Fasta

availeble from version 0.559+

This option creates a fasta file from a sequencing data file (bam file). The function uses genome information in the bam header to determine the length and chromosome names. For the sites without data an "N" is written.

<classdiagram type="dir:LR">

[One bam file{bg:orange}]->[sequencing data|random base (-doFasta 1);consensus base (-doFasta 2)]

[sequencing data]->doFasta[fasta file{bg:blue}]

</classdiagram>

Brief Overview

> ./angsd -doFasta
--------------
analysisFasta.cpp:
	-doFasta	0
	1: use a random base
	2: use the most common base (needs -doCounts 1)
	-minQ		13	(remove bases with qscore<minQ)

options

-doFasta 1

sample a random base at each position

-doFasta 2

use the most common base. In the case of ties a random base is chosen among the bases with the same maximum counts. The "-doCounts 1" options for allele counts is needed in order to determine the most common base

-minQ [INT]

minimum base quality score

Example

Create a fasta file bases from a random samples of bases

./angsd -i smallNA07056.mapped.ILLUMINA.bwa.CEU.low_coverage.20111114.bam -doFasta 1