vsearch

Versatile open-source tool for microbiome analysis

View on GitHub

NAME

vsearch \-\-search_exact — search for exact full-length matches against a database

SYNOPSIS

vsearch \-\-search_exact fastxfile \-\-db filename (\-\-alnout | \-\-biomout | \-\-blast6out | \-\-fastapairs | \-\-matched | \-\-mothur_shared_out | \-\-notmatched | \-\-otutabout | \-\-samout | \-\-uc | \-\-userout) filename [options]

DESCRIPTION

The vsearch command --search_exact searches the query sequences in a fasta or fastq file against a database of target sequences (--db), reporting only 100% exact full-length matches. It is much faster than --usearch_global for this use case.

Because only exact matches are reported, --id, --maxaccepts, and --maxrejects do not apply and are not accepted. Masking is controlled with --qmask (queries) and --dbmask (database). By default only the plus strand is searched; use --strand both to also check the reverse complement.

At least one output option must be specified. This command is multi-threaded.

The --qsegout and --tsegout options do not count as sole output options: when either is used on its own, vsearch rejects the run with “No output files specified”. They can still be used, but only in combination with one of the output options listed in the SYNOPSIS.

OPTIONS

mandatory options

--db must be specified, along with at least one output option.

--db filename
Search query sequences against the target sequences in filename, in fasta or fastq format. This option is mandatory.

core options

--dbmask none|dust|soft
Mask regions in the database sequences using the dust method or the soft method, or none to suppress masking. See vsearch-fastx_mask(1) for more details. Warning, when using soft masking, search commands become case sensitive. The default is to mask using dust.

--qmask none|dust|soft
Mask regions in query sequences using the dust method or the soft method, or none to suppress masking. Values are case-insensitive, so DUST, Dust, and dust are all accepted. See vsearch-fastx_mask(1) for more details. Warning, when using soft masking, search commands become case sensitive. The default is to mask using dust.

--strand plus|both
Check the plus strand only (default), or check both strands when comparing sequences.

--threads positive integer
Set the number of computation threads to use, from 1 to 1024. The number of threads should not exceed the number of available CPU cores. The default is to use all available cores.

secondary options

--alnout filename
Write pairwise global alignments to filename in a human-readable format. Use --rowlen to set the alignment line width.

--biomout filename
Write an OTU table to filename in the biom version 1.0 JSON file format. The OTUs are represented by the cluster centroids. Sample identifiers are extracted from sequence headers (;sample=abc123; or ;barcodelabel=abc123; patterns, or the initial part of the header). OTU identifiers are extracted from centroid headers (;otu=def789; pattern, or the initial part of the header, or via relabelling options). Taxonomy information is extracted from centroid headers (;tax=...; pattern) if available.

--blast6out filename
Write results to filename using a BLAST-like tab-separated format with twelve fields per query-target match: query label, target label, percentage identity, alignment length, mismatches, gap openings, query start, query end, target start, target end, expectation value (always -1), and bit score (always 0). If --output_no_hits is used, non-matching queries are also written. Note that vsearch uses global pairwise alignments, not BLAST’s seed-and-extend algorithm.

--bzip2_decompress
Specify that the input pipe is streaming data compressed using Huffman coding. See bzip2(1) for more details. This option is not needed when reading from a regular file compressed with bzip2.

--dbmatched filename
Write database target sequences that match at least one query sequence to filename, in fasta format. If --sizeout is specified, the number of matching queries is annotated in the header (;size=integer).

--dbnotmatched filename
Write database target sequences that do not match any query sequence to filename, in fasta format.

--fasta_width positive integer
Set the maximal width of sequences when writing fasta files. Longer sequences are folded and written on several lines. Default width is 80 nucleotides. Set to zero (0) to suppress folding.

--fastapairs filename
Write pairwise alignments of query and target sequences to filename, in fasta format.

--gzip_decompress
Specify that the input pipe is streaming data compressed using Lempel-Ziv coding. See gzip(1) for more details. This option is not needed when reading from a regular file compressed with gzip.

--hardmask
Replace masked nucleotides with Ns.

--label_suffix string
Add the suffix string to sequence headers when writing fasta or fastq files. For example, with --label_suffix ";status=healthy", sequence header ‘>seq1’ becomes ‘>seq1;status=healthy’.

