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项目作者： alexdonath

项目描述 ：
Finding outlier sequences in amino acid multiple sequence alignments.
高级语言： Perl
项目地址: git://github.com/alexdonath/checker_complete-v2.git
创建时间： 2020-05-27T11:31:22Z
项目社区：https://github.com/alexdonath/checker_complete-v2
开源协议：GNU General Public License v3.0
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checker_complete.2.pl

Finding outlier sequences in amino acid multiple sequence alignments.

Table of Contents

General description

checker_complete.2.pl is a complete reimplementation of the outlier check routine provided by the checker_complete.1.3.x.2.pl scripts. It includes a number of changes, bug fixes, and improvements, such as the possibility to define arbitrary reference sets for the outlier distance calculation (for a detailed list of fixes and improvements, see below).

The script offers two different execution modes. The default mode allows the definition of arbitrary reference sequence sets and subject sequence sets, respectively. The 1KITE compatibility mode defines reference and subject species based on the FASTA headers in the alignment (two pipe symbols | for reference species, three for subject species) and integrates flawlessly in the current 1KITE pipeline.

Usage

How to use checker_complete.2.pl is probably best explained with a few examples.

Calling checker_complete.2.pl without any parameters (or -h), will show all available options:

  1. $ ./checker_complete.2.pl
  3. Usage: ./checker_complete.2.pl -a alignment(s) [further options]
  5. Options:
  6.       -a    Path to alignment file(s)
  7.             [Required]
  9.       -s    Path to file with taxa of interest to test
  11.       -r    Path to reference taxa file
  13.       -k    Ensure 1KITE compatible input and output
  15.       -m    Substitution matrix [possible values: b62|b80|b62n|b80n]
  16.             [Default: b62 (= original BLOSUM62 matrix)]
  18.             WARNING: b62n and b80n are not tested.
  20.       -l    Name of log file
  21.             [Default: log.txt]
  23.       -o1   Name of first output file
  24.             [Default: outlier_1.txt]
  26.             Contains for each alignment a list of outlier taxa and
  27.             their distance score.
  29.     -o2     Name of second output file
  30.             [Default: outlier_2.txt]
  32.             Contains for each alignment a list of outlier FASTA
  33.             headers.
  35.     -h      Print this help message
  37.     -v      Print version

The only required input is one or more alignment file(s) that should be checked for outlier sequences (option: -a). Additionally, depending on the execution mode, you can provide a file to the script that lists the headers of all sequences you would like to use as reference taxa (option: -r) and/or a file that contains the headers of all sequences you would like to filter (i.e., the subject file; option: -s). The content of the subject file is explained in detail below.

Input

Default mode

The script only requires the name of one or several alignment files that should be checked for outliers. Reference sequences and subject sequences are then deduced automatically based on the name of the alignment file. For example, calling the script with an alignment file name EOG090X002.aa.fa

  1. checker_complete.2.pl -a EOG090X002.aa.fa

assumes the presence of a file called EOG090X002.aa.fa.refs that contains the sequence headers (without the > symbol) of all taxa that should be used as reference species. All remaining sequences in the alignment will be treated as subject sequences and searched for outlier sequences.

You can, however, provide a reference sequence file explicitly (option: -r):

  1. checker_complete.2.pl -a EOG090X002.aa.fa -r my.refs.txt

In this case, the sequences in EOG090X002.aa.fa that belong to the sequence headers provided in the file my.refs.txt (without the > symbol) will be used as reference species. All remaining sequences in the alignment will be treated as subject sequences and searched for outlier sequences.

You can modify this behavior by providing a list of FASTA headers of those subject sequences (option: -s) you would like to test:

  1. checker_complete.2.pl -a EOG090X002.aa.fa -r my.refs.txt -s subjects.txt

Here, the sequences in EOG090X002.aa.fa that belong to the sequence headers provided in the file my.refs.txt will be used as reference species and all sequences with their FASTA headers listed in subjects.txt that are present in the alignment file (EOG090X002.aa.fa) will be checked for outliers.

Checking multiple files

checker_complete.2.pl supports the use of wildcards to check multiple alignment files in the same run:

  1. checker_complete.2.pl -a EOG*.aa.fa

This will check all alignments found in files that match the pattern EOG*.aa.fa for outlier sequences. For each alignment file, the script requires the presence of a file called EOG*.aa.fa.refs that contains the sequence headers of all taxa which should be used as reference species for this specific alignment. For example, given two alignment files called EOGxxx.aa.fa and EOGyyy.aa.fa, the script requires the presence of two additional files EOGxxx.aa.fa.refs containing the reference sequence headers for EOGxxx.aa.fa and EOGyyy.aa.fa.refs containing the reference sequence headers for EOGyyy.aa.fa, respectively. All other sequences in the respective alignment will be treated as subject sequences and searched for outlier sequences.

