seqfilter

Filter out sequences based on specified criterion

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Syntax

seqfilter(fastqFile)
seqfilter(fastqFile,Name,Value)
[outFiles,nSeqIn,nSeqOut] = seqfilter(___)

Description

example

seqfilter(fastqFile) applies a filtering criterion to the sequences in fastqFile and saves the sequences that meet the criterion in a new FASTQ file. By default, the sequences that pass the criterion are saved under file names with the suffix '_filtered' appended. If you do not specify any criterion, the function filters sequences using the default.

example

seqfilter(fastqFile,Name,Value) uses additional options specified by one or more Name,Value pair arguments.

[outFiles,nSeqIn,nSeqOut] = seqfilter(___) returns a cell array outFiles with the names of output files. nSeqIn and nSeqOut represent the numbers of sequences included and excluded from each input file, respectively.

Examples

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Open Live Script

Filter out sequences with more than 10% of low quality bases, where a base is considered low quality when its quality score is less than 20.

 [outFile,in,out] = seqfilter('SRR005164_1_50.fastq',...
                              'Method','MaxPercentLowQualityBases',...
                              'Threshold',[10 20]) ;

Check the number of sequences saved in the output file.

in
in = 39

Check the number of sequences filtered out.

out
out = 11

Filter out sequences having an average quality score of below 20.

[outFile,in,out] = seqfilter('SRR005164_1_50.fastq',...
                             'Method','MeanQuality',...
                             'Threshold',20);

Apply the filtering criterion to every 10 bases as a sliding window.

[outFile,in,out] = seqfilter('SRR005164_1_50.fastq',...
                             'Method','MeanQuality',...
                             'Threshold',20,'WindowSize',10);

Filter out sequences with less than 100 bases.

[outFile,in,out] = seqfilter('SRR005164_1_50.fastq',...
                             'Method','MinLength',...
                             'Threshold',100);

Input Arguments

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Names of FASTQ-formatted files with sequence and quality information, specified as a character vector, string, string vector, or cell array of character vectors.

Example: 'SRR005164_1_50.fastq'

Name-Value Pair Arguments

Specify optional comma-separated pairs of Name,Value arguments. Name is the argument name and Value is the corresponding value. Name must appear inside quotes. You can specify several name and value pair arguments in any order as Name1,Value1,...,NameN,ValueN.

Example: 'Method','MaxNumberLowQualityBases','Threshold',[5 15] specifies to filter out sequences with a total of more than 5 low-quality bases, where a base is considered a low-quality base if its quality score is less than 15.

Criterion to filter sequences, specified as one of the following options. Specify only one filtering criterion per function call.

  • 'MaxNumberLowQualityBases'– applies a maximum threshold on the number of low-quality bases allowed.

  • 'MaxPercentLowQualityBases'– applies a maximum threshold on the percentage of low-quality bases allowed.

  • 'MeanQuality'– applies a minimum threshold on the average base quality across each sequence.

  • 'MinLength'– applies a minimum threshold on the sequence length.

Use this name-value pair argument together with 'Threshold' to specify the appropriate threshold value. Depending on the filtering criterion, the corresponding value for 'Threshold' can be a scalar or two-element vector. See the 'Threshold' option for the default values. If you do not specify 'Threshold', then the function uses the default threshold value of the specified method. For each filtering criterion, the function uses the base quality encoding format specified by the 'Encoding' name-value pair argument.

Example: 'Method','MaxNumberLowQualityBases','Threshold',[5 15]

Threshold value for the filtering criterion, specified as a scalar or vector. Use this name-value pair to define the threshold value for the filtering criterion specified by 'Method'.

Depending on the filtering criterion, the corresponding value for 'Threshold' can be a scalar or two-element vector. If you do not specify 'Threshold', then the function uses the default threshold value of the corresponding method. For each filtering criterion, the function uses the encoding format of the base quality specified by the 'Encoding' name-value pair argument.

'Method''Threshold'Default 'Threshold' value
'MaxNumberLowQualityBases'Two-element vector [V1 V2]. V1 is a nonnegative integer that specifies the maximum number of low-quality bases allowed. V2 specifies the minimum base quality. Any base with quality less than V2 is considered a low-quality base. Any sequence containing a number of low-quality bases greater than V1 is filtered out and not saved in the output file.[0 10]
'MaxPercentLowQualityBases'Two-element vector [V1 V2]. V1 is a scalar between 0 and 100 that specifies the maximum percentage of low-quality bases allowed. V2 specifies the minimum base quality. Any base with quality less than V2 is considered a low-quality base. Any sequence containing a percentage of low-quality bases greater than V1 is filtered out and not saved in the output file.[0 10]
'MeanQuality'Positive scalar that specifies the minimum threshold on the average base quality across each sequence. Any sequence with average base quality less than this value is filtered out.0
'MinLength'Nonnegative integer that specifies the minimum threshold on the sequence length allowed. Any sequence with length less than this value is filtered out. 1

Example: 'Method','MaxPercentLowQualityBases','Threshold',[10 20]

Size of the sliding window to apply the filtering criterion to a sequence, specified as a positive integer. The size of the window corresponds to the number of bases that the function uses at one time to apply the criterion. If any window fails the criterion, the whole sequence is discarded.

The default is Inf, that is, the filtering criterion is applied to the whole sequence.

Example: 'WindowSize',100

Base quality encoding format, specified as a character vector or string.

Example: 'Encoding','Sanger'

Relative or absolute path to the output file directory, specified as a character vector or string. The default is the current directory.

Example: 'OutputDir','F:\results'

Suffix to use in the output file name, specified as a character vector or string. It is inserted after the input file name and before the file extension. The default is '_filtered'.

Example: 'OutputSuffix','_WindowSize100_filtered'

Whether to consider the input files as pairs for paired-end sequence data, specified as true or false.

If true, the input files are read as pairs, and the sequence data is maintained in sync between the files. That is, if a sequence is filtered out in the first file, the corresponding sequence in the paired file is also filtered out.

Example: 'PairedFiles',true

Whether to save singleton sequences in a separate output file, specified as true or false. To set this to true, the 'PairedFiles' option must also be set to true.

A singleton sequence is the sequence that pass the filtering criterion but its corresponding sequence in the paired file does not. If true, singleton sequences are saved in a separate file with the suffix '_singleton'. The default is false, meaning that, only sequences that pass the filtering criterion in both input files of a given pair are saved in the output files.

Example: 'PairedFiles',true,'WriteSingleton',true

Boolean indicating whether to perform computation in parallel, specified as true or false.

For parallel computing, you must have Parallel Computing Toolbox™. If a parallel pool does not exist, one is created automatically when the auto-creation option is enabled in your parallel preferences. Otherwise, computation runs in serial mode.

Note

There is a cost associated with sharing large input files across workers in a distributed environment. In some cases, running in parallel may not be beneficial in terms of performance.

Example: 'UseParallel',true

Output Arguments

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Output file names, returned as a cell array of character vectors.

Number of sequences selected from each input file, returned as a scalar or an n-by-1 vector where n is the number of input files. If there are multiple input files, the order within nSeqIn corresponds to the order of the input files.

Number of sequences excluded from each input file, returned as a scalar or an n-by-1 vector where n is the number of input files. If there are multiple input files, the order within nSeqOut corresponds to the order of the input files.

Extended Capabilities

See Also

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Introduced in R2016b

Bioinformatics Toolbox Documentation

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