X-Git-Url: http://woldlab.caltech.edu/gitweb/?p=samtools.git;a=blobdiff_plain;f=NEWS;h=de556796b15685ede8723e928f0d8838a9098ada;hp=946ba7b4e98d584081b846105bde5f438f6e3ba1;hb=e42445c748ed193f8d0a4277a844fa848f30c132;hpb=fa217aa47313e2535cbd2d4bb034cfd405162662 diff --git a/NEWS b/NEWS index 946ba7b..de55679 100644 --- a/NEWS +++ b/NEWS @@ -1,4 +1,37 @@ -Beta release 0.1.14 (16 March, 2011) +Beta Release 0.1.15 (10 April, 2011) +~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ + +Noteable changes: + + * Allow to perform variant calling or to extract information in multiple + regions specified by a BED file (`samtools mpileup -l', `samtools view -L' + and `bcftools view -l'). + + * Added the `depth' command to samtools to compute the per-base depth with a + simpler interface. File `bam2depth.c', which implements this command, is the + recommended example on how to use the mpileup APIs. + + * Estimate genotype frequencies with ML; perform chi^2 based Hardy-Weinberg + test using this estimate. + + * For `samtools view', when `-R' is specified, drop read groups in the header + that are not contained in the specified file. + + * For `samtools flagstat', separate QC-pass and QC-fail reads. + + * Improved the command line help of `samtools mpileup' and `bcftools view'. + + * Use a global variable to control the verbose level of samtools stderr + output. Nonetheless, it has not been full utilized. + + * Fixed an issue in association test which may report false associations, + possibly due to floating point underflow. + +(0.1.15: 10 April 2011, r949:203) + + + +Beta release 0.1.14 (21 March, 2011) ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ This release implements a method for testing associations for case-control @@ -9,17 +42,41 @@ has not been evaluated on real data. Another new feature is to make X chromosome variant calls when female and male samples are both present. The user needs to provide a file indicating the -ploidy of each sample. +ploidy of each sample (see also manual bcftools/bcftools.1). + +Other notable changes: + + * Added `bcftools view -F' to parse BCF files generated by samtools r921 or + older which encodes PL in a different way. -Other new features: + * Changed the behavior of `bcftools view -s'. Now when a list of samples is + provided, the samples in the output will be reordered to match the ordering + in the sample list. This change is mainly designed for association test. + + * Sped up `bcftools view -v' for target sequencing given thousands of samples. + Also added a new option `view -d' to skip loci where only a few samples are + covered by reads. + + * Dropped HWE test. This feature has never been implemented properly. An EM + should be much better. To be implemented in future. + + * Added the `cat' command to samtools. This command concatenate BAMs with + identical sequence dictionaries in an efficient way. Modified from bam_cat.c + written by Chris Saunders. + + * Added `samtools view -1' to write BAMs at a low compression level but twice + faster to create. The `sort' command generates temporary files at a low + compression level as well. + + * Added `samtools mpileup -6' to accept "BAM" with Illumina 1.3+ quality + strings (strictly speaking, such a file is not BAM). * Added `samtools mpileup -L' to skip INDEL calling in regions with excessively high coverage. Such regions dramatically slow down mpileup. - * Added `bcftools view -F' to parse BCF files generated by samtools r921 or - older which encode PL in a different way. + * Updated `misc/export2sam.pl', provided by Chris Saunders from Illumina Inc. -(0.1.14: 16 March 2011, r930:163) +(0.1.14: 21 March 2011, r933:170)