首先根据今年发表在Genome Biology上一篇综述总览分析流程:

一、使用Fastqc对fastq 文件的测序质量统计

for i in `ls *fastq`; do echo "fastqc -t 4 -o ./ $i"; done >
nohup ParaFly -c -CPU 18 &

二、Trimmomatic质控(可使用 cutadapt,AdapterRemoval v2,Skewer 和 trimmomatic 等软件)
The forward and reverse adapters are slightly different. We will also trim low quality bases at the ends of the reads (quality less than 20). We will only keep reads that are at least 20 bases long. We remove short reads (< 20bp) as they are not useful, they will either be thrown out by the mapping or may interfere with our results at the end.

mkdir 1.trimmomatic
cd 1.trimmomatic/
for i in `cat ../samples.txt`
    echo "java -jar /opt/biosoft/Trimmomatic-0.38/trimmomatic-0.38.jar PE -threads 20 ../$i.1.fastq ../$i.2.fastq $i.1.fastq $i.1.unpaired.fastq $i.2.fastq $i.2.unpaired.fastq ILLUMINACLIP:/opt/biosoft/Trimmomatic-0.38/adapters/TruSeq3-PE-2.fa:2:30:10 LEADING:3 TRAILING:3 SLIDINGWINDOW:4:15 MINLEN:20 TOPHRED33 2> $i.trimmomatic.log"
done > command.trimmomatic.list
ParaFly -c command.trimmomatic.list -CPU 9
cd ..

三、Mapping Reads to Reference Genome

mkdir 2.bowtie2 && cd 2.bowtie2
bowtie2-build --threads 160 genome.fasta genome
for i in `cat ../samples.txt`
    echo "bowtie2 -x genome -1 ../1.trimmomatic/$i.1.fastq -2 ../1.trimmomatic/$i.2.fastq -p 160 -I 0 -X 1000 --very-sensitive -S $i.bowtie2.sam 2> $i.bowtie2.log"
done > bowtie2.list
ParaFly -c bowtie2.list -CPU 9
for i in `cat ../samples.txt`
    echo "samtools sort -@ 40 -m 8G -o $i.bowtie2.bam -O BAM $i.bowtie2.sam"
done > sam2bam.list
ParaFly -c sam2bam.list -CPU 9
cd ..

四、Filtering Mapped Reads
1、Filter Duplicate Reads

sambamba markdup -r --overflow-list-size 600000  --tmpdir='./' ../2.bowtie2/$i.bowtie2.bam $i.sambamba.rmdup.bam

size of the overflow list where reads, thrown away from the hash table, get a second chance to meet their pairs (default is 200000 reads); increasing the size reduces the number of temporary files created
-r, –remove-duplicates
remove duplicates instead of just marking them
-t, –nthreads=NTHREADS
number of threads to use
External sort is not implemented. Thus, memory consumption grows by 2Gb per each 100M reads. Check that you have enough RAM before running the tool.

2、Filter Uninformative Reads

samtools view -h -f 2 -q 30 $i.sambamba.rmdup.bam |grep -v pilon373| samtools sort -O bam -@ 40 -o - > $i.last.bam
samtools index $i.last.bam
samtools index $i.sambamba.rmdup.bam
samtools flagstat $i.sambamba.rmdup.bam > $i.sambamba.rmdup.stat
samtools flagstat $i.last.bam > $i.last.stat
bedtools bamtobed -i $i.last.bam > $i.bed

3、Check Insert Sizes

for i in `cat ../samples.txt`
    echo "samtools view $i.last.bam |awk '{print $9}'  > $i.last_length.txt"
done > last_bam_length.list
ParaFly -c last_bam_length.list -CPU 9

五、Peak calling(详细参数参考

macs2 callpeak -t ../3.filtering/$i.bed -g 8.9e8 --nomodel --shift -100 --extsize 200 -n $i.peaks --outdir ./



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