSS | Plot potential open reading frames |
| Plotsimilarity | GCG | Plots a running average of similarity among sequences in a multiple alignment. |
| PlotStructure | GCG | Plots the measures of protein secondary structure from PeptideStructure. |
| PlotTest | GCG | Plots an example graphic to test your graphics configuration. |
| polydot | EMBOSS | Multiple dotplot |
| prdf2 | FastA | Calculates the probability of a similarity score using an extreme value distribution. |
| preg | EMBOSS | Regular expression search of a protein sequence |
| pregap4 | Staden | Prepares sequence trace data for analysis or assembly. |
| Pretty | GCG | Displays multiple sequence alignments and calculates a consensus sequence. |
| PrettyBox | GCG | Displays multiple sequence alignments in PostScript format, using shading. |
| prettyplot | EMBOSS | Displays aligned sequences, with colouring and boxing. |
| prettyseq | EMBOSS | Output sequence with translated ranges |
| prima | EMBOSS | Selecting primers for PCR and DNA amplification. |
| Prime | GCG | Selects oligonucleotide primers for a template DNA sequence. |
| primersearch | EMBOSS | Searches DNA sequences for matches with primer pairs |
| printsextract | EMBOSS | Preprocesses the PRINTS database for use with the program PSCAN |
| ProfileGap | GCG | Makes an optimal alignment between a profile and one or more sequences. |
| ProfileMake | GCG | Creates a position-specific scoring table or profile. |
| ProfileScan | GCG | Finds motifs in a database of profiles. |
| ProfileSearch | GCG | Uses a profile to search a database. |
| ProfileSegments | GCG | Makes optimal alignments from similar segments found by ProfileSearch. |
| profit | EMBOSS | Scan a sequence or database with a matrix or profile |
| prophecy | EMBOSS | Creates matrices/profiles from multiple alignments |
| prophet | EMBOSS | Gapped alignment for profiles |
| prosextract | EMBOSS | Extracts ID, AC, and PA lines from the PROSITE motif database. |
| protdist | Phylip | Compute distance measures from protein sequences. |
| protpars | Phylip | Phylogenies by protein parsimony. |
| prss3 | FastA | Evaluates the significance of pairwise similarity scores using a Monte Carlo analysis. |
| pscan | EMBOSS | Locates fingerprints (multiple motif features) in a protein sequence. |
| Publish | GCG | Arranges sequences for publication. |
| Q | next | Back Top |
| R | next | Back Top |
| randseq | FastA | Produces a randomly shuffled sequence from a query sequence. |
| Readseq | D. Gilbert | General sequence reformatting tool. |
| rebaseextract | EMBOSS | Extract data from REBASE |
| Red | GCG | A text formatter that creates publication-quality documents for a PostScript printer |
| redata | EMBOSS | Isoschizomers, references and Suppliers for Restriction Enzymes |
| Reformat | GCG | Rewrites sequence, scoring matrix, or enzyme data file(s) in GCG format. |
| remap | EMBOSS | Display a sequence with restriction cut sites, translation etc.. |
| Repeat | GCG | Finds direct repeats in sequences. |
| Replace | GCG | Makes character string replacements in text file(s). |
| restml | Phylip | Phylogenies by maximum likelihood from restriction enzyme data. |
| restrict | EMBOSS | Finds Restriction Enzyme Cleavage Sites |
| retree | Phylip | Reroot, flip branches and change species names and branch lengths. |
| Reverse | GCG | Reverses and/or complements a sequence. |
| revseq | EMBOSS | Reverse and complement a sequence. |
| S | next | Back Top |
| Sample | GCG | Extracts sequence fragments randomly from sequence(s). |
| seealso | EMBOSS | Finds programs sharing group names |
| Seg | GCG | Replaces low complexity regions in protein sequences with X characters. |
| Segments | GCG | Aligns and displays the segments of similarity found by WordSearch. |
| seqboot | Phylip | Bootstrap, jack-knife or permutation resampling analyses. |
| SeqEd | GCG | An interactive editor for entering and modifying sequences |
| SeqLab | GCG | The graphical user interface (X-windows) for the GCG Package. |
| seqmatchall | EMBOSS | All against all word based sequence comparison |
| seqret | EMBOSS | Reads and writes (returns) a sequence. |
| seqretall | EMBOSS | Reads and writes (returns) a set of sequences one at a time. |
| seqretset | EMBOSS | Reads and writes (returns) a set of sequences all at once. |
| SetKeys | GCG | Redefines your keyboard's keys for easier sequence entry in GCG programs. |
