-
Notifications
You must be signed in to change notification settings - Fork 8
fasta_data.sh
Usage:
fastq_data.sh <fastq_file>
Where <fastq_file> is a fastq file to be analyzed
This script takes a fastq file as input and produces a pdf file containing a brief summary of the data and accompanying plots which can be used to assess sequence quality. This is achieved using the seqTools package in R.
Input fastq file must have .fq or .fastq extension.
Output will be named:
fastq_data_results-<fastq_file>.pdf
Example:
fastq_data.sh read1.fastq
Output:
fastq_data_results-read1.fastq.pdf
This script requires that seqTools library be available in your R installation.
Script wiki pages:
akutils
akutils align_and_tree
akutils check
akutils check_result
akutils configure
akutils core diversity
akutils format_database
akutils join_paired_reads
akutils phix_filtering
akutils pick_otus
akutils primer_file
akutils primer_list
akutils print_config
akutils strip_primers
akutils test
akutils test_result
akutils update
ancomR.sh
biom-summarize_folder.sh
biomtotxt.sh
concatenate_fastqs.sh
convert_table_for_ancomR.sh
fastq_data.sh
fasta_length_histogram.sh
fastq_length_histogram.sh
filter_fasta_by_length.sh
filter_fastq_by_length.sh
filter_observations_by_sample.sh
indicator_species.sh
ITSx_parallel.sh
mapcats.sh
preprocess_otus_for_ghost-tree.sh
slurm_builder.sh
synthetic_index.sh
two-way_permanova.sh
txttobiom.sh
unwrap_fasta.sh
Tutorial pages:
akutils tutorial
ITS analysis
slurm usage
Running akutils on monsoon
Example: 2x300, 2 loci
akutils wiki home:
akutils wiki home
akutils home page:
akutils home page
akutils github page:
akutils github page