URL: http://anntools.sourceforge.net/
Proper Citation: AnnTools (RRID:SCR_005170)
Description: Software tool for annotating single nucleotide substitutions (SNP/SNV), small insertions/deletions (indels), and copy number variations (CNV) calls generated from sequencing and microarray data. Only human genome build 37/hg19 can be annotated at this time.
Abbreviations: AnnTools
Resource Type: software resource
Keywords: single nucleotide substitution, snp, snv, indel, copy number variation, sequencing, microarray, linux, unix, mac osx, python, mysql, genome annotation, genome, annotation
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