deepSNV -- an R package for subclonal variant calling.

Changes in version 1.2.3 (2012-04-10)
Bugfixes
* Fixed Vignette
* Jumped a few numbers due to automated bioc version numbering

Changes in version 1.0.0 (2012-03-29)
Updates
* Added CITATION file
* Made NEWS (this file) R-readable
* Changed Vignette

Changes in version 0.99.3
Bugfixes
* Fixed error in summary() when there were no significant SNVs.
* Some fixes if only a single column of the alignment is selected

Changes in version 0.99.2 (2012-01-20)
Updates
* Changed plot to S3 method (to avoid warning in R-devel)

Changes in version 0.99.1 (2012-01-06)
Updates
* Added small .bam example files test.bam, control.bam with 100 positions.
* Modified man pages for bam2R()
* Modified man page for coordinates()
* Corrected example of consensusSequence()
* Compressed .RData files with tools::resaveRdaFiles
* Changed vignette to attach data, rather than load remotely.
* Argument "regions" of deepSNV can be a GRanges object.

Changes in version 0.99.0 (2011-12-21)
Updates
* Added BiocViews field
* Added HIVmix data
* Added new examples
* Registered bam2R with R_registerRoutines
* New accessor functions "test", "control", "p.val", and "coordinates"
* Updated vignette


Changes in version 0.9.5
Updates
* "summary" now reports additional columns from regions slot.
Bugfixes 
* drop=FALSE in subsetting and summary.

Changes in version 0.9.4
Updates
* Directly link to static samtools library provided by Rsamtools
* Load example .bam files over http

Changes in version 0.9.3
* Added beta-binomial model
* Extended documentation
* Use summary instead of significantSNV

Changes in version 0.9.2
* Minor bugfixes

Changes in version 0.9.1
Minor bugfixes

Changes in version 0.9.0
Pre-release