May 16, 2014
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fix seqinfo merging in variantSummary

Michael Lawrence authored on 16/05/2014 21:33:43
May 13, 2014
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update to new bam_tally with support for XS counting, which we now support via BamTallyParam@count_xs.

Michael Lawrence authored on 13/05/2014 02:04:05
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add internal function for getting transcripts on the TP53 genome

Michael Lawrence authored on 13/05/2014 02:02:31
May 5, 2014
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bam_tally has reworked memory management to avoid memory "leaks" that seem to happen on our cluster

Michael Lawrence authored on 05/05/2014 21:02:45
May 2, 2014
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re-add counting of unique read positions (convenient when dupes are not marked) and fix an uninitialized value (param.cycle_breaks) detected by valgrind

Michael Lawrence authored on 02/05/2014 12:51:58
April 30, 2014
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add support for the noncovered argument; tells bam_tally to report even those positions that have no coverage

Michael Lawrence authored on 30/04/2014 17:05:27
April 18, 2014
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resync with stuff moving from IRanges to S4Vectors

Herve Pages authored on 18/04/2014 15:04:25
April 14, 2014
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disable read length guessing; just expect the user to provide it when they need the statistics that depend on it

Michael Lawrence authored on 14/04/2014 19:50:15
April 4, 2014
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drop the unique read position counts; renamed count.pos/count.neg to count.plus/count.minus (way better names)

Michael Lawrence authored on 04/04/2014 13:36:22
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bring back the unique read position count, and mean/variance of read positions

Michael Lawrence authored on 04/04/2014 13:16:32
April 2, 2014
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update GSTRUCT (bam_tally); add include_soft_clip parameter for counting over soft clips of a given max length (more accurate allele frequency)

Michael Lawrence authored on 02/04/2014 22:03:40
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ensure that seqlevel ordering from genome is preserved in result

Michael Lawrence authored on 02/04/2014 21:12:52
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be robust to different seqlevel orderings when merging Seqinfo from GmapGenome and BamFile

Michael Lawrence authored on 02/04/2014 20:54:46
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cleanup gmap_build interface, add 'circular' support (automatically derived from BSgenome) and turn off chromosome sorting by default

Michael Lawrence authored on 02/04/2014 12:59:22
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tweak consistency checks to allow NA values (when variant_strand=0)

Michael Lawrence authored on 02/04/2014 12:58:36