Modify a set of reference sequences using a set of variants


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Documentation for package ‘transmogR’ version 1.5.1

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cleanVariants Check provided variants for compatibility
cleanVariants-method Check provided variants for compatibility
cleanVariants-methods Check provided variants for compatibility
digestSalmon Parse the output from salmon
genomogrify Mogrify a genome using a set of variants
genomogrify-method Mogrify a genome using a set of variants
genomogrify-methods Mogrify a genome using a set of variants
indelcator Substitute InDels into one or more sequences
indelcator-method Substitute InDels into one or more sequences
overlapsByVar Count overlaps by variant type
overlapsByVar-method Count overlaps by variant type
overlapsByVar-methods Count overlaps by variant type
owl OverWrite Letters in an XStringSet
owl-method OverWrite Letters in an XStringSet
parY Get the PAR-Y Regions From a Seqinfo Object
parY-method Get the PAR-Y Regions From a Seqinfo Object
parY-methods Get the PAR-Y Regions From a Seqinfo Object
shiftByVar Calculate new exon co-ordinates
sjFromExons Obtain Splice-Junctions from Exons and Transcripts
transmogrify Mogrify a transcriptome using a set of variants
transmogrify-method Mogrify a transcriptome using a set of variants
transmogrify-methods Mogrify a transcriptome using a set of variants
upsetVarByCol Show Variants by Impacted Columns
varTags Create a set of tags indicating overlap status with variants
varTypes Identify SNVs, Insertions and Deletions