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hmmsearch(1) |
HMMER Manual |
hmmsearch(1) |
hmmsearch - search profile(s) against a sequence database
hmmsearch [options] hmmfile seqdb
hmmsearch is used to search one or more profiles against a sequence
database. For each profile in hmmfile, use that query profile to search
the target database of sequences in seqdb, and output ranked lists of
the sequences with the most significant matches to the profile. To build
profiles from multiple alignments, see hmmbuild.
Either the query hmmfile or the target seqdb may be
'-' (a dash character), in which case the query profile or target database
input will be read from a stdin pipe instead of from a file. Only one input
source can come through stdin, not both. An exception is that if the
hmmfile contains more than one profile query, then seqdb
cannot come from stdin, because we can't rewind the streaming target
database to search it with another profile.
The output format is designed to be human-readable, but is often
so voluminous that reading it is impractical, and parsing it is a pain. The
--tblout and --domtblout options save output in simple tabular
formats that are concise and easier to parse. The -o option allows
redirecting the main output, including throwing it away in /dev/null.
- -h
- Help; print a brief reminder of command line usage and all available
options.
- -o <f>
- Direct the main human-readable output to a file <f> instead
of the default stdout.
- -A <f>
- Save a multiple alignment of all significant hits (those satisfying
inclusion thresholds) to the file <f>.
- --tblout <f>
- Save a simple tabular (space-delimited) file summarizing the per-target
output, with one data line per homologous target sequence found.
- --domtblout <f>
- Save a simple tabular (space-delimited) file summarizing the per-domain
output, with one data line per homologous domain detected in a query
sequence for each homologous model.
- --acc
- Use accessions instead of names in the main output, where available for
profiles and/or sequences.
- --noali
- Omit the alignment section from the main output. This can greatly reduce
the output volume.
- --notextw
- Unlimit the length of each line in the main output. The default is a limit
of 120 characters per line, which helps in displaying the output cleanly
on terminals and in editors, but can truncate target profile description
lines.
- --textw <n>
- Set the main output's line length limit to <n> characters per
line. The default is 120.
Reporting thresholds control which hits are reported in output files (the main
output, --tblout, and --domtblout). Sequence hits and domain
hits are ranked by statistical significance (E-value) and output is generated
in two sections called per-target and per-domain output. In per-target output,
by default, all sequence hits with an E-value <= 10 are reported. In the
per-domain output, for each target that has passed per-target reporting
thresholds, all domains satisfying per-domain reporting thresholds are
reported. By default, these are domains with conditional E-values of <= 10.
The following options allow you to change the default E-value reporting
thresholds, or to use bit score thresholds instead.
- -E <x>
- In the per-target output, report target sequences with an E-value of <=
<x>. The default is 10.0, meaning that on average, about 10
false positives will be reported per query, so you can see the top of the
noise and decide for yourself if it's really noise.
- -T <x>
- Instead of thresholding per-profile output on E-value, instead report
target sequences with a bit score of >= <x>.
- --domE <x>
- In the per-domain output, for target sequences that have already satisfied
the per-profile reporting threshold, report individual domains with a
conditional E-value of <= <x>. The default is 10.0. A
conditional E-value means the expected number of additional false positive
domains in the smaller search space of those comparisons that already
satisfied the per-target reporting threshold (and thus must have at least
one homologous domain already).
- --domT <x>
- Instead of thresholding per-domain output on E-value, instead report
domains with a bit score of >= <x>.
Inclusion thresholds are stricter than reporting thresholds. Inclusion
thresholds control which hits are considered to be reliable enough to be
included in an output alignment or a subsequent search round, or marked as
significant ("!") as opposed to questionable ("?") in
domain output.
- --incE <x>
- Use an E-value of <= <x> as the per-target inclusion
threshold. The default is 0.01, meaning that on average, about 1 false
positive would be expected in every 100 searches with different query
sequences.
- --incT <x>
- Instead of using E-values for setting the inclusion threshold, instead use
a bit score of >= <x> as the per-target inclusion
threshold. By default this option is unset.
- --incdomE <x>
- Use a conditional E-value of <= <x> as the per-domain
inclusion threshold, in targets that have already satisfied the overall
per-target inclusion threshold. The default is 0.01.
- --incdomT <x>
- Instead of using E-values, use a bit score of >= <x> as
the per-domain inclusion threshold.
Curated profile databases may define specific bit score thresholds for each
profile, superseding any thresholding based on statistical significance alone.
To use these options, the profile must contain the appropriate
(GA, TC, and/or NC) optional score threshold annotation; this is picked up
by hmmbuild from Stockholm format alignment files. Each thresholding
option has two scores: the per-sequence threshold <x1> and the
per-domain threshold <x2> These act as if -T <x1>
--incT <x1> --domT <x2>
--incdomT <x2> has been applied specifically using each
model's curated thresholds.
