Difference between revisions of "UGP Variant Pipeline 0.0.3"

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* Total Sequences (<span style="background:#FFFF00">Need to develop a acceptable range</span>)
 
* Total Sequences (<span style="background:#FFFF00">Need to develop a acceptable range</span>)
 
* Filtered Sequences      (Should be 0 or at least very low)
 
* Filtered Sequences      (Should be 0 or at least very low)
−
* Sequence length (must be ~ 100 bp)
+
* Sequence length (must be >= 100 bp)
 
* %GC    (<span style="background:#FFFF00">should be 45 < x < 55</span>)
 
* %GC    (<span style="background:#FFFF00">should be 45 < x < 55</span>)
 
* Total Duplicate Percentage (<span style="background:#FFFF00">This value may not be valuable - an acceptable range has not been determined</span>).
 
* Total Duplicate Percentage (<span style="background:#FFFF00">This value may not be valuable - an acceptable range has not been determined</span>).
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=== BAM Quality Control ===
 
=== BAM Quality Control ===
  
−
<span style="background:#FFFF00">
+
Via Picards tools CollectMultipleMetrics program
−
CollectAlignmentSummaryMetrics
+
  java -Xmx10g -XX:ParallelGCThreads=10 -Djava.io.tmpdir=/tmp  
−
  java -Xmx10g -XX:ParallelGCThreads=10 -Djava.io.tmpdir=/tmp CollectAlignmentSummaryMetrics.jar
+
    CollectMultipleMetrics.jar  
 
     I=/output/filename.b37_1kg.sorted.bam                                       
 
     I=/output/filename.b37_1kg.sorted.bam                                       
 
     O=/output/filename.b37_1kg.AlignmentSummaryMetrics                         
 
     O=/output/filename.b37_1kg.AlignmentSummaryMetrics                         

Latest revision as of 16:43, 21 August 2014

Utah Genome Project

Variant Calling Pipeline Version 0.0.3

Jan. 2014

Software Versions

    • GenomeAnalysisTK-2.8-1
    • Picard : Version: 1.99
    • FastQC v0.10.1
    • Samtools Version: 0.1.19
    • BWA Version: 0.7.5
    • cApTUrE 0.03

Data Source

Data sets used for the variant calling pipeline come from the Broad GSA (GATK) group as the 'GATK resource bundle 2.5' version 2.8 

wget -r ftp://gsapubftp-anonymous@ftp.broadinstitute.org/bundle/2.5/b37
  • Reference Genome (GRCh37):
    • human_g1k_v37_decoy.fasta
  • VCF files for RealignerTargetCreator knowns and dbsnp for BaseRecalibrator.
    • known_indel: /data/GATK_Bundle/Mills_and_1000G_gold_standard.indels.b37.vcf
    • known_indel: /data/GATK_Bundle/1000G_phase1.indels.b37.vcf
    • known_dbsnp: /data/GATK_Bundle/dbsnp_137.b37.vcf
  • 1000Genomes Background BAMS ran concurrently with UnifiedGenotyper
    • CEU
    • GBR
  • Resource files for VariantRecalibrator_SNP
    • hapmap_3.3.b37.vcf
    • 1000G_omni2.5.b37.vcf
    • 1000G_phase1.snps.high_confidence.b37.vcf
  • Resource files for VariantRecalibrator_INDEL
    • Mills_and_1000G_gold_standard.indels.b37.vcf
    • 1000G_phase1.indels.b37.vcf

Sequencing

This pipeline is designed for 100 bp (or greater) Illumina HiSeq PE exome or WGS sequence data with Sanger/Illumina 1.9 quality encoding, and uses Illumina naming convention found here [1]

Validate File Integrity with md5sum

An md5sum signature should be provided for each FastQ file by the sequencing center. After the file has been downloaded, locally check the md5sum to be sure that no data corruption occurred during the file transfer. 

md5sum file.fastq > file_local.md5
diff file_local.md5 file_provided.md5

If the md5sum signature differs from that provided for the file:

  • Check to be sure you have the correct file.
  • Check if the md5sum was calculated on that compressed or uncompressed file by the provider and be sure to do the same with the local copy.
  • Try the download again.
  • Contact the sequence provider.

FastQ File Analyses

fastqc Sample1_L1_R1.txt

From the fastqc_data.txt file we check the following values:

  • Encoding (must be Sanger / Illumina 1.9)
  • Total Sequences (Need to develop a acceptable range)
  • Filtered Sequences (Should be 0 or at least very low)
  • Sequence length (must be >= 100 bp)
  • %GC (should be 45 < x < 55)
  • Total Duplicate Percentage (This value may not be valuable - an acceptable range has not been determined).

Alignment

Align reads to the genome with bwa.

