nanook(1)
flexible, multi-reference software for pre- and post-alignment analysis of nanopore sequencing data, quality and error
Description
NANOOK
NAME
nanook - flexible, multi-reference software for pre- and post-alignment analysis of nanopore sequencing data, quality and error profiles
SYNOPSIS
nanook <extract|align|analyse|compare|process> [options]
DESCRIPTION
NanoOK
(pronounced na-nook) is a tool for extraction, alignment and
analysis of Nanopore reads. NanoOK will extract reads as
FASTA or FASTQ
files, align them (with a choice of alignment tools), then
generate a
comprehensive multi-page PDF report containing yield,
accuracy and
quality analysis. Along the way, it generates plain text
files which can
be used for further analysis, as well as graphs suitable for
inclusion
in presentations and papers.
OPTIONS
extract options:
|
-s|-sample <dir> specifies sample directory |
||
|
-f|-reads specifies alternative dir for FAST5 files (default fast5) |
Can be absolute (beginning with /) or relative e.g. -f reads/downloads if replicating Metrichor file structure
|
-a|-fasta specifies FASTA file extraction (default) | |
|
-q|-fastq specifies FASTQ file extraction | |
|
-basecallindex specifies the index of the analysis (default: latest) | |
|
-mergereads to generate merged FASTA files in addition to single read files | |
|
-minquality <value> to set the minimum quality for a ’pass’ read |
|
-l|-samplelist <file> specifies a sample list file |
||
|
-o|-outputdir <directory> specifies an output directory |
||
|
-type <2d|template|complement> specifies an output directory |
|
-process <file> specifies a process file |
Valid aligners: last, bwa, blasr, marginalign, graphmap
AUTHOR
This manpage was written by Andreas Tille for the Debian distribution and can be used for any other usage of the program.