--lca_cutoff real
Set the fraction of hits that must agree at a given taxonomic rank for that rank to be included in the last common ancestor (LCA) output (see --lcaout). The default value is 1.0, requiring all hits to agree. Lower values (e.g., 0.95) tolerate a small fraction of disagreeing hits. The value must be greater than 0.5 and at most 1.0.

--lcaout filename
Write last common ancestor (LCA) information to filename in a tab-separated format. The first column contains the query identifier and the second column contains the deepest taxonomic lineage shared by a sufficient fraction of hits (see --lca_cutoff). Database sequence headers must carry taxonomic annotations in the format used by --sintax (e.g., tax=k:Archaea,p:Euryarchaeota,c:Halobacteria). Set --maxaccepts to a value greater than 1 for the LCA to be meaningful.

--lengthout
Add a sequence length annotation (;length=integer) to each sequence header when writing fasta or fastq files.

--log filename
Write messages to filename. Messages include program version, start and finish times, elapsed time, amount of memory available, maximum amount of memory consumed, number of cores and command line options, and if need be, command-specific informational messages, warnings, and errors.

--matched filename
Write query sequences matching a target sequence to filename, in fasta format.

--maxhits non-negative integer
Set the maximum number of hits to report once the search is terminated for a given query; hits are sorted by decreasing identity. Unlimited by default, or when the argument is zero. When searching both strands, --maxhits controls the total number of hits reported per query across both strands.

--maxqsize positive integer
Reject query sequences with an abundance greater than integer.

--maxqt real
Reject the sequence match if the query/target sequence length ratio is greater than real.

--maxseqlength positive integer
Discard sequences longer than positive integer (50,000 nucleotides by default).

--maxsizeratio real
Reject the sequence match if the query/target abundance ratio is greater than real.

--maxsl real
Reject the sequence match if the shorter/longer sequence length ratio is greater than real.

--mincols positive integer
Reject the sequence match if the alignment length is shorter than integer columns.

--minqt real
Reject the sequence match if the query/target sequence length ratio is lower than real.

--minseqlength positive integer
Discard sequences shorter than positive integer (1 nucleotide by default).

--minsizeratio real
Reject the sequence match if the query/target abundance ratio is lower than real.

--minsl real
Reject the sequence match if the shorter/longer sequence length ratio is lower than real.

--mintsize positive integer
Reject target sequences with an abundance lower than integer.

--mothur_shared_out filename
Write an OTU table to filename in the mothur ‘shared’ tab-separated plain text format. The first line starts with label, group and numOtus, followed by all OTU identifiers. Each subsequent line starts with vsearch, the sample identifier, the total number of OTUs, and the abundance of each OTU in that sample. Sample and OTU identifiers are extracted from FASTA headers. OTUs are represented by the cluster centroids.

--no_progress
Suppress the gradually increasing progress indicator normally written to the standard error stderr(3).

--notmatched filename
Write the sequences that were not extracted to filename, in fasta format.

--notrunclabels
Retain whole sequence headers in output files. By default, vsearch truncates sequence headers at first space or tabulation. This option suppresses truncation.

--otutabout filename
Write an OTU table to filename in a classic tab-separated plain text format. The first line starts with #OTU ID followed by sample identifiers. Each subsequent line starts with the OTU identifier followed by the abundances in each sample. Sample and OTU identifiers are extracted from FASTA headers (see --sample). OTUs are represented by the cluster centroids. A taxonomy column is appended if taxonomy information is available for any OTU.

--output_no_hits
Write both matching and non-matching queries to --alnout, --blast6out, --samout, or --userout output files. Non-matching queries are labelled ‘No hits’ in --alnout files.

--qsegout filename
Write the aligned part of each query sequence to filename, in fasta format.

--quiet
Suppress messages to the standard output stdout(3) and standard error stderr(3), except for warnings and error messages.

--relabel string
Replace sequence headers with the prefix string and a ticker (1, 2, 3, etc.). For example, with --relabel "cluster:", the first sequence header becomes ‘>cluster:1’, the second sequence header becomes ‘>cluster:2’, and so on. To retain annotations, use their corresponding options (--lengthout, --eeout, and --sizeout). Use --relabel_keep to also retain old sequence identifiers.

--relabel_keep
Retain old sequence identifiers by including them at the end of the new headers, after a space.

