2015
	
		
	
		     		
		            	
    				05 May 2015	
    			
	     	
new tools available in Galaxy        	
    		        		
We are pleased to announce new tool integrations for Variant analysis in our 	
Galaxy
 server:
section Freebayes
- FreeBayes (0.9.20) - bayesian genetic variant detector
 
- BamLeftAlign - indels in BAM datasets
 
 section Vcflib tool suite
-  VCFfixup: Count the allele frequencies across alleles present in each record in the VCF file
 
- VCFselectsamples: Select samples from a VCF dataset
 
- VCFhetHomAlleles: Count the number of heterozygotes and alleles, compute het/hom ratio
 
- VCFdistance: Calculate distance to the nearest variant
 
- VCFannotateGenotypes: Annotate genotypes in a VCF dataset using genotypes from another VCF dataset
 
- VCFcombine: Combine multiple VCF datasets
 
- VCFflatten: Removes multi-allelic sites by picking the most common alternate
 
- VCF-VCFintersect: Intersect two VCF datasets
 
- VcfAllelicPrimitives: Split alleleic primitives (gaps or mismatches) into multiple VCF lines
 
- VCFcheck: Verify that the reference allele matches the reference genome
 
- VCFrandomSample: Randomly sample sites from VCF dataset
 
- VCFgenotype-to-haplotype: Convert genotype-based phased alleles into haplotype alleles
 
- VCFgenotypes: Convert numerical representation of genotypes to allelic
 
- VCFaddinfo: Adds info fields from the second dataset which are not present in the first dataset
 
- VCFfilter: filter VCF data in a variety of attributes
 
- VCFannotate: Intersect VCF records with BED annotations
 
- VCFprimers: Extract flanking sequences for each VCF record
 
- VCFsort: Sort VCF dataset by coordinate
 
- VCF-BEDintersect: Intersect VCF and BED datasets
 
- VCFbreakCreateMulti: Break multiple alleles into multiple records, or combine overallpoing alleles into a single record
 
- VCFleftAlign: Left-align indels and complex variants in VCF dataset
 
- VCFtoTab-delimited: Convert VCF data into TAB-delimited format
 
- VCFcommonSamples: Output records belonging to samples common between two datasets
 
 
 For any questions or bug reports, please contact us at: 	
urgi-support@versailles.inra.fr
 
 Thank you for using URGI Galaxy: 	
https://urgi.versailles.inra.fr/galaxy2