Call variants
1.0
Call variants tool
Call variants for a reference sequence with assembly
Uses SAMTools mpileup, bcftools and vcfutils
snp
Input sequence
Input reference sequence
Sequence
Nucleic
Input assembly
Input assembly (sorted BAM)
Text
Output variations
Output variations
Text
'*.snp'
Max number of reads per input BAM
At a position, read maximally the number of reads per input BAM. (mpileup)(-d)
Integer
Minimum mapping quality
Minimum mapping quality for an alignment to be used. (mpileup)(-q)
Integer
Min sample fraction
Skip loci where the fraction of samples covered by reads is below FLOAT. (bcf view)(-d)
Float
Min read depth
Minimum read depth. (varFilter) (-d)
Integer
Max read depth
Maximum read depth. (varFilter) (-D)
Integer