加速体细胞突变检测分析流程-系列2（ctDNA等高深度样本）

Sentieon●体细胞变异检测系列-2

Sentieon 致力于解决生物信息数据分析中的速度与准确度瓶颈，通过算法的深度优化和企业级的软件工程，大幅度提升NGS数据处理的效率、准确度和可靠性。

针对体细胞变异检测，Sentieon软件提供两个模块：TNscope和TNhaplotyer2。

TNscope：此模块使用Sentieon特有的算法，拥有更快的计算速度（提速10倍+）和更高的计算精度，对临床基因诊断样本尤其适用；

TNhaplotyper2：此模块匹配Mutect2（现在匹配到4.1.9）结果的同时，计算速度提升10倍以上。

ctDNA变异检测分析

以下给出的步骤脚本，主要针对ctDNA和其他高深度测序的样本数据(2000-5000x depth, AF > 0.3%)

第一步：Alignment

# ******************************************
# 1a. Mapping reads with BWA-MEM, sorting for tumor sample
# ******************************************
( sentieon bwa mem -M -R "@RG\tID:$tumor\tSM:$tumor\tPL:$platform" \
-t $nt -K 10000000 $fasta $tumor_fastq_1 $tumor_fastq_2 || \
echo -n 'error' ) | \
sentieon util sort -o tumor_sorted.bam -t $nt --sam2bam -i -

# ******************************************
# 1b. Mapping reads with BWA-MEM, sorting for normal sample
# ******************************************
( sentieon bwa mem -M -R "@RG\tID:$normal\tSM:$normal\tPL:$platform" \
-t $nt -K 10000000 $fasta $normal_fastq_1 $normal_fastq_2 ||
echo -n 'error' ) | \
sentieon util sort -o normal_sorted.bam -t $nt --sam2bam -i -

第二步：PCR Duplicate Removal (Skip For Amplicon)

# ******************************************
# 2a. Remove duplicate reads for tumor sample.
# ******************************************
# ******************************************
sentieon driver -t $nt -i tumor_sorted.bam \
      --algo LocusCollector \
      --fun score_info \ tumor_score.txt sentieon driver -t $nt -i tumor_sorted.bam \
      --algo Dedup \
      --score_info tumor_score.txt \
      --metrics tumor_dedup_metrics.txt \ tumor_deduped.bam
# ******************************************
# 2b. Remove duplicate reads for normal sample.
# ******************************************
sentieon driver -t $nt -i normal_sorted.bam \
     --algo LocusCollector \
     --fun score_info \ normal_score.txt sentieon driver -t $nt -i normal_sorted.bam \
     --algo Dedup \
     --score_info normal_score.txt \
     --metrics normal_dedup_metrics.txt \ normal_deduped.bam

第三步: Base Quality Score Recalibration (Skip For Small Panel)

# ******************************************
# 3a. Base recalibration for tumor sample
# ******************************************
sentieon driver -r $fasta -t $nt -i tumor_deduped.bam --interval $BED \
    --algo QualCal \
    -k $dbsnp \
    -k $known_Mills_indels \
    -k $known_1000G_indels \ tumor_recal_data.table
# ******************************************
# 3b. Base recalibration for normal sample
# ******************************************
sentieon driver -r $fasta -t $nt -i normal_deduped.bam --interval $BED \
     --algo QualCal \
     -k $dbsnp \
     -k $known_Mills_indels \
     -k $known_1000G_indels \
     normal_recal_data.table

第四步：Variant Calling (Tumor Only)

sentieon driver -r $fasta -t $nt -i tumor_deduped.bam --interval $BED --interval_padding 10 \
     --algo TNscope \
     --tumor_sample $TUMOR_SM \
     --dbsnp $dbsnp \
     --disable_detector sv \
     --min_tumor_allele_frac 3e-3 \
     --filter_t_alt_frac 3e-3 \
     --clip_by_minbq 1 \
     --min_init_tumor_lod 3.0 \
     --min_tumor_lod 3.0 \
     --assemble_mode 4 \
     --resample_depth 100000 \
     [--pon panel_of_normal.vcf \]
     output_tnscope.pre_filter.vcf.gz

第五步：Variant Filtration (Tumor Only)

bcftools annotate -x "FILTER/triallelic_site" output_tnscope.pre_filter.vcf.gz | \
   bcftools filter -m + -s "low_qual" -e "QUAL < 10" | \
   bcftools filter -m + -s "short_tandem_repeat" -e "RPA[0]>=10" | \
   bcftools filter -m + -s "read_pos_bias" -e "FMT/ReadPosRankSumPS[0] < -5" | \
   bcftools norm -f $fasta -m +any | \
sentieon util vcfconvert - output_tnscope.filtered.vcf.gz