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'''glfSingle''' is a [[GLF]]-based variant caller for next-generation sequencing data. It takes a [[GLF]] format genotype likelihood file as input and generates a [[VCF]]-format set of variant calls as output.
== Basic Usage Example ==
Here is an example of how <code>glfSingle</code> works:
glfSingle -g NA19240.chrom20.SLX.glf -b NA19240.chrom20.SLX.vcf > NA19240.chrom20.SLX.log
== Command Line Options ==
== Model for Variant Calling ==
== Basic Usage Example ==
Here is an example of how <code>glfSingle</code> works:
glfSingle -g NA19240.chrom20.SLX.glf -b NA19240.chrom20.SLX.vcf > NA19240.chrom20.SLX.log
== Command Line Options ==
== Model for Variant Calling ==
