NAME

SYNOPSIS

DESCRIPTION

hmmfs is designed to be particularly useful for detecting repeated motifs in long sequences. It has been used successfully for Alu detection in human cosmid sequences, and for recognizing multiple tandem domains in mosaic proteins.

The memory requirement is linear in the length of the longest database sequence, not quadratic, permitting very long genomic DNA sequences (> 1 Mb) to be searched.

The scores reported by hmmfs are in bits of information. Specifically, they are log-odds scores: the log of the ratio of the probability of the sequence given the model and the probability of the sequence given a simple random sequence model. This score is related to the statistical significance of the alignment. A score of zero is marginal; according to the model's statistics, it's 50% likely that the alignment is a real match to the model, and 50% likely that it's not. The higher the score, the better; a score of 100 means that it is 2^100-fold more likely that the sequence is a match to the model than not. In practice, a database contains many more unrelated sequences than related ones, so the actual score required for statistical significance is somewhat higher than zero -- as a rule of thumb for protein database searches, don't trust scores lower than the log2 of the number of seqs in the database). This is 16 bits for our current SWIR5 composite protein database of 57,000 sequences. See the User Guide for more details.

Note the differences between the different HMM searching programs. hmms looks for a global alignment of HMM to sequences (Needleman/Wunsch style); overhangs of unmatches sequence are not permitted, and the full model must be matched. hmmls looks for one or more local alignments of the full model to a subsequence of each database sequence; unmatches sequence overhangs are allowed. hmmsw looks for the best fragmentary match of a subsequence to part of the model (Smith/Waterman style). hmmfs looks for multiple non-overlapping matches of subsequences to parts of the model (modified multiple-hit Smith/Waterman). hmms is useful for scoring or detecting whole proteins with complete models; hmmls is useful for scoring or detecting intact domains in protein sequences or complete repeats in nucleic acid sequences; hmmsw is useful for general protein database searching, allowing for possible incomplete matches to a model; hmmfs is useful for general nucleic acid database searching or for scoring/detecting domains in multidomain proteins, allowing for multiple non-overlapping matches per sequence.

OPTIONS

-c

Search complementary strand too. DNA/RNA only; undefined behavior on protein sequences or models.

-h

Print short usage and help info for the program.

-q

quiet -- suppress the verbose banner. Useful for piping the output of hmmfs into another program or script.

-r <rfile>

Read the random sequence model from <rfile>. This model is used as the null hypothesis for calculating log-odds alignment scores.

-t <thresh>

Report only matches above a score of <thresh> bits. Only well-defined for thresholds greater than or equal to zero.

-F

For each hit, print a "fancy" BLAST-style representation of the alignment to the model. Three lines are shown; a line for the model consensus, a line for the matched positions, and a line for the sequence. In the model consensus line, upper-case letters represent strong consensus positions, lower-case letters represent the best identity at a weak consensus position. (Strong and weak are arbitrarily defined; for protein models, log-odds symbol scores above 2.0 bits are called "strong" consensus.) On the match line, letters represent exact matches to the highest scoring possible residue according to the HMM, and +'s represent matches to positive-scoring residues.

Individual man pages: hmma(l), hmmb(l), hmme(l), hmmls(l), hmms(l), hmmsw(l), hmmt(l), hmm-convert(l)

User guide and tutorial: Userguide.ps

BUGS

Not very tolerant of errors on the command line.

NOTES

Sean Eddy
Dept. of Genetics, Washington Univ. School of Medicine 660 S. Euclid Box 8232
St Louis, MO 63110 USA
Phone: 1-314-362-7666
FAX : 1-314-362-2985
Email: eddy@genetics.wustl.edu

Table of Contents

• NAME
• SYNOPSIS
• DESCRIPTION
• OPTIONS
• SEE ALSO
• BUGS
• NOTES