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hsinnan75 / MapCaller

MapCaller – An efficient and versatile approach for short-read alignment and variant detection in high-throughput sequenced genomes
MIT License
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Missing \n in VCF header #66

Open tseemann opened 3 years ago

tseemann commented 3 years ago

##ALT=<ID=NON_REF,Description="Represents any possible alternative allele at this location">##INFO=<ID=RC,Number=1,Type=Integer,Description="Number of reads with start coordinate at this position.">

##FORMAT=<ID=PL,Number=G,Type=Integer,Description="Normalized, Phred - scaled likelihoods for genotypes as defined in the VCF specification">##FORMAT=<ID=F1R2,Number=R,Type=Integer,Description="Count of reads in F1R2 pair orientation supporting each allele"> Missing newline

hsinnan75 commented 3 years ago

Thank you. I've corrected the two lines.