Index the reference sequence if this has not already been done 

bwa index -a bwtsw human_g1k_v37_decoy.fasta

The 'bwa aln' program will find the reference coordinates of the input reads (independent of their mate-pair). The following parameters are those used by the 1KG project for aligning Illumina data. 

bwa aln -q 15 human_g1k_v37_decoy.fasta file.fastq > Sample1_L1_R1.sai # One lane of reads first in pair
bwa aln -q 15 human_g1k_v37_decoy.fasta file.fastq > Sample1_L1_R2.sai # One lane of reads second in pair

The 'bwa sampe'. For paired-end reads, the maximum insert size is taken to be 3 times the expected insert size. 

bwa sampe -r "read group" -P Sample1_L1_R1.sai Sample1_L1_R1.sai Sample1_L1_R1.fastq Sample1_L1_R2.fastq | samtools view -bSho BAM_FILE -

This will switch to bwa mem soon. 

bwa mem -M -R "read group" human_g1k_v37_decoy.fasta Sample1_L1_R1.fq Sample1_L1_R2.fq | samtools view -bSho BAM_FILE -

BAM File Analyses

Alignment BAM files are improved in various ways to help increase the quality and speed of subsequent variant calling steps.

Merge lane level BAMs to individual

java -Xmx10g -XX:ParallelGCThreads=10 -Djava.io.tmpdir=/tmp MergeSamFiles.jar
    INPUT=Sample1_L1.rg.bam                     
    INPUT=Sample1_L2.rg.bam                    
    OUTPUT=Sample1.bam                          
    VALIDATION_STRINGENCY: LENIENT
    MAX_RECORDS_IN_RAM: 5000000
    CREATE_INDEX: True
    SORT_ORDER: coordinate
    ASSUME_SORTED: True 
    USE_THREADING: True
    2> MergeSamFiles.report

Mark Duplicates

Remove PCR/Optical duplicate reads 

java -Xmx10g -XX:ParallelGCThreads=10 -Djava.io.tmpdir=/tmp MarkDuplicates.jar
   INPUT=Sample1.bam                   
   OUTPUT=Sample1.dedup.bam            
   METRICS_FILE=lane1_dup_metrics.txt  
   VALIDATION_STRINGENCY: LENIENT
   MAX_RECORDS_IN_RAM: 5000000
   CREATE_INDEX: True
   ASSUME_SORTED: True       
   2> MarkDuplicates.log

Develop range for duplicate levels here

Local Realignment of Indels

java -Xmx10g -Djava.io.tmpdir=/tmp GenomeAnalysisTK.jar
   -I dedup_bam.list                                    
   -o Realign_Intervals.txt                            
   -T RealignerTargetCreator                           
   -R human_g1k_v37_decoy.fasta                              
   -known [list from above]
   -nt 24                                              
   2> RealignerTargetCreator.log

Base Quality Score Recalibration

java -Xmx10g -Djava.io.tmpdir=/tmp GenomeAnalysisTK.jar
  -T PrintReads                       
  -I Sample1.realign.bam              
  -o Sample1.recal.bam                
  -R human_g1k_v37_decoy.fasta              
  -BQSR recalibration_report.grp

BAM Quality Control

Via Picards tools CollectMultipleMetrics program 

java -Xmx10g -XX:ParallelGCThreads=10 -Djava.io.tmpdir=/tmp 
   CollectMultipleMetrics.jar 
   I=/output/filename.b37_1kg.sorted.bam                                      
   O=/output/filename.b37_1kg.AlignmentSummaryMetrics                         
   R= human_g1k_v37_decoy.fasta                                                    
   VALIDATION_STRINGENCY=LENIENT                                             
   PROGRAM: QualityScoreDistribution

ReduceReads

java -Xmx10g -XX:ParallelGCThreads=10 -Djava.io.tmpdir=/tmp GenomeAnalysisTK.jar
  -T ReduceReads
  -I Sample1.recal.bam
  -o Sample1.reduced.bam
  -R human_g1k_v37_decoy.fasta
  2> ReduceReads.report

Variant Calling

UnifiedGenotyper

SNP calling 

java -Xmx10g -Djava.io.tmpdir=/tmp GenomeAnalysisTK.jar
  -T UnifiedGenotyper                  
  -I reduced_bam.list
  -I 1000G background_bam.list
  -o Sample1.raw.vcf                  
  -R human_g1k_v37_decoy.fasta
  -nt 4
  -nct 6
  -stand_call_conf 30.0
  -stand_emit_conf 30.0
  -glm SNP   
  -out_mode EMIT_VARIANTS_ONLY
  -L NCBI Ref_GRCh37 region.bed 
  2> UnifiedGenotyper.report

