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Releases
tugbadogan edited this page Jan 28, 2016
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- Minor bug in CW counting is fixed.
- SAM files can now separately be read into *.depth files, and then merged.
- New -nsam parameter to read specific SAM files in the READ mode.
- New CONC mode (--conc) to concatenate/merge different *.depth files using the new -concdepth parameter. These different files may be from different library preparations (see below).
- Multiple library support added.
- Several bug fixes.
- Bugs in non-autosomal chromosome processing for male samples are fixed.
- Pseudoautosomal support added through -pseudoa paramater. You can enter the pseudoautosomal regions in BED format in the PREP mode. This is optional; but the configuration file generated and used by this version is not compatible with the previous versions. You need to recreate the configuration file using the PREP mode.
- Code cleanup to facilitate easier addition of new features.
- SAM headers are now ignored.
- Segmentation fault with some kernels & gcc due to an unallocated string is fixed.
- Compilation errors in MacOSX are fixed.
- Compilation error in x86_64 systems with gcc version > 4.33 is fixed.
- Minor bug in parsing chromosome names that end with whitespace is fixed.
- Bug causing infinite loop in control region selection is fixed..
- Bug in GC normalization is fixed.
- Bug in CN estimation in chrX and chrY for male mammals is fixed.
- GC counting bug in LW when an assembly gap is 1 character is fixed.
- Bug causing segmentation fault when CW_SIZE is set to a small value is fixed.
- A bug in GC normalization is fixed.
- Initial release of mrCaNaVaR.
- This version only predicts absolute copy numbers. CNV interval output will be included in the next release. For the time being, you can select intervals with increased copy number (i.e. > 2.5) and merge such intervals using BEDtools.