VAT

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VAT Main Page


Contents


Introduction

The Variant Annotation Tool (VAT) consists of a set of modules to annotate genetic variants including SNPs and indels. This software package also contains a program to aggregate SNP and indel variants at the gene level. Subsequently, an image is generated for each gene to visualize the functional impact of these variants. This information can then be viewed and shared using a web-interface. In addition to annotation of the coding variants, this tool also integrates allele frequencies and genotype data providing population-specific information from published high quality variation databases such as 1000 Genomes Project.



Data formats

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VCF

The Variant Call Format (VCF) is a tab-delimited text file format to represent a number of different genetic variants including SNPs and Indels. This format was developed as part of the 1000 Genomes Project. A detailed summary of this file format can be found here.


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Interval

The Interval format consists of eight tab-delimited columns and is used to represent genomic intervals such as genes. This format is closely associated with the intervalFind module, which is part of BIOS. This module efficiently finds intervals that overlap with a query interval. The underlying algorithm is based on containment sublists: Alekseyenko, A.V., Lee, C.J. "Nested Containment List (NCList): A new algorithm for accelerating interval query of genome alignment and interval databases" Bioinformatics 2007;23:1386-1393 [1]. 

1.   Name of the interval
2.   Chromosome 
3.   Strand
4.   Interval start (with respect to the "+")
5.   Interval end (with respect to the "+")
6.   Number of sub-intervals
7.   Sub-interval starts (with respect to the "+", comma-delimited)
8.   Sub-interval end (with respect to the "+", comma-delimited)

Example file: 

uc001aaw.1      chr1    +       357521  358460  1       357521  358460
uc001aax.1      chr1    +       410068  411702  3       410068,410854,411258    410159,411121,411702
uc001aay.1      chr1    -       552622  554252  3       552622,553203,554161    553066,553466,554252
uc001aaz.1      chr1    +       556324  557910  1       556324  557910
uc001aba.1      chr1    +       558011  558705  1       558011  558705

In this example the intervals represent a transcripts, while the sub-intervals denote exons.

Note: the coordinates in the Interval format are zero-based and the end coordinate is not included.



List of programs

VAT Core Modules

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snpMapper

snpMapper is a program to annotate a set of SNPs in VCF format. The program determines the effect of a SNP on the coding potential (synonymous, nonsynonymous, prematureStop, removedStop, spliceOverlap) of each transcript of a gene.

Usage: 

snpMapper <annotation.interval> <annotation.fa>
  • Inputs: Takes a VCF input from STDIN
  • Outputs: Outputs annotated SNPs in VCF format. The annotation information is captured as part of the INFO field. For details refer to the VCF format specification.
  • Required arguments
    • annotation.interval - Annotation file representing the genomic coordinates of the gene models in Interval format. Each line in this file represents a transcript. This file is typically generated using the gencode2interval program.
    • annotation.fa - File with the transcript sequences in FASTA format for each entry specified in annotation.interval. This file is typically generated by the interval2sequences program using the 'exonic' mode.
  • Optional arguments
    • None

Note: The name field in the Interval must contain four pieces of information delimited by the '|' symbol (geneId|transcriptId|geneName|transcriptName). Using gencode2interval program ensures proper formatting: 

ENSG00000008513|ENST00000319914|ST3GAL1|ST3GAL1-201	chr8	-	134472009	134488267	6	134472009,134474117,134475656,134477020,134478136,134487961	134472180,134474237,134475702,134477200,134478333,134488267
ENSG00000008513|ENST00000395320|ST3GAL1|ST3GAL1-202	chr8	-	134472009	134488267	6	134472009,134474117,134475656,134477020,134478136,134487961	134472180,134474237,134475702,134477200,134478333,134488267
ENSG00000008513|ENST00000399640|ST3GAL1|ST3GAL1-203	chr8	-	134472009	134488267	6	134472009,134474117,134475656,134477020,134478136,134487961	134472180,134474237,134475702,134477200,134478333,134488267
ENSG00000008516|ENST00000325800|MMP25|MMP25-201	chr16	+	3097544	3105947	4	3097544,3100009,3100254,3105830	3097548,3100145,3100546,3105947
ENSG00000008516|ENST00000336577|MMP25|MMP25-202	chr16	+	3096918	3109096	10	3096918,3097415,3100009,3100254,3107033,3107310,3107531,3108181,3108412,3108827	3097017,3097548,3100145,3100547,3107210,3107395,3107614,3108334,3108670,3109096

The geneId is utilized to determine if multiple transcripts belong to the same gene model.


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snpMapperGeneric

txt

Usage: 

cmd
  • Inputs:
  • Outputs:
  • Required arguments
    • None
  • Optional arguments
    • None


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indelMapper

txt

Usage: 

cmd
  • Inputs:
  • Outputs:
  • Required arguments
    • None
  • Optional arguments
    • None


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vcfSummary

txt

Usage: 

cmd
  • Inputs:
  • Outputs:
  • Required arguments
    • None
  • Optional arguments
    • None


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vcf2images

txt

Usage: 

cmd
  • Inputs:
  • Outputs:
  • Required arguments
    • None
  • Optional arguments
    • None


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vcfSubsetByGene

txt

Usage: 

cmd
  • Inputs:
  • Outputs:
  • Required arguments
    • None
  • Optional arguments
    • None


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vcfModifyHeader

txt

Usage: 

cmd
  • Inputs:
  • Outputs:
  • Required arguments
    • None
  • Optional arguments
    • None


Auxiliary Programs

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gencode2interval

gencode2interval converts a GENCODE annotation file (in GTF format) to the Interval format.

Usage: 

gencode2interval
  • Inputs: Takes a GENCODE annotation file in GTF format from STDIN
  • Outputs: Outputs the GENCODE annotation file in Interval format to STDOUT
  • Required arguments
    • None
  • Optional arguments
    • None

Note: To obtain the coding sequences of the elements with gene_type protein_coding and transcript_type protein_coding the following command should be used: 

awk '/\t(HAVANA|ENSEMBL)\tCDS\t/ {print}' gencode.v3c.annotation.GRCh37.gtf | grep 'gene_type "protein_coding"' | grep 'transcript_type "protein_coding"' > gencode.v3c.annotation.GRCh37.cds.gtpc.ttpc.gtf
gencode2interval < encode.v3c.annotation.GRCh37.cds.gtpc.ttpc.gtf > encode.v3c.annotation.GRCh37.cds.gtpc.ttpc.interval


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interval2sequences

Module to retrieve genomic/exonic sequences for an annotation set in Interval format.

Usage: 

interval2sequences <file.2bit> <file.annotation> <exonic|genomic>
  • Inputs: None
  • Outputs: Reports the extracted sequences in FASTA format
  • Required arguments
    • file.2bit - genome reference sequence in 2bit format
    • file.annotation - annotation set in Interval format (each line represents one transcript)
    • < exonic | genomic > - exonic means that only the exonic regions are extracted, while genomic indicates that the intronic sequences are extracted as well
  • Optional arguments
    • None


Retrieved from "http://info.gersteinlab.org/VAT"
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