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Small fast cprogram to extract bases from a fasta file. Download here [http://popgen.dk/software/download/refFinder/refFinder.tar.gz] | Small fast cprogram to extract bases from a fasta file. Download here [http://popgen.dk/software/download/refFinder/refFinder.tar.gz] | ||
=Install= | |||
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=Example= | =Example= |
Revision as of 16:04, 12 March 2014
Small fast cprogram to extract bases from a fasta file. Download here [1]
Install
Example
Generate samtools chr pos ref doing
samtools mpileup -b smallBam.filelist -f /space/genomes/refgenomes/hg19/merged/hg19NoChr.fa |cut -f1-3 >small.sam
Use refFinder to find the bases for each position in small.sam
cut -f1-2 ../angsd/test/small.sam |./refFinder /space/genomes/refgenomes/hg19/merged/hg19NoChr.fa full >tst cmp tst small.bam
possible options are
- inputIsZero
- full
These are flags, so examples are
cut -f1-2 ../angsd/test/small.sam |./refFinder /space/genomes/refgenomes/hg19/merged/hg19NoChr.fa |head a g c t a c t c g g
Or if we want the chr position also
cut -f1-2 ../angsd/test/small.sam |./refFinder /space/genomes/refgenomes/hg19/merged/hg19NoChr.fa full |head 1 13999902 a 1 13999903 g 1 13999904 c 1 13999905 t 1 13999906 a 1 13999907 c 1 13999908 t 1 13999909 c 1 13999910 g 1 13999911 g
Or if the positions are zero index as opposed to one indexed:
cut -f1-2 ../angsd/test/small.sam |./refFinder /space/genomes/refgenomes/hg19/merged/hg19NoChr.fa full inputIsZero |head 1 13999902 g 1 13999903 c 1 13999904 t 1 13999905 a 1 13999906 c 1 13999907 t 1 13999908 c 1 13999909 g 1 13999910 g 1 13999911 g