Man page - sga-astat(1)
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Manual
SGA-ASTAT
NAMESYNOPSIS
DESCRIPTION
OPTIONS
AUTHOR
NAME
sga-astat - Compute Myersโ a-statistic for a set of contigs using the read alignments in in.bam
SYNOPSIS
sga-astat [options] <in.bam>
DESCRIPTION
The major goal of SGA is to be very memory efficient, which is achieved by using a compressed representation of DNA sequence reads.
SGA is a de novo assembler for DNA sequence reads. It is based on Gene Myersโ string graph formulation of assembly and uses the FM-index/Burrows-Wheeler transform to efficiently find overlaps between sequence reads.
OPTIONS
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-m=INT |
only compute a-stat for contigs at least INT bases in length |
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-b=INT |
use the longest INT contigs to perform the initial estimate of the arrival rate (default: 20) |
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-n=INT |
perform INT bootstrap iterations of the estimate |
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-g=INT |
use INT as the genome size instead of estimating it |
--no-duplicates
do not use duplicate reads to calculate statistics
AUTHOR
This manpage was written by Andreas Tille for the Debian distribution and can be used for any other usage of the program.