filter-illumina-index 1.0.dev1

Filter a Illumina FASTQ file based on index sequence

filter_illumina_index

Filter a Illumina FASTQ file based on index sequence.

Reads a Illumina FASTQ file and compares the sequence index in the sample number position of the sequence identifier to a supplied sequence index. Entries that match the sequence index are filtered into the 'filtered' file (if any) and entries that don't match are filtered into the 'unfiltered' file (if any). Displays the count of total, filtered and unfiltered reads. Matching with mismatches, and input and output gzip compression are supported.

For information on Illumina sequence identifiers in FASTQ files, see: http://support.illumina.com/content/dam/illumina-support/help/BaseSpaceHelp_v2/Content/Vault/Informatics/Sequencing_Analysis/BS/swSEQ_mBS_FASTQFiles.htm

Usage details

usage: filter_illumina_index [-h] [--version] [-f FILTERED] [-u UNFILTERED] -i
                             INDEX [-m MISMATCHES] [-c] [-v]
                             inputfile

positional arguments:
  inputfile             Input FASTQ file, compression supported

optional arguments:
  -h, --help            show this help message and exit
  --version             show program's version number and exit
  -f FILTERED, --filtered FILTERED
                        Output FASTQ file containing filtered (positive) reads
                        (default: None)
  -u UNFILTERED, --unfiltered UNFILTERED
                        Output FASTQ file containing unfiltered (negative)
                        reads (default: None)
  -m MISMATCHES, --mismatches MISMATCHES
                        Maximum number of mismatches to accept (default: 0)
  -c, --compressed      Compress output files (note: file extension not
                        modified) (default: False)
  -v, --verbose         Show verbose output (default: False)

required named arguments:
  -i INDEX, --index INDEX
                        Sequence index to filter for (default: None)

Example usage

filter_illumina_index srv\example_reads.fastq --index GATCGTGT --filtered var\filtered_reads.fastq --unfiltered var\unfiltered_reads.fastq

This will process srv\example_reads.fastq, matching to index GATCGTGT with no mismatches allowed (default). Reads matching this index will be saved to var\filtered_reads.fastq and those not matching this index will be saved to var\unfiltered_reads.fastq. In addition, the following output will be displayed:

Total reads: 30
Filtered reads: 29
Unfiltered reads: 1

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Additional details

• Author: Tet Woo Lee
• Copyright: © 2018 Tet Woo Lee
• Licence: GPLv3
• Dependencies: Biopython, tested on v1.72

Change log

version 1.0.dev1 2018-12-13 : First working version