The Gene Indices Sequence Cleaning and Validation script (SeqClean)
3.Usage and methods
SeqClean is a tool for validation and trimming of DNA sequences from a flat
file database (FASTA format). SeqClean was designed primarily for "cleaning"
of EST databases, when specific vector and splice site data are not
available, or when screening for various contaminating sequences is desired.
The program works by processing the input sequence file and filtering its
content according to a few criteria:
* percentage of undetermined bases
* polyA tail removal
* overall low complexity analysis
* short terminal matches with various sequences used
during the sequencing process (vectors, adapters)
* strong matches with other contaminants or unwanted sequences
(mitochondrial, ribosomal, bacterial, other species than the
target organism etc.)
The user is expected to provide the contaminant databases,
they are not included in this package.
* perl version >= 5.6
* a working installation of recent versions of NCBI's
blastall and megablast programs (
* one or more databases of potential contaminants (e.g. a vector
database like NCBI's UniVec) properly formatted to work with
NCBI's blastall (using formatdb)
A binary distribution for this package is provided for Linux ix86 systems
with glibc >=2.1. NCBI's blastall and megablast are not included,
they should instead be obtained directly from NCBI.
The source code of the various other tools included in the package
is provided so they can be compiled on other Unix platforms
where NCBI's tools work.
Create a directory where you plan the package to reside.
Copy the compiled archive into that directory and unpack the archive
tar xvfz seqclean.tar.gz
This will unpack a few files in the current directory
and will create a bin subdirectory with several files.
The program to run is seqclean script from the main directory.
When launched, this program will prefix the local ./bin
subdirectory to the shell's path. Optionally, you may move/copy
all binaries and scripts from ./bin subdirectory somewhere
in your working shell PATH. You can also copy the main script
(seqclean) to your preferred script location (which should be in the
shell's PATH), in which case the module Mailer.pm should go in the
same directory with the tgicl script or into a one of the PERLLIB
There are 2 perl scripts in this package:
They all have the perl location as the first line, set to
If this is not the valid path for your perl installation
you need to change these lines in all three files,
to point to your actual perl binary location.
3.Usage and methods
A short usage message is displayed when seqclean script is launched without
The seqclean script takes an input sequence file (fasta formatted) as the only
seqclean creates two output files of interest:
1. the filtered FASTA file (your_est_file.clean for the example above)
containing only valid (non-trashed) and trimmed ("clear range") sequences
2. a "cleaning report" (your_est_file.cln) providing details about
sequence trimming and trashing (coordinates, reasons for trashing,
contaminant names etc. - see below for a detailed description).
However, the simple usage example above will not perform any searches
against contaminant databases (as there are none specified) but it will
only provide basic analysis, removing the polyA/polyT tail, possibly
clipping low-quality ends (the ends rich in undetermined bases)
and trashing the ones which are too short (shorter than 100 or
the -l parameter value) or which appear to be mostly low-complexity
As suggested in the "Introduction", the contaminant databases provided
by the user can be considered to be of two types:
1. vector/adapter databases, which can determine the trimming
of the analyzed sequences even when only very short terminal matches
(down to 12 base pairs) are found. These database files should
be provided with the -v option (vector detection)
2. extensive contaminants databases: the alignments between these
contaminants and the analyzed sequences are only considered if
they are longer than 60 base pairs with at least 94% identity; these
are provided with the -s option (screening for contamination)
In both cases the analyzed sequences will be searched against the provided
files and the overlaps are analyzed. The contaminant databases should be
all formatted as required for blastall (using NCBI's formatdb program).
In the first case (vector/linker scan), the overlaps are only considered
if they are above 92% identity, they have very short gaps and they are
located in the 30% distance from either end. Also, the shorter these
overlaps are, the closer to either end of the analyzed sequence they
should be, in order to be considered for trimming of the target sequence.
Multiple vector/adapter databases can be provided at the -v option, separated
by comma (do not use spaces around the comma). Example:
seqclean your_est_file -v /usr/db/UniVec,/usr/db/adaptors,/usr/db/linkers
In this example three database files are checked for short terminal
matches with the analyzed sequences from "your_est_file".
The -s option case 2. above) works in a similar way, as more than one file can
be provided, but in that case only larger, statistically more significant
hits are considered. Example:
seqclean your_est_file -v /usr/db/UniVec,/usr/db/linkers \
In both cases, the contaminant database files should be provided with
their full path unless they can be found in the current working directory.
The searches against "-v" files are performed using blastall (blastn) with
low stringency, while for "-s" provided files, megablast is used, for
very fast screening. By default, the "smart" low-complexity filter is used
during both type of searches (the -F "m D" option of blastall/megablast).
