File Changes for angie
switch to commits view, user indexv255_base to v256_preview (2011-08-08 to 2011-08-16) v256
- src/hg/hgTables/hgTables.c
- lines changed 2, context: html, text, full: html, text
Bug #454 (hgTables fills the error logs with no-content errors):Removing an old debugging printf that must have been accidentally committed.
- src/hg/hgTracks/vcfTrack.c
- lines changed 71, context: html, text, full: html, text
Feature #2823 (VCF track handler): Added UI control over height of haplotype-sorting display.
- lines changed 34, context: html, text, full: html, text
Feature #2821 (VCF parser): improved representation of alleles:parse ref and comma-sep'd alt allele string into count and array
inside record, so callers don't all have to parse the comma-sep'd
alternate allele string.
- lines changed 8, context: html, text, full: html, text
Feature #3710 (vcfTabix UI options): added checkbox to enable/disable haplotype sorting display.
- lines changed 28, context: html, text, full: html, text
Feature #3710 (vcfTabix UI options): added option to use pgSnp colors instead of blueRef/redAlt in haplotype sorting display.
- lines changed 165, context: html, text, full: html, text
Feature #3711 (vcfTabix haplotype sorting display): Draw hierarchical tree in left label area (as much as can fit there).
- lines changed 16, context: html, text, full: html, text
Feature #3711 (vcfTabix haplotype-sorting display): Limit the numberof variants close to the center variant that we use for clustering,
to prevent the clustering from timing out in large regions with large
genotype counts (e.g. 1094 genotypes from 1000 Genomes phase 1 interim).
- src/hg/hgc/hgc.c
- lines changed 1, context: html, text, full: html, text
MLQ #4908 (genomicSuperDups strand): genomicSuperDups' strand column isalready displayed in hgc output as "Other Position Relative Orientation"
which is its real meaning (not the usual sense of the strand column).
So don't tell bedPrintPos that we have bed 6, because then it prints out
a confusing redundant "Strand:".
- src/hg/hgc/vcfClick.c
- lines changed 39, context: html, text, full: html, text
Feature #2823 (VCF track handler): Added summaries of genotype and allele freqs to details page.
- lines changed 53, context: html, text, full: html, text
Feature #2821 (VCF parser): improved representation of alleles:parse ref and comma-sep'd alt allele string into count and array
inside record, so callers don't all have to parse the comma-sep'd
alternate allele string.
- src/hg/inc/vcfUi.h
- lines changed 4, context: html, text, full: html, text
Feature #2823 (VCF track handler): Added UI control over height of haplotype-sorting display.
- lines changed 3, context: html, text, full: html, text
Feature #3710 (vcfTabix UI options): added checkbox to enable/disable haplotype sorting display.
- lines changed 4, context: html, text, full: html, text
Feature #3710 (vcfTabix UI options): added option to use pgSnp colors instead of blueRef/redAlt in haplotype sorting display.
- src/hg/lib/pgSnp.c
- lines changed 92, context: html, text, full: html, text
Feature #2821 (VCF parser): improved representation of alleles:parse ref and comma-sep'd alt allele string into count and array
inside record, so callers don't all have to parse the comma-sep'd
alternate allele string.
- lines changed 18, context: html, text, full: html, text
Feature #3710 (vcfTabix UI options): added checkbox to enable/disable haplotype sorting display.
- src/hg/lib/vcfUi.c
- lines changed 25, context: html, text, full: html, text
Feature #2823 (VCF track handler): Added UI control over height of haplotype-sorting display.
- lines changed 33, context: html, text, full: html, text
Feature #3710 (vcfTabix UI options): added checkbox to enable/disable haplotype sorting display.
- lines changed 37, context: html, text, full: html, text
Feature #3710 (vcfTabix UI options): added option to use pgSnp colors instead of blueRef/redAlt in haplotype sorting display.
- src/inc/vcf.h
- lines changed 2, context: html, text, full: html, text
Feature #2821 (VCF parser): improved representation of alleles:parse ref and comma-sep'd alt allele string into count and array
inside record, so callers don't all have to parse the comma-sep'd
alternate allele string.
- src/lib/tests/vcfParseTest.c
- lines changed 1, context: html, text, full: html, text
Feature #2821 (VCF parser): improved representation of alleles:parse ref and comma-sep'd alt allele string into count and array
inside record, so callers don't all have to parse the comma-sep'd
alternate allele string.
- src/lib/vcf.c
- lines changed 22, context: html, text, full: html, text
Feature #2821 (VCF parser): improved representation of alleles:parse ref and comma-sep'd alt allele string into count and array
inside record, so callers don't all have to parse the comma-sep'd
alternate allele string.
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