If you want to check multiple alignment files and the FASTA headers of all reference taxa are identical between alignment files, you can also provide a single reference file that contains these headers (option: -r):

  1. checker_complete.2.pl -a EOG*.aa.fa -r my.universal.refs.txt

All other sequences in the respective alignment will be treated as subject sequences and searched for outlier sequences.

In default mode, the following algorithmic decisions are enforced:

  1. The reference species file should contain the full FASTA headers (without the > symbol) of the sequences in the alignment that should be treated as reference species.

  2. If a subjects file is provided, it is assumed that it contains the full FASTA header (without the > symbol) of the sequences that should be checked for outliers.
    If no subject file is provided, all sequences in the alignment that are not present in the reference species list are used as subject sequences.

  3. The BLOSUM distances (see below) of the amino-acid sequences of all reference species are calculated. Based on these distances, a cut-off value is derived. After that, for each transcript (subject) sequence the minimal BLOSUM distance to any of the reference taxa is calculated. Sequences with a minimal BLOSUM distance to their closest reference species larger than the cut-off value are classified as outliers.

  4. The output format of the first output file (option: -o1) will be different to the format originally provided by checker_complete.1.3.1.2.pl. The content, however, is similar.

1KITE compatibility mode

This mode is enforced by using the -k flag:

  1. checker_complete.2.pl -a EOG090X002.aa.fa -s subjects.txt -k

This will change the algorithm in several ways:

  1. A subject file that now only contains the name of all transcriptome taxa as written in the third field (see below) is now mandatory.

  2. Reference species in the alignment are automatically identified based on the number of pipe symbols (|) in their sequence header (i.e., two pipe symbols, see next point).

  3. The FASTA headers of the sequences in the alignment are required to be in HaMStrad format, i.e. reference species headers have two pipe symbols (e.g., >EOGxyz|reference_taxon_name|GenID) and all subject (transcriptome) sequence headers have three pipe symbols (e.g., >EOGxyz|reference_taxon_name|subject_taxon_name|contig-header).

  4. As in default mode, the BLOSUM distances of the amino-acid sequences of all reference species are calculated. Based on these distances, the cut-off value is determined. After that, the BLOSUM distance of each transcript (subject) sequence to the corresponding sequence of the reference taxon found as best reciprocal hit during orthology assignment (reference_taxon_name) is calculated. Sequences with a minimal BLOSUM distance to their reference species larger than the cut-off value are classified as outliers.

  5. The output format of the first output file (option: -o1) will be compatible to the format provided by the original checker_complete.1.3.1.2.pl script. This will ensure that existing scripts in the 1KITE community that make use of this file for further downstream analyses don’t need to be modified.

Requesting the 1KITE compatibility mode and providing a reference species list simultaneously, will result in an error:

  1. $ checker_complete.2.pl -a EOG090X002.aa.fa -s subjects.txt -k -r my.refs
  2. [ERROR] Contradictory settings. 1KITE-compatibility requested and reference file given.

Content of the subjects file

Default mode

In default mode, the subjects file is optional. If it is provided, however, it must contain the full FASTA header (without the > symbol) of the sequences that should be checked for outliers. For example, given the following FASTA headers in the alignment file:

  1. >EOG508HX6|BMORI_3.2|Tricholepidion_gertschi|C20406_l5235
  2. >EOG508HX6|BMORI_3.2|Drosophila_melanogaster|C20406_l6733
  3. ...

The content of the subjects file must be:

  1. EOG508HX6|BMORI_3.2|Tricholepidion_gertschi|C20406_l5235
  2. EOG508HX6|BMORI_3.2|Drosophila_melanogaster|C20406_l6733

If no subjects file is provided, all sequences in the alignment that are not present in the reference species list are used as subject sequences.

1KITE compatibility mode

In this mode, the subjects file must only contain the name of all transcriptome taxa as written in the third field of their sequence headers, one taxon name per line. For example, given the following sequence headers in the alignment file:

  1. >EOG508HX6|BMORI_3.2|Tricholepidion_gertschi|C20406_l5235
  2. >EOG508HX6|BMORI_3.2|Drosophila_melanogaster|C20406_l6733
  3. ...