--relabel_md5
Replace each sequence header with the MD5 digest derived from the sequence itself. The sequence is converted to upper case, and each ‘U’ is replaced with a ‘T’ before computation of the digest. The MD5 digest is a 128-bit value (16 bytes), represented using a string of 32 ASCII characters. Each pair of characters encodes an hexadecimal value, ranging from x00 to xff. See md5(3) for more details, and --relabel_sha1 for an alternative hashing algorithm. To retain annotations, use their corresponding options (--lengthout, --eeout, and --sizeout). Use --relabel_keep to also retain old sequence identifiers.

--relabel_self
Replace each sequence header with the sequence itself. To retain annotations, use their corresponding options (--lengthout, --eeout, and --sizeout). Use --relabel_keep to also retain old sequence identifiers.

--relabel_sha1
Replace each sequence header with the SHA1 digest derived from the sequence itself. The sequence is converted to upper case, and each ‘U’ is replaced with a ‘T’ before computation of the digest. The SHA1 digest is a 160-bit value (20 bytes), represented using a string of 40 ASCII characters. Each pair of characters encodes an hexadecimal value, ranging from x00 to xff. See sha1(3) for more details, and --relabel_md5 for an alternative hashing algorithm. To retain annotations, use their corresponding options (--lengthout, --eeout, and --sizeout). Use --relabel_keep to also retain old sequence identifiers.

--rowlen positive integer
Set the width of alignment lines in --alnout output. The default value is 64. Set to 0 to disable line wrapping.

--samheader
Include header lines (@HD, @SQ, @PG) in the SAM file produced by --samout. By default, no header lines are written.

--samout filename
Write alignment results to filename in the SAM format, see vsearch-sam(5). Use --samheader to include header lines. Each non-header line is a SAM record representing either a query-target alignment or the absence of a match. The alignment column of each record uses the CIGAR format, see vsearch-cigar(5).

--sample string
Add the given sample identifier string to sequence headers when writing fasta or fastq files. For instance, if string is ‘ABC’, the text ;sample=ABC will be added to the headers. string is silently truncated at the first ‘;’ or whitespace character (space, tab, newline, carriage return, vertical tab or form feed), so such characters should not be used in string. Other characters (alphabetical, numerical and punctuations) are accepted.

--self
Reject the sequence match if the query and target sequence labels are identical.

--sizein
Use the abundance annotations present in sequence headers when reading fasta or fastq file. Search for the pattern [>@;]size=integer[;]. Entries without abundance annotations are silently assumed to be of size=1.

--sizeout
Add abundance annotations to sequence headers when writing fasta or fastq files. Add the pattern ;size=integer. If option --sizein is not used, abundance values are set to 1 for all entries. If --sizein is used, existing abundance annotations are simply reported to output files.

--top_hits_only
Report only the hits with the highest pairwise identity for each query.

--tsegout filename
Write the aligned part of each target sequence to filename, in fasta format.

--uc filename
Write search results to filename in a tab-separated uclust-like format with 10 columns. Each query produces a hit (H) or no-hit (N) record. Use --uc_allhits to report all hits per query instead of just the top hit. Columns are:

  1. record type: H (hit) or N (no hit);
  2. ordinal number of the target sequence (zero-based; * for N);
  3. length of the query sequence (* for N);
  4. percentage of identity with the target (* for N);
  5. match orientation + or - (. for N);
  6. not used; 0 (H) or * (N);
  7. not used; 0 (H) or * (N);
  8. CIGAR alignment string (* for N); see vsearch-cigar(5);
  9. query label;
  10. target label (* for N).

--uc_allhits
When using --uc, report all hits for each query, not just the top hit.

--userfields string
Select and order the fields written to --userout output. Fields are separated by + (e.g. query+target+id). See vsearch-userfields(7) for a complete description of all available fields.

--userout filename
Write user-defined tab-separated output to filename. Select and order the fields with --userfields.

--xee
Strip expected error (ee) annotations from sequence headers when writing fasta or fastq files. Search for the pattern [>@;]ee=float[;]. Expected error annotations are added by the synonymous options --fastq_eeout and --eeout described in vsearch-fastx_filter(1).

--xlength
Strip sequence length annotations from sequence headers when writing fasta or fastq files. Search for the pattern [>@;]length=integer[;]. Sequence length annotations are added by the --lengthout option.

