Man page - fastaq-to_tiling_bam(1)
Packages contains this manual
- fastaq-filter(1)
- fastaq-version(1)
- fastaq-fasta_to_fastq(1)
- fastaq-split_by_base_count(1)
- fastaq-to_fasta(1)
- fastaq-translate(1)
- fastaq-reverse_complement(1)
- fastaq-add_indels(1)
- fastaq-to_tiling_bam(1)
- fastaq-acgtn_only(1)
- fastaq-trim_ends(1)
- fastaq-to_orfs_gff(1)
- fastaq-get_ids(1)
- fastaq-to_perfect_reads(1)
- fastaq-trim_contigs(1)
- fastaq-scaffolds_to_contigs(1)
- fastaq-search_for_seq(1)
- fastaq-to_mira_xml(1)
- fastaq-to_random_subset(1)
- fastaq-to_fake_qual(1)
- fastaq-sort_by_size(1)
- fastaq-merge(1)
- fastaq-enumerate_names(1)
- fastaq-strip_illumina_suffix(1)
- fastaq-to_boulderio(1)
- fastaq-caf_to_fastq(1)
- fastaq-count_sequences(1)
- fastaq-interleave(1)
- fastaq-make_random_contigs(1)
- fastaq-to_unique_by_id(1)
- fastaq-deinterleave(1)
- fastaq-replace_bases(1)
- fastaq-capillary_to_pairs(1)
- fastaq-sequence_trim(1)
- fastaq-sort_by_name(1)
- fastaq-expand_nucleotides(1)
- fastaq-chunker(1)
- fastaq-get_seq_flanking_gaps(1)
- fastaq(1)
apt-get install fastaq
Manual
FASTAQ-TO_TILING_BAM
NAMEDESCRIPTION
positional arguments:
options:
NAME
fastaq_to_tiling_bam - Make a BAM file of reads uniformly spread across the input reference
DESCRIPTION
usage: fastaq_to_tiling_bam [options] <infile> <read_length> <read_step> <read_prefix> <outfile>
Takes a sequence file. Makes a BAM file containing perfect (unpaired) reads tiling the whole genome
positional arguments:
|
infile |
Name of input fasta/q file |
read_length
Length of reads
read_step
Distance between start of each read
read_prefix
Prefix of read names
outfile
Name of output BAM file
options:
-h , --help
show this help message and exit
--qual_char QUAL_CHAR
Character to use for quality score [I]
--read_group READ_GROUP
Add the given read group ID to all reads [42]
Important: assumes that samtools is in your path