| SetPlot | GCG | Lists graphic devices available to the GCG programs. |
| ShiftOver | GCG | Moves a file to the right or left a few columns. |
| showdb | EMBOSS | Displays information on the currently available databases |
| showfeat | EMBOSS | Show features of a sequence. |
| showorf | EMBOSS | Pretty output of DNA translations |
| showseq | EMBOSS | Display a sequence with features, translation etc |
| Shuffle | GCG | Randomizes the order of a sequence without changing the composition. |
| shuffleseq | EMBOSS | Shuffles a set of sequences maintaining composition |
| sigcleave | EMBOSS | Predicts signal peptide cleavage sites. |
| Simplify | GCG | Reduces the number of symbols in a sequence based on similar properties. |
| sip4 | Staden | Compares pairs of sequences. It includes dot plots, finding matching words, global and local optimal alignments and statistical evaluation of matches. |
| Spew | GCG | sends a GCG sequence to a personal computer acting as a terminal. |
| splitter | EMBOSS | Split a sequence into (overlapping) smaller sequences. |
| SPScan | GCG | Looks for the presence of secretory signal peptides. |
| SSearch | GCG | Smith-Waterman search of local GCG databases. |
| StatPlot | GCG | Plots a set of graphs from a table of numbers (eg from Window). |
| Stemloop | GCG | Finds stems (inverted repeats) within a sequence. |
| stretcher | EMBOSS | Global alignment of two sequences. |
| StringSearch | GCG | Identifies sequences by character patterns in the sequence documentation. |
| stssearch | EMBOSS | Searches a DNA sequence database with a set of STS primers and reports expected matches and possible mismatches. A replacement for stssearch in the EGCG package. |
| supermatcher | EMBOSS | Finds a match of one sequence against one or more sequences (for Large Sequences) |
| syco | EMBOSS | Synonymous codon usage Gribskov statistic plot |
| Symbol | GCG | Creates, changes, deletes, or displays GCG symbol(s) in the GCG symbol table. |
| T | next | Back Top |
| Terminator | GCG | Searches for prokaryotic factor-independent RNA polymerase terminators. |
| TestCode | GCG | Identify potential protein coding regions by non-random third base composition. |
| textsearch | EMBOSS | Search sequence documentation text. SRS and Entrez are faster! |
| TFastA | GCG | TFasta on local (translated nucleotide) GCG databases. |
| TFastX | GCG | As TFasta but allowing for frame shifts. |
| tfextract | EMBOSS | Extract data from TRANSFAC |
| tfm | EMBOSS | Displays a program's help documentation manual |
| tfscan | EMBOSS | Scans DNA sequences for transcription factors. |
| tgrease | FastA | Graphic plot of Kyte-Doolittle hydropathicity profile. |
| tmap | EMBOSS | Predict transmembrane proteins |
| ToFastA | GCG | Converts GCG sequence(s) into FastA format. |
| ToIG | GCG | Converts GCG sequence file(s) into a single file in IntelliGenetics format. |
| ToPIR | GCG | Writes GCG sequence(s) into a single file in PIR format. |
| ToStaden | GCG | Writes a GCG sequence into a file in Staden format. |
| transeq | EMBOSS | Translates nucleic acid sequences. |
| Translate | GCG | Translates nucleotide sequences into peptide sequences. |
| trev | Staden | Allows viewing and editing of ABI, ALF or SCF trace files. |
| trimseq | EMBOSS | Trim ambiguous bits off the ends of sequences |
| U | next | Back Top |
| V | next | Back Top |
| vectorstrip | EMBOSS | Strips out DNA between a pair of vector sequences |
| W | next | Back Top |
| water | EMBOSS | Smith-Waterman local alignment. |
| Window | GCG | Makes a table of the frequencies of sequence patterns within a window along a sequence. |
| wobble | EMBOSS | Wobble base plot |
| wordcount | EMBOSS | Counts words of a specified size in a DNA sequence. |
| wordmatch | EMBOSS | Finds all exact matches of a given size between 2 DNA sequences |
| WordSearch | GCG | Identifies sequences in a database by matching large numbers of words. |
| wossname | EMBOSS | Finds programs by keywords in their one-line documentation. |
| X | next | Back Top |
| Xnu | GCG | Masks tandem repeats in protein sequences with X characters. |
| Y | next | Back Top |
| Z | next | Back Top |
| zs_exp | FastA | Converts a z-score (mean 50, s.d. 10) into an expectation value using the extreme value distribution and the size of the database |
| Home | Introduction | Software | I Want To... | People |
| Research | Education | Web Resources | Search |
times.