--xsize
Strip abundance annotations from sequence headers when writing fasta or fastq files. Search for the pattern [>@;]size=integer[;]. Abundance annotations are added by the --sizeout option.

pairwise alignment options

These options modify the pairwise alignment scoring model used when writing alignment output (e.g., --alnout). Modify with caution.

--match integer
Set the score assigned to a match (i.e. equivalent nucleotides) in pairwise alignments. The default value is 2.

--mismatch integer
Set the score assigned to a mismatch (i.e. different nucleotides) in pairwise alignments. The default value is -4.

EXAMPLES

Find all exact matches in a database and write results in BLAST-like tabular format:

vsearch \
    --search_exact queries.fasta \
    --db reference.fasta \
    --blast6out results.tsv

Search both strands and write matching and non-matching queries to separate fasta files:

vsearch \
    --search_exact queries.fasta \
    --db reference.fasta \
    --strand both \
    --matched exact_hits.fasta \
    --notmatched no_hits.fasta

Build an OTU table by mapping dereplicated reads to OTU centroids using exact matching:

vsearch \
    --search_exact reads.fasta \
    --db otus.fasta \
    --otutabout otu_table.tsv \
    --threads 8

SEE ALSO

vsearch-usearch_global(1), vsearch-cigar(5), vsearch-fasta(5), vsearch-fastq(5), vsearch-userfields(7)

CITATION

Rognes T, Flouri T, Nichols B, Quince C, Mahé F. (2016) VSEARCH: a versatile open source tool for metagenomics. PeerJ 4:e2584 doi: 10.7717/peerj.2584

REPORTING BUGS

Submit suggestions and bug-reports at https://github.com/torognes/vsearch/issues, send a pull request on https://github.com/torognes/vsearch, or compose a friendly or curmudgeont e-mail to Torbjørn Rognes (torognes@ifi.uio.no).

AVAILABILITY

Source code and binaries are available at https://github.com/torognes/vsearch.

COPYRIGHT

Copyright (C) 2014-2026, Torbjørn Rognes, Frédéric Mahé and Tomás Flouri

All rights reserved.

Contact: Torbjørn Rognes torognes@ifi.uio.no, Department of Informatics, University of Oslo, PO Box 1080 Blindern, NO-0316 Oslo, Norway

This software is dual-licensed and available under a choice of one of two licenses, either under the terms of the GNU General Public License version 3 or the BSD 2-Clause License.

GNU General Public License version 3

This program is free software: you can redistribute it and/or modify it under the terms of the GNU General Public License as published by the Free Software Foundation, either version 3 of the License, or (at your option) any later version.

This program is distributed in the hope that it will be useful, but WITHOUT ANY WARRANTY; without even the implied warranty of MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the GNU General Public License for more details.

You should have received a copy of the GNU General Public License along with this program. If not, see http://www.gnu.org/licenses/.

The BSD 2-Clause License

Redistribution and use in source and binary forms, with or without modification, are permitted provided that the following conditions are met:

  1. Redistributions of source code must retain the above copyright notice, this list of conditions and the following disclaimer.

  2. Redistributions in binary form must reproduce the above copyright notice, this list of conditions and the following disclaimer in the documentation and/or other materials provided with the distribution.

THIS SOFTWARE IS PROVIDED BY THE COPYRIGHT HOLDERS AND CONTRIBUTORS “AS IS” AND ANY EXPRESS OR IMPLIED WARRANTIES, INCLUDING, BUT NOT LIMITED TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE ARE DISCLAIMED. IN NO EVENT SHALL THE COPYRIGHT HOLDER OR CONTRIBUTORS BE LIABLE FOR ANY DIRECT, INDIRECT, INCIDENTAL, SPECIAL, EXEMPLARY, OR CONSEQUENTIAL DAMAGES (INCLUDING, BUT NOT LIMITED TO, PROCUREMENT OF SUBSTITUTE GOODS OR SERVICES; LOSS OF USE, DATA, OR PROFITS; OR BUSINESS INTERRUPTION) HOWEVER CAUSED AND ON ANY THEORY OF LIABILITY, WHETHER IN CONTRACT, STRICT LIABILITY, OR TORT (INCLUDING NEGLIGENCE OR OTHERWISE) ARISING IN ANY WAY OUT OF THE USE OF THIS SOFTWARE, EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE.

ACKNOWLEDGMENTS

We would like to thank the authors of the following projects for making their source code available: