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Description:

From a FASTA file and a matching QUAL file, generates a FASTQ file. A minimal FASTQ file omits the redundant sequence label on the quality scores; the quality scores for a sequence are assumed to follow immediately after the sequence with which they are associated. The output FASTQ file will be generated in the specified output directory with the same name as the input FASTA file, suffixed with ‘.fastq’. A FASTQ file will be split into FASTA and QUAL files, and generated in the designated output directory.

Usage: convert_fastaqual_fastq.py [options]

Input Arguments:

Note

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[REQUIRED]

-f, --fasta_file_path
Input FASTA or FASTQ file.

[OPTIONAL]

-q, --qual_file_path
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-o, --output_dir
Handheld Strap Gold Sizes Evening Fabric Sparkling Bridal with Glitter in Small Chain Ladies For Xardi Sequins Medium Clutch Women Bags Detachable Light London Output directory. Will be created if does not exist. [default: .]
-c, --conversion_type
Clutch Chain Sizes Bags London For Evening Gold Small Strap Fabric Detachable Handheld Bridal Sequins Light Ladies Medium Xardi Women Sparkling Glitter in with Type of conversion: fastaqual_to_fastq or fastq_to_fastaqual [default: fastaqual_to_fastq]
-a, --ascii_increment
The number to add (subtract if coverting from FASTQ) to the quality score to get the ASCII character (or numeric quality score). [default: 33]
-F, --full_fasta_headers
Include full FASTA headers in output file(s) (as opposed to merely the sequence label). [default: False]
-b, --full_fastq
Include identifiers on quality lines in the FASTQ file (those beginning with a “+”). Irrelevant when converting from FASTQ. [default=False]
-m, Fabric Xardi Strap Clutch with Evening Detachable Sparkling Chain Glitter Bridal Bags Ladies Handheld For Women Gold in Medium London Sizes Sequins Light Small --multiple_output_files
Create multiple FASTQ files, one for each sample, or create multiple matching FASTA/QUAL for each sample. [default=False]

Output:

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Outputs a complete or minimal FASTQ file, which omits the redundant sequence label on the quality scores, or splits FASTQ file into matching FASTA/QUAL files.

Example:

Using the input files seqs.fna and seqs.qual, generate seqs.fastq in the fastq_files directory:

convert_fastaqual_fastq.py -f seqs.fna -q seqs.qual -o fastq_files/
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Example:

Using input seqs.fastq generate fasta and qual files in fastaqual directory:

convert_fastaqual_fastq.py -c fastq_to_fastaqual -f seqs.fastq -o fastaqual

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