shovill1
Assemble bacterial isolate genomes from illumina paired-end reads
Overview
SYNOPSIS
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De novo assembly pipeline for Illumina paired reads
USAGE
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shovill [options]
--outdirDIR--R1R1.fq.gz--R2R2.fq.gz
GENERAL
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--help -
This help
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--version -
Print version and exit
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--check -
Check dependencies are installed
INPUT
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--R1 XXX -
Read 1 FASTQ (default: '')
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--R2 XXX -
Read 2 FASTQ (default: '')
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--depth N -
Sub-sample
--R1/--R2 to this depth. Disable with--depth0 (default: 150)
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--gsize XXX -
Estimated genome size eg. 3.2M <blank=AUTODETECT> (default: '')
OUTPUT
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--outdir XXX -
Output folder (default: '')
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--force -
Force overwrite of existing output folder (default: OFF)
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--minlen N -
Minimum contig length <0=AUTO> (default: 0)
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--mincov n.nn -
Minimum contig coverage <0=AUTO> (default: 2)
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--namefmt XXX -
Format of contig FASTA IDs in 'printf' style (default: 'contig%05d')
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--keepfiles -
Keep intermediate files (default: OFF)
RESOURCES
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--tmpdir XXX -
Fast temporary directory (default: '')
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--cpus N -
Number of CPUs to use (0=ALL) (default: 8)
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--ram n.nn -
Try to keep RAM usage below this many GB (default: 7.54)
ASSEMBLER
--assembler XXX Assembler: velvet spades skesa megahit (default: 'spades')
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--opts XXX -
Extra assembler options in quotes eg. spades: '--sc' (default: '')
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--kmers XXX -
K-mers to use <blank=AUTO> (default: '')
MODULES
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--trim -
Enable adaptor trimming (default: OFF)
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--noreadcorr -
Disable read error correction (default: OFF)
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--nostitch -
Disable read stitching (default: OFF)
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--nocorr -
Disable post-assembly correction (default: OFF)
HOMEPAGE
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https://github.com/tseemann/shovill - Torsten Seemann