一个高杂合真菌基因组组装脚本（改代码版）

作者: IMC小达人 | 来源:发表于2019-10-31 11:02 被阅读0次

前言及背景

什么是基因组de novo测序？其是对某一物种进行高通量测序，利用高性能计算平台和生物信息学方法，在不依赖于参考基因组的情况下进行组装，从而绘制该物种的全基因组序列图谱。针对基因组的特性，基因组常被分为两类：普通（简单）基因组和复杂基因组。简单基因组指单倍体，纯合二倍体或者杂合度<0.5%，且重复序列含量<50%，GC含量为35%到65%之间的二倍体。复杂基因组则指杂合率＞0.5%，重复序列含量＞50%，GC含量处于异常的范围（GC含量＜35%或者GC含量＞＝65%的二倍体，多倍体。诺禾致源对二倍体复杂基因组进一步细分为微杂合基因组（0.5%＜杂合率＜＝0.8%、高杂合基因组（杂合率＞0.8%）以及高重复基因组（重复序列比例>50%）。复杂基因组的组装一直以来都是一个让科研工作者为之头疼的问题。科研工作者也为解决这个问题一直努力着。随着三代测序平台的更迭，测序subreads的长度不断的增长，以及光学图谱技术的出现（Hic,10xGenomic等）。重复序列导致的组装困难逐步被缓解。但高杂合这一特性任一直困扰着科研工作者。

为了解决杂合组装，各式各样的方案不断被提出。总体思路有下：1.设计实验方案获取单倍型（例如种间杂种；案例：Sequencing a Juglans regia × J. microcarpa hybrid yields high-quality genome assemblies of parental species；2.设计适合于杂合基因组组装的软件，优化组装的算法；3.组装之后，再用去杂合软件去除杂合序列。

第一个思路很清晰，获取单倍型再测序，就解决了高杂合这个难点，可有时单倍体的获取真不是一般的难，局限性很大。

基于第二个思路，已有很多软件开发。有NOVOheter, Plantanus, MSR-CA，Plantanus-allee（Plantanus的升级版，支持Hic，10xGenomics等数据）等。此外还有一些软件有支持高杂合组装的模块，如Canu，SPAdes, Falon等。但实测的经验来看，效果都不是很好。

第三种思路的核心就是，居于相似性cut，目前接触过的有Redundans，Haplomerger2，Purge_haplogs。Purge_haplogs除了考虑相似性，还有一大特性，就是通过分析比对read的覆盖度决定谁去谁留。此外，Haplomerger2和Purge_haplogs还支持重复序列部分的屏蔽。

今年我接手到了一个基因组大小为86M,杂合率约2.4%，重复序列率约为20%左右的真菌。测序策略为pacbio seq I + PE 150 。本来打算再做一个Hic，但咨询一些测序公司之后，均表示真菌没有太多成功经验，且投入与产出可能不对等。故打消测Hic的念头。

基于已有的数据，我先采取了canu （单倍型组装；canu多倍体模式，"batOptions=-dg 3 -db 3 -dr 1 -ca 500 -cp 50"组装），MECAT2，MaSuRCA，Falon，flye，wtdbg2 等组装软件进行了组装。接着使用 Purge_haplogs 、Redundans和Haplomerger2进行去杂合，然后再使用 FinisherSC进行基因组升级，最后使用nextpolish 进行 polish。经过测试，canu，MECAT2（经过nextpolish 进行 polish之后）， MaSuRCA的三个软件的表现相对较好。去杂软件Purge_haplogs的适用性优于Redundans和Haplomerger2，去杂前后BUSCO评估基本不变。由于涉及到文章。故暂时只能先提供最优的脚本，等文章出了之后会进一步深入。

组装案例


#测序数据Bam to Fastq or Fasta

samtools fastq -0 012m.subreads.fq -@ 32 subreads.bam

#Assessment of genome size and heterozygosity(raw PE reads)

mkdir genomescope

cd genomescope

ln -s ../012m_L1_?.fq ./

jellyfish count -C -m 21 -s 1000000000 -t 32 *.fq -o reads.jf

jellyfish histo -t 32 reads.jf > reads.histo

Rscript /opt/biosoft/genomescope/genomescope.R reads.histo 21 150 output

# 二代数据质控

mkdir Trimmomatic

cd Trimmomatic

java -jar /opt/biosoft/Trimmomatic-0.36/trimmomatic-0.36.jar PE -threads 32 -phred33 ../012m_L1_1.fq ../012m_L1_2.fq 012m_Trimmomatic.1.fq 012m_Trimmomatic.unpaired.1.fq 012m_Trimmomatic.2.fq 012m_Trimmomatic.unpaired.2.fq ILLUMINACLIP:/opt/biosoft/Trimmomatic-0.36/adapters/TruSeq3-PE-2.fa:2:30:10 LEADING:3 TRAILING:3 SLIDINGWINDOW:4:20 MINLEN:75 TOPHRED33