However, in some cases, short vector/adaptor terminal overlaps might
be expected in regions of low-complexity, so the dust filter can be
disabled completely for any database file given at the "-v" option,
by appending the "^" character at the end of the file name:
seqclean your_est_file -v /usr/db/adapters^,/usr/db/UniVec,/usr/db/linkers^ \
In the example above, the "dust" filter is totally disabled for blastn
searches against /usr/db/adapters and /usr/db/linkers, while for the
other files (/usr/db/UniVec) it will still be set to work in "smart"
mode as mentioned above.
The cleaning scripts keep track of iterative trimming of the input
sequences through multiple matches with various contaminants,
if that's the case.The 5' end (end5) coordinate of each input sequence
is initially set to 1, and the 3' end (end3) coordinate is considered
to be the length of the initial sequences. During the above mentioned
trimming procedures, end5 can be increased and/or end3 can be decreased.
The final end3-end5+1 range is considered to be the "clear range" of the
sequence after going through the cleaning procedure. No matter if trimming
was applied or not, if the "clear range" length is shorter than a minimum
value (default 100nt, can be set by -l option), the sequence will
be considered invalid and it will be trashed. Also, at the end of
the cleaning procedure, the percentage of undetermined bases from the
clear range is computed and the sequence is also trashed if this
percentage is larger than 3%.
Cleaning report format
Each line in the cleaning report file (*.cln) has 7 tab-delimited fields
1. the name of the input sequence
2. the percentage of undetermined bases in the clear range
3. 5' coordinate after cleaning
4. 3' coordinate after cleaning
5. initial length of the sequence
6. trash code
7. trimming comments (contaminant names, reasons for trimming/trashing)
The trash code field (6) should be empty if (part of) a sequence is
considered valid - so it can be found in the final filtered file (*.clean)
The trash code field will be set to the file name of the last contaminant
database, if that determined the clear range to fall below the minimum value
(-l parameter, default 100). There are three reserved values of
the trash code:
"shortq" - assigned when the sequence length decreases
below the minimum accepted length (-l) after polyA
or low quality ends trimming;
"low_qual" - assigned when the percentage of undetermined bases
is greater than 3% in the clear range;
"dust" - assigned when less than 40nt of the sequence
is left unmasked by the "dust" low-complexity filter;
The reasons and the coordinates for trimming are mentioned in the 7th
field. When trimming was due to a contaminant match, the contaminant
name and the overlap coordinates are mentioned. When trimming was due
to polyA tail or low quality ends removal, the "trimpoly" program name is
mentioned along with the trimming coordinates.
Besides the -s and -v parameters mentioned above, here is a brief summary
of the other parameters:
-c : enables parallel processing by specifying the number of local CPUs
to use (for a SMP machine) or a filename containing a list of PVM node
names (one host name per line, per CPU). In the PVM case, if a node
is also a SMP machine and you want to use more than one CPU on that
node, you should list that same node name as many times as many CPUs
you want to use on that node. If this option is not provided,
only one CPU is used on the local machine.
-n : the input file is not usually processed as one single query file.
Instead, it is sliced up into little parts and each part
is processed separately; this option is useful to tweak when
you also make use of the multi-CPU option (-c), as each slice can
be processed by one CPU.
-l : the minimum accepted length of the clear range in order
to be considered valid. If the length of the clear range falls
below this value, a trash code is assigned to the input sequence
and it will be exclued from the output filtered file (*.clean)
-r : custom name of the cleaning report file (default: add the ".cln"
suffix to the input file name)
-o : custom name of the final "clear range"-only FASTA file containing only
the valid sequences (default: append ".clean" suffix to the
input file name)
-x : set the minimum percent identity to be considered for an
alignment with a contaminant (default 96)
-y : minimum length of a terminal vector hit to be considered
(>11, default 11)
-N : disable any attempt of trimming of low quality ends (ends rich in
N = undetermined bases)
-M : completely disable trashing of low quality (N-rich) sequences
-A : disable trimming of polyA tails from 3' end or polyT from 5' end of
the input sequences
-L : disable low-complexity analysis and the trashing of input sequences
by this criterion
-I : do not rebuild the .cidx file (if already there)
-m : enable sending of e-mail notification to the mentioned address, at
the end of the cleaning process or in case of error
If after seqclean one needs to trim the corresponding quality values too,
according to the new coordinates or trash codes found by seqclean, the
utility script "cln2qual" is included (see the usage message). It expects
a fasta-like file containing space delimited quality values for each nucleotide of
the original sequences. It should be run after the seqclean, as it parses the
trimming ("clear range") coordinates and trash codes from the cleaning report
and applies them to the quality records.
Copyright (c) 2005-2006, Dana-Farber Cancer Institute, All Rights Reserved
This software is OSI Certified Open Source Software.
OSI Certified is a certification mark of the Open Source Initiative.
For problems or questions related to the tools included in this package
please contact Geo Pertea at email@example.com