Changes in version 1.4.2 ------------------------- SIGNIFICANT USER-VISIBLE CHANGES o loadCNVcalls() does not check cnvs.file names by default when loading (read.csv()) the cnvs.file o loadCNVcalls() allows optional check.names.cnvs.file parameter o Vignette updated MINOR o Added rmarkdown to Suggets in DESCRIPTION file Changes in version 1.4.1 ------------------------- BUG FIXES o Bug fixed: SNVs were not being correctly loaded after last Bioconductor update SIGNIFICANT USER-VISIBLE CHANGES o plotAllCNVs() allows 'genome' parameter to work with different genomes MINOR o Minor vignette fixes o Other minor fixes Changes in version 1.1.6 ------------------------- SIGNIFICANT USER-VISIBLE CHANGES o plotVariantsForCNV() allows multiple visual adjustements MINOR o Added error control in loadVCFs(): heterozygous.range and homozygous.range cannot overlap Changes in version 1.1.5 ------------------------- SIGNIFICANT USER-VISIBLE CHANGES o Added ignore.unexpected.rows parameter to loadCNVcalls() function to ignore CNV calls which deletion/duplication value is not the expected one. BUG FIXES o Some SNV callers can produce calls with a genotype indicating that the variant actually was not found. Variants with GTs like "0/0 ./. 1/0" are now discarded. o Certain SNV callers can produce SNV calls with more than two alt values (multiple alt alleles). These variants are now discarded. Changes in version 1.1.4 ------------------------- SIGNIFICANT USER-VISIBLE CHANGES o Improved CNVfilteR accuracy. margin.pct parameter was added to filterCNVs() and ht.deletions.threshold default value was modified to 30. o Loading variants process optimized (multiple times faster) o filterCNVs() function optimized o min.total.depth default value modified to 10 o Added multiple modifications to the vignette BUG FIXES o Fixed bug when plotting a CNV with no SNV variants falling in it Changes in version 1.1.3 ------------------------- BUG FIXES o Fixed bug when processing variants in the limits of heterozygous.range and heterozygous.range Changes in version 1.1.2 ------------------------- SIGNIFICANT USER-VISIBLE CHANGES o Added sample.name parameter to loadCNVcalls() function to allow explicitly setting sample name o deletion and duplication parameters can be vectors in loadCNVcalls() function, so multiple values are allowed BUG FIXES o Fixed bug happening in loadSNPsFromVCF() when ref and alt support was 0 o Fixed bug when processing list.support.field in loadSNPsFromVCF() o Added error control when allele frequency is not numeric o Minor fixes