cd ../

# correct Illumina reads | Assessment of genome size and heterozygosity

mkdir Finderrors

source ~/.bash.pacbio

# ErrorCorrectReads.pl 为 ALLPATHS-LG 的一个perl 程序

ErrorCorrectReads.pl PHRED_ENCODING=33 READS_OUT=012m FILL_FRAGMENTS=0 KEEP_KMER_SPECTRA=1 PAIRED_READS_A_IN=../fastuniq/012m.fastuniq.1.fastq PAIRED_READS_B_IN=../fastuniq/012m.fastuniq.2.fastq PLOIDY=2 PAIRED_SEP=251 PAIRED_STDEV=48

# ErrorCorrectReads.pl也可以对基因组特性进行评估，但针对我的菌株来说，同已发布的邻近菌株比较，GenomeScope的结果要准确一些。

# kmer plot

cd 012m.fastq.kspec

perl -p -i -e 's/\@fns = \(\"frag_reads_filt.25mer.kspec\", \"frag_reads_edit.24mer.kspec\", \"frag_reads_corr.25mer.kspec\"\);\n//' /opt/biosoft/ALLPATHS-LG/bin/KmerSpectrumPlot.pl

KmerSpectrumPlot.pl SPECTRA=1 FREQ_MAX=255

perl -p -i -e 's/\@fns = \(\"frag_reads_filt.25mer.kspec\", \"frag_reads_edit.24mer.kspec\", \"frag_reads_corr.25mer.kspec\"\);\n//' /opt/biosoft/ALLPATHS-LG/bin/KmerSpectrumPlot.pl

convert kmer_spectrum.cumulative_frac.log.lin.eps kmer_spectrum.cumulative_frac.log.lin.png

convert kmer_spectrum.distinct.lin.lin.eps kmer_spectrum.distinct.lin.lin.png

convert kmer_spectrum.distinct.log.log.eps kmer_spectrum.distinct.log.log.png

cd ../

# Using LoRDEC to modify PacBio Reads

mkdir LoRDEC

cd LoRDEC

lordec-correct -2 ../Finderrors/012m.paired.A.fastq ../Finderrors/012m.paired.B.fastq -i ../012m.subreads.fq -k 19 -o pacbio.LoRDEC.corrected.fasta -s 3 -T 32 &> lordec-correct.log

seqkit seq -u pacbio.LoRDEC.corrected.fasta > pacbio.corrected.fasta**

cd ../

###Genome assembly###

mkdir MaSuRCA

cd MaSuRCA

echo '# example configuration file

DATA

#Illumina paired end reads supplied as <two-character prefix> <fragment mean> <fragment stdev> <forward_reads> <reverse_reads>

#if single-end, do not specify <reverse_reads>

#MUST HAVE Illumina paired end reads to use MaSuRCA

PE= pe 251 48 /home/bioinfo/data/012m/012m_L1_1.fq  /home/bioinfo/data/012m/012m_L1_2.fq

#Illumina mate pair reads supplied as <two-character prefix> <fragment mean> <fragment stdev> <forward_reads> <reverse_reads>

#JUMP= sh 3600 200 /FULL_PATH/short_1.fastq  /FULL_PATH/short_2.fastq

#pacbio OR nanopore reads must be in a single fasta or fastq file with absolute path, can be gzipped

#if you have both types of reads supply them both as NANOPORE type

PACBIO=/home/bioinfo/data/012m/LoRDEC/pacbio.corrected.fasta

#NANOPORE=/FULL_PATH/nanopore.fa

#Other reads (Sanger, 454, etc) one frg file, concatenate your frg files into one if you have many

#OTHER=/FULL_PATH/file.frg

#synteny-assisted assembly, concatenate all reference genomes into one reference.fa; works for Illumina-only data

#REFERENCE=/FULL_PATH/nanopore.fa

END

PARAMETERS

#PLEASE READ all comments to essential parameters below, and set the parameters according to your project

#set this to 1 if your Illumina jumping library reads are shorter than 100bp

EXTEND_JUMP_READS=0

#this is k-mer size for deBruijn graph values between 25 and 127 are supported, auto will compute the optimal size based on the read data and GC content

GRAPH_KMER_SIZE = auto

#set this to 1 for all Illumina-only assemblies

#set this to 0 if you have more than 15x coverage by long reads (Pacbio or Nanopore) or any other long reads/mate pairs (Illumina MP, Sanger, 454, etc)