- --cut_ga
- Use the GA (gathering) bit scores in the model to set per-sequence (GA1)
and per-domain (GA2) reporting and inclusion thresholds. GA thresholds are
generally considered to be the reliable curated thresholds defining family
membership; for example, in Pfam, these thresholds define what gets
included in Pfam Full alignments based on searches with Pfam Seed models.
- --cut_nc
- Use the NC (noise cutoff) bit score thresholds in the model to set
per-sequence (NC1) and per-domain (NC2) reporting and inclusion
thresholds. NC thresholds are generally considered to be the score of the
highest-scoring known false positive.
- --cut_tc
- Use the TC (trusted cutoff) bit score thresholds in the model to set
per-sequence (TC1) and per-domain (TC2) reporting and inclusion
thresholds. TC thresholds are generally considered to be the score of the
lowest-scoring known true positive that is above all known false
positives.
HMMER3 searches are accelerated in a three-step filter pipeline: the MSV filter,
the Viterbi filter, and the Forward filter. The first filter is the fastest
and most approximate; the last is the full Forward scoring algorithm. There is
also a bias filter step between MSV and Viterbi. Targets that pass all the
steps in the acceleration pipeline are then subjected to postprocessing --
domain identification and scoring using the Forward/Backward algorithm.
Changing filter thresholds only removes or includes targets from
consideration; changing filter thresholds does not alter bit scores,
E-values, or alignments, all of which are determined solely in
postprocessing.
- --max
- Turn off all filters, including the bias filter, and run full
Forward/Backward postprocessing on every target. This increases
sensitivity somewhat, at a large cost in speed.
- --F1 <x>
- Set the P-value threshold for the MSV filter step. The default is 0.02,
meaning that roughly 2% of the highest scoring nonhomologous targets are
expected to pass the filter.
- --F2 <x>
- Set the P-value threshold for the Viterbi filter step. The default is
0.001.
- --F3 <x>
- Set the P-value threshold for the Forward filter step. The default is
1e-5.
- --nobias
- Turn off the bias filter. This increases sensitivity somewhat, but can
come at a high cost in speed, especially if the query has biased residue
composition (such as a repetitive sequence region, or if it is a membrane
protein with large regions of hydrophobicity). Without the bias filter,
too many sequences may pass the filter with biased queries, leading to
slower than expected performance as the computationally intensive
Forward/Backward algorithms shoulder an abnormally heavy load.
- --nonull2
- Turn off the null2 score corrections for biased composition.
- -Z <x>
- Assert that the total number of targets in your searches is
<x>, for the purposes of per-sequence E-value calculations,
rather than the actual number of targets seen.
- --domZ <x>
- Assert that the total number of targets in your searches is
<x>, for the purposes of per-domain conditional E-value
calculations, rather than the number of targets that passed the reporting
thresholds.
- --seed <n>
- Set the random number seed to <n>. Some steps in
postprocessing require Monte Carlo simulation. The default is to use a
fixed seed (42), so that results are exactly reproducible. Any other
positive integer will give different (but also reproducible) results. A
choice of 0 uses a randomly chosen seed.
- --tformat <s>
- Assert that target sequence file seqfile is in format
<s>, bypassing format autodetection. Common choices for
<s> include: fasta, embl, genbank.
Alignment formats also work; common choices include: stockholm,
a2m, afa, psiblast, clustal, phylip.
For more information, and for codes for some less common formats, see main
documentation. The string <s> is case-insensitive
(fasta or FASTA both work).
- --cpu <n>
- Set the number of parallel worker threads to <n>. On
multicore machines, the default is 2. You can also control this number by
setting an environment variable, HMMER_NCPU. There is also a master
thread, so the actual number of threads that HMMER spawns is
<n>+1.
This option is not available if HMMER was compiled with POSIX
threads support turned off.
- --stall
- For debugging the MPI master/worker version: pause after start, to enable
the developer to attach debuggers to the running master and worker(s)
processes. Send SIGCONT signal to release the pause. (Under gdb: (gdb)
signal SIGCONT) (Only available if optional MPI support was enabled at
compile-time.)
- --mpi
- Run under MPI control with master/worker parallelization (using
mpirun, for example, or equivalent). Only available if optional MPI
support was enabled at compile-time.
See hmmer(1) for a master man page with a list of all the individual man
pages for programs in the HMMER package.
For complete documentation, see the user guide that came with your
HMMER distribution (Userguide.pdf); or see the HMMER web page
(http://hmmer.org/).
Copyright (C) 2019 Howard Hughes Medical Institute.
Freely distributed under the BSD open source license.
For additional information on copyright and licensing, see the
file called COPYRIGHT in your HMMER source distribution, or see the HMMER
web page (http://hmmer.org/).
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