Update docs of FastaAlternateReferenceMaker as promised in older GS thread
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@ -47,7 +47,8 @@ import java.util.List;
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* <p>
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* Given variant tracks, it replaces the reference bases at variation sites with the bases supplied by the ROD(s).
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* Additionally, allows for one or more "snpmask" VCFs to set overlapping bases to 'N'.
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* Note that if there are multiple variants at a site, it takes the first one seen.
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* Note that if there are multiple variants at a site, it chooses one of them randomly.
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* Also note that this tool works only for SNPs and for simple indels (but not for things like complex substitutions).
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* Reference bases for each interval will be output as a separate fasta sequence (named numerically in order).
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*
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* <h2>Input</h2>
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