INDEL calling 

java -Xmx10g -Djava.io.tmpdir=/tmp GenomeAnalysisTK.jar
  -T UnifiedGenotyper                  
  -I reduced_bam.list
  -I 1000G background_bam.list
  -o Sample1.raw.vcf                  
  -R human_g1k_v37_decoy.fasta
  -nt 4
  -nct 6
  -stand_call_conf 30.0
  -stand_emit_conf 30.0
  -glm INDEL   
  -out_mode EMIT_VARIANTS_ONLY
  -L NCBI Ref_GRCh37 region.bed 
  2> UnifiedGenotyper.report

VariantRecalibrator

SNP Recalibration 

java -Xmx10g -Djava.io.tmpdir=/tmp GenomeAnalysisTK.jar
  -T VariantRecalibrator
  -R human_g1k_v37_decoy.fasta
  -input Sample1.raw.vcf
  -nt 25
  -resource: hapmap,known=false,training=true,truth=true,prior=15.0
  -resource: omni,known=false,training=true,truth=true,prior=12.0
  -resource: 1000G,known=false,training=true,truth=false,prior=10.0
  -use_annotation: QD
  -use_annotation: HaplotypeScore
  -use_annotation: MQRankSum
  -use_annotation: ReadPosRankSum
  -use_annotation: FS
  -numBadVariants: 5000
  -mode SNP                           
  -recalFile Sample1_SNP.recal            
  -tranchesFile Sample1_SNP.tranches      
  -rscriptFile Sample1_SNP.plots.R       
  2> VariantRecalibrator_SNP.report

INDEL Recalibration 

java -Xmx10g -Djava.io.tmpdir=/tmp GenomeAnalysisTK.jar
  -T VariantRecalibrator
  -R human_g1k_v37_decoy.fasta
  -input Sample1.raw.vcf
  -nt 25
  -resource: mills,known=false,training=true,truth=true,prior=12.0
  -resource: 1000G,known=false,training=true,truth=true,prior=10.0
  -use_annotation: MQRankSum
  -use_annotation: ReadPosRankSum
  -use_annotation: FS
  -numBadVariants: 5000
  -mode INDEL
  -recalFile Sample1_INDEL.recal            
  -tranchesFile Sample1_INDEL.tranches      
  -rscriptFile Sample1_INDEL.plots.R       
  2> VariantRecalibrator_INDEL.report

ApplyRecalibration

SNP Apply 

java -Xmx10g -Djava.io.tmpdir=/tmp GenomeAnalysisTK.jar
  -T ApplyRecalibration
  -input Sample1_raw_SNP.vcf
  -o Sample1_vqsr_SNP.vcf
  -R human_g1k_v37_decoy.fasta
  -nt 25
  -ts_filter_level: 99.0
  -excludeFiltered : TRUE
  -tranchesFile Sample1.tranches
  -recalFile Sample1.recal
  -mode SNP 
  2> ApplyRecalibration_SNP.report

SNP INDEL 

java -Xmx10g -Djava.io.tmpdir=/tmp GenomeAnalysisTK.jar
  -T ApplyRecalibration
  -input Sample1_raw_INDEL.vcf
  -o Sample1_vqsr_INDEL.vcf
  -R human_g1k_v37_decoy.fasta
  -nt 25
  -ts_filter_level: 99.0
  -excludeFiltered : TRUE
  -tranchesFile Sample1.tranches
  -recalFile Sample1.recal
  -mode INDEL 
  2> ApplyRecalibration_INDEL.report

SelectVariants

These commands will remove the background files and output SNP and INDEL files, then combine them into a single VCF file.

Select SNP 

java -Xmx10g -Djava.io.tmpdir=/tmp GenomeAnalysisTK.jar
  -T SelectVariants
  -R human_g1k_v37_decoy.fasta
  --variant SNP_variant 
  -o output_SNP.file 
  2> SelectVariants_SNP.report

Select INDEL 

java -Xmx10g -Djava.io.tmpdir=/tmp GenomeAnalysisTK.jar
  -T SelectVariants
  -R human_g1k_v37_decoy.fasta
  --variant INDEL_variant 
  -o output_INDEL.file 
  2> SelectVariants_INDEL.report

CombineVarients 

java -Xmx10g -Djava.io.tmpdir=/tmp GenomeAnalysisTK.jar
  -T CombineVariants
  -R human_g1k_v37_decoy.fasta
  --variant INDEL_variant 
  --variant  output_INDEL.file
  --variant output_SNP.file
  -o Final.vcf 
  2> CombineVarients.report

Variant File QC

Quality Metrics on variants

  • Ti/Tv Ratio (2.1 for WGS ~2.8 for exome)
  • HapMap concordance
  • SNV/Indel Counts
  • Rare variant enrichment
  • DP
  • Q
  • GQ
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