Hi all, I am working with Human sample WGS data (30X, PE reads, HiSeq platform) and facing problem at VQSR and variant annotation step. I ran following commands (modified here, path deleted) to get my files, please see my 2 questions after these commands:

1. Converted each sample's bam file into gVCF using GATK's HaplotypeCaller (-ERC GVCF function) for joint genotyping and VQSR, command:

/usr/bin/java -jar /opt/GenomeAnalysisTK.jar \
                        -R ucsc.hg19.fasta \
                        -T HaplotypeCaller \
                        -I ETH003388_final.bam \
                        -D rs_snp.vcf \
                        -ERC GVCF \
                        -variant_index_type LINEAR \
                        -variant_index_parameter 128000 \
                        --alleles rs_snp.vcf \
                        --max_alternate_alleles 3 \
                        -L rs_snp.vcf \
                        -ip 150 \
                        -o ETH003388.g.vcf \
                        -stand_call_conf 0 \
                        -stand_emit_conf 0 

(where rs_snp.vcf is customized dbSNP.vcf with only variants having a SNP rsID).
2. Combined all my individual sample's g.vcf file to form a cohort.g.vcf, command :

/usr/bin/java -jar /opt/GenomeAnalysisTK.jar \
                    -T CombineGVCFs \
                    -R ucsc.hg19.fasta \
                    -D rs_snp.vcf \
                    -o cohort.g.vcf \
                    --variant sample1.g.vcf \
                    --variant sample2.g.vcf \
                    --variant sample3.g.vcf \
                    ........ \
                    --variant sampleN.g.vcf 

3. Converted cohort.g.vcf to genotype.g.vcf, command:

/usr/bin/java  -jar /opt/GenomeAnalysisTK.jar \
                -T GenotypeGVCFs \
                -R ucsc.hg19.fasta \
                -D rs_snp.vcf \
                -allSites \
                -stand_call_conf 0 \
                -stand_emit_conf 0 \
                -maxAltAlleles 3 \
                --variant cohort.g.vcf \
                -o genotype.g.vcf 

4. Running VariantRecalibrator command

/usr/bin/java  -jar /opt/GenomeAnalysisTK.jar \
                    -T VariantRecalibrator \
                    -R ucsc.hg19.fasta \
                    -input genotype.g.vcf \
                    -resource:hapmap,known=false,training=true,truth=true,prior=15.0 hapmap_3.3.hg19.sites.vcf \
                    -resource:omni,known=false,training=true,truth=true,prior=12.0 1000G_omni2.5.hg19.sites.vcf \
                    -resource:1000G,known=false,training=true,truth=false,prior=10.0 1000G_phase1.snps.high_confidence.hg19.sites.vcf \
                    -resource:dbsnp,known=true,training=false,truth=false,prior=2.0 rs_snp.vcf \
                    -an DP \
                    -an QD \
                    -an MQ \
                    -an MQRankSum \
                    -an ReadPosRankSum \
                    -an FS \
                    -an SOR \
                    -an InbreedingCoeff \
                    -mode SNP \
                    -tranche 100.0 \
                    -tranche 99.9 \
                    -tranche 99.0  \
                    -tranche 90.0 \
                    -recalFile recalibrate_SNP.recal \
                    -tranchesFile recalibrate_SNP.tranches \
                    -rscriptFile recalibrate_SNP_plots.R

Question 1: I am getting all my Variants in "False Positive" category in 'recalibrate_SNP.tranches.pdf'. Any idea why all my variants are falling in FP category ?.

Question 2. How can i annotate variants in genotype.g.vcf (of filtered.vcf file after ApplyRecalibration step) in order to get Nonsynonmous SNPs with their respective genotype information in all samples at a time ?. I have done variant annotation of individual sample.vcf files using 'Annovar' but never on combined.g.vcf file, any suggestion will be much appreciated.