USE_LINKING_MATES = 0

#specifies whether to run the assembly on the grid

USE_GRID=0

#specifies grid engine to use SGE or SLURM

GRID_ENGINE=SGE

#specifies queue (for SGE) or partition (for SLURM) to use when running on the grid MANDATORY

GRID_QUEUE=all.q

#batch size in the amount of long read sequence for each batch on the grid

GRID_BATCH_SIZE=500000000

#use at most this much coverage by the longest Pacbio or Nanopore reads, discard the rest of the reads

#can increase this to 30 or 35 if your reads are short (N50<7000bp)

LHE_COVERAGE=25

#set to 0 (default) to do two passes of mega-reads for slower, but higher quality assembly, otherwise set to 1

MEGA_READS_ONE_PASS=0

#this parameter is useful if you have too many Illumina jumping library mates. Typically set it to 60 for bacteria and 300 for the other organisms

#LIMIT_JUMP_COVERAGE = 300

#these are the additional parameters to Celera Assembler.  do not worry about performance, number or processors or batch sizes -- these are computed automatically.

#CABOG ASSEMBLY ONLY: set cgwErrorRate=0.25 for bacteria and 0.1<=cgwErrorRate<=0.15 for other organisms.

CA_PARAMETERS =  cgwErrorRate=0.15

#CABOG ASSEMBLY ONLY: whether to attempt to close gaps in scaffolds with Illumina  or long read data

CLOSE_GAPS=1

#auto-detected number of cpus to use, set this to the number of CPUs/threads per node you will be using

NUM_THREADS = 32

#this is mandatory jellyfish hash size -- a safe value is estimated_genome_size*20**

JF_SIZE = 1740000000

#ILLUMINA ONLY. Set this to 1 to use SOAPdenovo contigging/scaffolding module.  Assembly will be worse but will run faster. Useful for very large (>=8Gbp) genomes from Illumina-only data

SOAP_ASSEMBLY=0

#Hybrid Illumina paired end + Nanopore/PacBio assembly ONLY.  Set this to 1 to use Flye assembler for final assembly of corrected mega-reads.  A lot faster than CABOG, at the expense of some contiguity. Works well even when MEGA_READS_ONE_PASS is set to 1.  DO NOT use if you have less than 15x coverage by long reads.

FLYE_ASSEMBLY=0

END ' > config.txt

/opt/biosoft/MaSuRCA-3.3.4/bin/masurca config.txt

./assemble.sh

mkdir purge_haplogs

cd purge_haplogs

minimap2 -t 32 -ax map-pb ../final.genome.scf.fasta /home/bioinfo/data/012m/canu/012m.correctedReads.fasta.gz | samtools view -hF 256 - | samtools sort -@ 32 -m 2G -o aligned.bam

purge_haplotigs  hist  -b aligned.bam  -g ../final.genome.scf.fasta -t 20

purge_haplotigs contigcov -i aligned.bam.gencov -o coverage_stats.csv -l 18 -m 76 -h 134

purge_haplotigs purge -g ../final.genome.scf.fasta -c coverage_stats.csv -b aligned.bam -t 4 -a 50

mkdir finisherSC

cd finisherSC

ln -s ../curated.fasta ./contigs.fasta

ln -s ~/data/012m/canu/012m.correctedReads.fasta ./raw_reads.fasta

#这一步不要设置多线程，不然可能报错，使用mummer4的速度要远高于mummet3

python /opt/biosoft/finishingTool/finisherSC.py ./ /opt/biosoft/mummer4/bin/

mkdir NextPolish

cd NextPolish

ls ~/data/012m/Finderrors/012m.paired.?.fastq > sgs.fofn

echo '/home/bioinfo/data/012m/canu/012m.correctedReads.fasta' > lgs.fofn

echo '[General]

job_type = local

job_prefix = nextPolish

task = default

rewrite = yes

rerun = 10

parallel_jobs = 5

multithread_jobs = 6

genome = ../improved3.fasta

genome_size = auto

workdir = ./01_rundir

polish_options = -p {multithread_jobs}

[sgs_option]

sgs_fofn = ./sgs.fofn

sgs_options = -max_depth 100 -bwa

[lgs_option]

lgs_fofn = ./lgs.fofn

lgs_options = -min_read_len 10k -max_read_len 150k -max_depth 60

lgs_minimap2_options = -x map-pb

[polish_options]

-ploidy 2 ' > run.cfg

/opt/biosoft/NextPolish/nextPolish run.cfg

cat ./01_rundir/01.kmer_count/*polish.ref.sh.work/polish_genome*/genome.nextpolish.part*.fasta > genome.nextpolish.fasta