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NEEDLE : Needleman-Wunsch global alignment. (EMBOSS)



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input Section


required Section


advanced Section


output Section


input Section


sequencea -- any [single sequence] (-sequencea) : please enter
either :
  1. the name of a file:
  2. or the actual data here:

(sequence format)


seqall [sequences] (-seqall) : please enter either :

  1. the name of a file:
  2. or the actual data here:

(sequence format)


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required Section

Gap opening penalty (-gapopen)
Gap extension penalty (-gapextend)

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advanced Section


Matrix file (-datafile)

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output Section

Display percent identity and similarity (-similarity)
outfile (-outfile)
Alignment output format (-aformat) ? [default] default fasta MSF

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Some explanations about the options


input Section
enter either the name of a file or the actual data
if you are using Netscape 2.x or later, you can select a file by typing its name, or better, by selecting it with the Netscape file browser (Browse button)
OR you can type your data in the next area, or cut and paste it from another application.
(but not both)

required Section
Gap opening penalty (-gapopen)
The gap open penalty is the score taken away when a gap is created. The best value depends on the choice of comparison matrix. The default value assumes you are using the EBLOSUM62 matrix for protein sequences, and the EDNAFULL matrix for nucleotide sequences. Allowed values: Floating point number from 1.0 to 100.0
Gap extension penalty (-gapextend)
The gap extension, penalty is added to the standard gap penalty for each base or residue in the gap. This is how long gaps are penalized. Usually you will expect a few long gaps rather than many short gaps, so the gap extension penalty should be lower than the gap penalty. An exception is where one or both sequences are single reads with possible sequencing errors in which case you would expect many single base gaps. You can get this result by setting the gap open penalty to zero (or very low) and using the gap extension penalty to control gap scoring. Allowed values: Floating point number from 0.0 to 10.0

output Section
Display percent identity and similarity (-similarity)
Display percent identity and similarity
Sequence format
The sequence will be automatically converted in the format needed for the program
providing you enter a sequence either:
in plain (raw) sequence format or in one of the following known formats:
IG,GenBank,NBRF,EMBL,GCG,DNAStrider,Fitch,fasta,Phylip,PIR,MSF,ASN,PAUP,CLUSTALW
You may enter in the text area a database entry code, or an accession number, in this form:
database:entry_name
or:
database:accession.

Pise form generator version: 5.a (16 Dec 2002 11:54)