NAME

vsearch \-\-fastx_mask — mask low-complexity regions in fasta or fastq sequences

SYNOPSIS

vsearch \-\-fastx_mask fastxfile (\-\-fastaout | \-\-fastqout) filename [options]

DESCRIPTION

The vsearch command --fastx_mask masks low-complexity regions and simple repeats in sequences from a fasta or fastq file. The input format is detected automatically (see vsearch-fasta(5) and vsearch-fastq(5)).

Masking is controlled with the --qmask option, which accepts three values: dust (default), soft, or none. With dust, low-complexity regions are identified with the DUST algorithm (R. Tatusov and D.J. Lipman, unpublished) and represented as lowercase letters in the output. With soft, lowercase letters in the input are treated as masked and preserved as-is. With none, no masking is applied.

By default, masked regions are written as lowercase letters (soft masking). When --hardmask is specified, masked regions are replaced with N’s instead.

Sequences can be filtered by the proportion of unmasked residues after masking. Use --min_unmasked_pct to discard sequences with too few unmasked residues, and --max_unmasked_pct to discard those with too many.

At least one output option must be specified: --fastaout and/or --fastqout. The --fastqout option requires fastq input.

This command supersedes --maskfasta (see vsearch-maskfasta(1)), which is restricted to fasta input.

To illustrate the effect of DUST masking on a fasta file:

Input:                    --qmask dust:             --qmask dust --hardmask:

>s1                       >s1                       >s1
AAAAAAAAACGTACGT   -->    aaaaaaaaACGTACGT   -->    NNNNNNNNACGTACGT
>s2                       >s2                       >s2
ACGTACGTACGTACGT          ACGTACGTACGTACGT          ACGTACGTACGTACGT

OPTIONS

mandatory options

At least one of the following output options must be specified:

--fastaout filename
Write masked sequences to filename, in fasta format.

--fastqout filename
Write masked sequences to filename, in fastq format (see vsearch-fastq(5)). Requires fastq input.

core options

masking

--hardmask
Replace masked nucleotides with Ns.

--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.

filtering

--max_unmasked_pct real
Discard sequences with more than real percent of unmasked residues.

--min_unmasked_pct real
Discard sequences with less than real percent of unmasked residues.

secondary options

--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.

--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.

--fastq_ascii 33|64
Specify the offset used as the basis for the fastq quality score when reading fastq files. For example, an offset of 33 means that a quality value of 41 is represented by the 74th ASCII symbol (33 + 41 = 74), which is ‘J’. See ascii(7) for a view of the ASCII character set. The offset value is either 33 or 64, default is 33.

--fastq_qmax positive integer
Specify the maximal quality score accepted when reading fastq sequences. Stop with an error message if a quality score higher than the specified value is read. Accepted values range from 0 to 93 if the offset is 33 (see --fastq_ascii), or range from 0 to 62 if the offset is 64. The default is 41, which is usual for recent Sanger/Illumina 1.8+ files.

--fastq_qmin positive integer
Specify the minimal quality score accepted when reading fastq sequences. Stop with an error message if a quality score lower than the specified value is read. Accepted values range from 0 to 93 if the offset is 33 (see --fastq_ascii), or range from 0 to 62 if the offset is 64. The default is 0, which is usual for recent Sanger/Illumina 1.8+ files. Older formats may use scores between -5 and 2.

--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.

--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’.

--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.

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

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

--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.

--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.

--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.

--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.

--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.

EXAMPLES

Mask low-complexity regions in a fasta file using the DUST algorithm (default), and write the results to masked.fasta:

vsearch \
    --fastx_mask input.fasta \
    --fastaout masked.fasta

Replace masked regions with N’s instead of lowercase letters (--hardmask), and write the results to masked.fasta:

vsearch \
    --fastx_mask input.fasta \
    --hardmask \
    --fastaout masked.fasta

Mask a fastq file and discard sequences where more than 50% of residues are unmasked (i.e., retain only highly repetitive sequences):

vsearch \
    --fastx_mask input.fastq \
    --max_unmasked_pct 50.0 \
    --fastqout masked.fastq

Mask a fasta file and discard sequences where fewer than 80% of residues are unmasked (i.e., retain only sequences with sufficient complexity):

vsearch \
    --fastx_mask input.fasta \
    --min_unmasked_pct 80.0 \
    --fastaout masked.fasta

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

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:

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

vsearch includes code from Google’s CityHash project by Geoff Pike and Jyrki Alakuijala, providing some excellent hash functions available under a MIT license.
vsearch includes code derived from Tatusov and Lipman’s DUST program that is in the public domain.
vsearch includes public domain code written by Alexander Peslyak for the MD5 message digest algorithm.
vsearch includes public domain code written by Steve Reid and others for the SHA1 message digest algorithm.
vsearch binaries may include code from the zlib library, copyright Jean-Loup Gailly and Mark Adler.
vsearch binaries may include code from the bzip2 library, copyright Julian R. Seward.

vsearch

Versatile open-source tool for microbiome analysis