Hello Everyone,
I am currently analysing GBS data using stacks software as i ma currently facing some problem with ref_map.pl.
According to this script not getting proper output for this run.
this is the log file information form ref_map.pl
I am currently analysing GBS data using stacks software as i ma currently facing some problem with ref_map.pl.
According to this script not getting proper output for this run.
HTML Code:
ref_map.pl version 1.37 started at 2016-04-29 16:52:29
/usr/local/bin/ref_map.pl -T 4 -m 3 -n 1 -b 2 -o ref_out/ -S -s RG-1.bam
Identifying unique stacks; file 1 of 1 [RG-1]
/usr/local/bin/pstacks -t bam -f RG-1.bam -o ref_out -i 1 -p 4 -m 3 2>&1
Min depth of coverage to report a stack: 3
Model type: SNP
Alpha significance level for model: 0.05
BAM support was not enabled when Stacks was compiled.
Parsing RG-1.bam
Analyzed 0 sequence reads; Identified 0 unique stacks from those reads.
Merged 0 unique Stacks into 0 loci.
Identifying polymorphic sites and calling consensus sequences...done.
Number of utilized reads 0
Mean coverage depth is -nan; Std Dev: -0; Max: 0
Writing loci, SNPs, alleles to 'ref_out/...'
Wrote 0 loci, excluded 0 loci due to insuffient depth of coverage; blacklisted 0 loci.
/usr/local/bin/cstacks -g -b 2 -o ref_out -s ref_out/RG-1 -p 4 -n 1 2>&1
Number of mismatches allowed between stacks: 1
Loci matched based on genomic location.
Constructing catalog from 1 samples.
Initializing new catalog...
Parsing ref_out/RG-1.tags.tsv.gz
Parsing ref_out/RG-1.snps.tsv.gz
Parsing ref_out/RG-1.alleles.tsv.gz
Building an index of the catalog.
Writing catalog to 'ref_out/... done.
/usr/local/bin/sstacks -g -b 2 -c ref_out/batch_2 -o ref_out -s ref_out/RG-1 -p 4 2>&1
Searching for matches by genomic location...
Parsing ref_out/batch_2.catalog.tags.tsv.gz
Parsing ref_out/batch_2.catalog.snps.tsv.gz
Parsing ref_out/batch_2.catalog.alleles.tsv.gz
Processing sample 'ref_out/RG-1' [1 of 1]
Parsing ref_out/RG-1.tags.tsv.gz
Parsing ref_out/RG-1.snps.tsv.gz
Parsing ref_out/RG-1.alleles.tsv.gz
/usr/local/bin/populations -b 2 -P ref_out -s -t 4 2>&1
A population map was not specified, all samples will be read from 'ref_out/' as a single popultaion.
Fst kernel smoothing: off
Bootstrap resampling: off
Percent samples limit per population: 0
Locus Population limit: 1
Minimum stack depth: 0
Log liklihood filtering: off; threshold: 0
Minor allele frequency cutoff: 0
Maximum observed heterozygosity cutoff: 1
Applying Fst correction: none.
No population map specified, building file list.
Found 2 input file(s).
1 population found
1: RG-1, RG-1.sorted
1 group of populations found
1: 1
Parsing ref_out/batch_2.catalog.tags.tsv.gz
Parsing ref_out/batch_2.catalog.snps.tsv.gz
Parsing ref_out/batch_2.catalog.alleles.tsv.gz
Catalog is not reference aligned, arbitrarily ordering catalog loci.
Unable to open 'ref_out/RG-1'
Warning: unable to find any matches in file 'RG-1', excluding this sample from population analysis.
Unable to open 'ref_out/RG-1.sorted'
Warning: unable to find any matches in file 'RG-1.sorted', excluding this sample from population analysis.
Populating observed haplotypes for 0 samples, 0 loci.
Writing SQL markers file to 'ref_out/batch_2.markers.tsv'
Removing 0 loci that did not pass sample/population constraints... retained 0 loci.
refmap_map.pl completed at 2016-04-29 16:52:29
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