The content of the subjects file must be:

  1. Tricholepidion_gertschi
  2. Drosophila_melanogaster

Substitution matrix

As in previous instances of this script, checker_complete.2.pl uses the BLOSUM62 log-odds matrix for the sequence distance calculation. However, the BLOSUM62 matrix might not be appropriate for very similar sequences. Thus, the BLOSUM80 matrix is also supported now and can be requested with the -m option:

  1. checker_complete.2.pl -a EOG090X002.aa.fa -s subjects.txt -m b80

Note that the script also supports the updated versions of the original BLOSUM62 and BLOSUM80 matrices, respectively (b62n and b80n, respectively). However, their use is currently experimental and may not be include in future versions of this script.

Output

The original checker_complete.1.3.1.2.pl and checker_complete.1.3.2.2.pl scripts differed only in their output. Both created identical (and therefore redundant) log files (log_1.txt and log_2.txt, respectively) that contained various details about the analyzed alignment:

  • The name of the alignment file,
  • the alignment length,
  • the missing subject sequences,
  • the total number of taxa in the alignment,
  • the number of transcriptome (subject) sequences,
  • the sequence overlap length,
  • the minimum and maximum distance values,
  • the median, the lower (Q1) and upper (Q3) quartile,
  • the outlier cutoff,
  • the BLOSUM62 distance and relative BLOSUM62 distance to the closest reference taxon (during orthology assignment step),
  • whether a sequence was classified as outlier,
  • the number of outliers in the alignment,
  • the total number of checked alignments, and
  • the total number of files with outliers.

Additionally, both scripts created an outlier file. The outlier file created by checker_complete.1.3.1.2.pl (called outlier_1.txt) contained a reduced set of information:

  • The name of the alignment file,
  • the minimum and maximum distance values,
  • the median, the lower (Q1) and upper (Q3) quartile,
  • the BLOSUM62 distance and relative BLOSUM62 distance to the closest reference taxon (during orthology assignment step), and
  • the name of the sequences that were classified as outlier.

The outlier file created by checker_complete.1.3.2.2.pl (called outlier_2.txt) contained only:

  • The name of the alignment file and
  • the complete sequence headers of those sequences that were classified as outlier.

checker_complete.2.pl now creates all three files (a single log file and both outlier files) simultaneously. To ensure compatibility to existing 1KITE workflows, the default names of these files are log.txt, outlier_1.txt, and outlier_2.txt. All names, however, can be modified by the user:

  1. checker_complete.2.pl -a file.fas -l my.log -o1 outlier1.log -o2 outlier2.log

Test data

To test whether checker_complete.2.pl works as intended, some examples files are
provided in the example directory. To analyse the test data, simply change into the directory and execute the runMe.sh script:

  1. cd example
  2. chmod +x runMe.sh
  3. ./runMe.sh

History/List of changes

v 2.0.1

June 25, 2020

Changes/Improvements:

  • If all sequences are reference sequences and no list of subject sequences was given, automatic identification of subject sequenced is not possible. A list of subjects is now required in these cases.
  • Minor code cleanup.

v 2.0.0b - First release

May 27, 2020

This is the first release of the reimplementation of the checker_complete.1.3.x.2.pl scripts by Bernhard Misof. Major changes and resolved bugs are:

Changes/Improvements:

  • Arbitrary sets for reference taxa and taxa to test can now be provided by the user
  • BLOSUM80 can now be used for distance calculation
  • Outlier calculation is now based on the interquartile range (IQR)
  • File names for log files and outlier files can now be selected by the user
  • Output files of checker_complete.1.3.1.2.pl and checker_complete.1.3.2.2.pl are now created simultaneously
  • Output files are not overwritten

Bugs fixed:

  • Now works with newer PERL versions
  • Quartile calculation was inconsistent
  • Not all reference taxa were included in the output
  • Smallest distance between reference taxa was not calculated correct

If you find the checker_complete.2.pl script useful for you work, please consider citing:

Karmeinski D, Meusemann K, Goodheart JA, Schroedl M, Martynov A, Korshunova T, Wägele H, Donath A. 2021. Transcriptomics provides a robust framework for the relationships of the major clades of cladobranch sea slugs (Mollusca, Gastropoda, Heterobranchia), but fails to resolve the position of the enigmatic genus Embletonia. BMC Ecology and Evolution 21:226. https://doi.org/10.1186/s12862-021-01944-0

checker_complete.2.pl is published under the GPLv3.

checker_complete.2.pl is a reimplementation of the two scripts checker_complete.1.3.1.2.pl and checker_complete.1.3.2.2.pl originally written by Bernhard Misof (zmb, ZFMK) and published under the GNU General Public License version 2 (or any later version).

Both scripts were published in:

Misof B, Liu S, Meusemann K, Peters RS, Donath A, Mayer C, Frandsen PB, Ware J, Flouri T, Beutel RG, et al. 2014. Phylogenomics resolves the timing and pattern of insect evolution. Science 346:763-767. https://doi.org/10.1126/science.1257570