Filter a Illumina FASTQ file based on index sequence
Project description
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 (-m
parameter), and gzip compression for input
(detected on the basis of file extension) and output (specified using -c
parameter) 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
The directory srv
contains example reads in FASTQ and compressed FASTQ format with index GATCGTGT
and one read with a mismatch.
To test, run:
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
Additional details
- Author: Tet Woo Lee
- Copyright: © 2018 Tet Woo Lee
- Licence: GPLv3
- Dependencies: Biopython, tested on v1.72
Change log
version 1.0 2018-12-14 : Minor updates for PyPi and conda packaging
version 1.0.dev1 2018-12-13 : First working version
Project details
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