0%

基因组质量评估:(五)mapping法:2. samtools计算mapping rate

1. mapping rate

通过mapping把reads与组装好的基因组进行alignment,然后分析mapped reads的sam/bam格式文件,统计mapping rate来评估基因组组装质量。期望mapping rate越接近100%,组装质量越高。

2. Hisat2统计的mapping rate

运行Hisat2对RNA-seq进行mapping时生成的log文件hisat.log会保存着比对的mapping rate信息。

  1. hisat2比对统计结果hisat.log示例
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
19429766 reads; of these: # reads总数
19429766 (100.00%) were paired; of these: # 配对的reads数量
1066192 (5.49%) aligned concordantly 0 times # 一致地比对了0次的reads数量
14853850 (76.45%) aligned concordantly exactly 1 time # 一致地比对了1次的reads数量
3509724 (18.06%) aligned concordantly >1 times # 一致地比对了大于1次的reads数量
----
1066192 pairs aligned concordantly 0 times; of these: # 一致地比对了0次的reads数量中:
54954 (5.15%) aligned discordantly 1 time # 不一致地比对了1次的reads数量
----
1011238 pairs aligned 0 times concordantly or discordantly; of these: #一致或不一致地比对了0次的reads数量中:
2022476 mates make up the pairs; of these: # 配对的reads数量中:
1211647 (59.91%) aligned 0 times #比对0次的数量
607196 (30.02%) aligned exactly 1 time #比对1次的数量
203633 (10.07%) aligned >1 times #比对大于1次的数量
96.88% overall alignment rate # mapping rate,由mapped reads number/total reads number的比例计算得到
[bam_sort_core] merging from 20 files and 4 in-memory blocks...
  1. hisat2结果解释
  • hisat.log结果中,19429766 reads; of these:及大部分包含的信息中,双端测序的reads是只统计一次的。比如19429766 reads代表的是有19429766对双端测序的reads,总reads数量是$19429766*2=38859532$条。
  • 2022476 mates make up the pairs; of these:及之后包含的信息中,代表配对的reads数量,双端测序的reads是统计了配对的所有reads,总reads数量就是2022476条。
  1. hisat2的mapping rate的计算

96.88%的overall alignment rate即为mapping rate,计算方法是:

$$mapping rate=mapped reads number/total reads number$$

  • total reads number用的$19429766*2$。
  • mapped reads number包含:concordantly exactly 1 time(14853850*2),aligned concordantly >1 times(3509724*2),aligned discordantly 1 time(54954*2),mates make up the pairs中的aligned exactly 1 time(607196)和aligned >1 times(203633)。

$$mapping rate=((14853850+3509724+54954)*2+607196+203633)/(19429766*2) = 37647885/38859532*100%=96.88%$$

  • mapped reads number的另一种计算方法:concordantly exactly 1 time(14853850),aligned concordantly >1 times(3509724),aligned concordantly 0 times(1066192)中aligned到的所有reads,即除了aligned concordantly 0 times(1066192)中的aligned 0 times(1211647/2)以外的所有reads。

$$mapping rate=(14853850+3509724+54954+1066192-(1211647/2))/19429766*100%=96.88%$$

3. samtools flagstat统计mapping rate

  1. samtools flagstat
  • 如果hisat2运行时未保存log文件,也可以用samtools flagstat来计算reads的mapping统计值。
  • illumina reads和Pacbio reads等的sam/bam文件也可以用这种方式统计mapping rate。
  • flagstat统计结果中,记录的是sam/bam文件中reads的记录数量,即mapping record rate(双端测序包含配对的所有reads)。
  1. samtools flagstat统计
  • samtools flagstat output.bam > output.flagstat
  1. output.flagstat的结果示例
1
2
3
4
5
6
7
8
9
10
11
12
13
51231959 + 0 in total (QC-passed reads + QC-failed reads) #共有51231959条reads通过QC+0条reads未通过QC,后面的信息行中+后的都是代表QC没通过的reads的数量。
12372427 + 0 secondary
0 + 0 supplementary
0 + 0 duplicates
50020312 + 0 mapped (97.63% : N/A) # 97.63%比例的reads mapping到参考序列上,这就是mapping record rate
38859532 + 0 paired in sequencing
19429766 + 0 read1 # 双端reads中read1的总数
19429766 + 0 read2 # 双端reads中read2的总数
36727148 + 0 properly paired (94.51% : N/A) # 94.51%比例的reads成对的映射上
37160066 + 0 with itself and mate mapped # read映射上但配对read没映射上的数量
487819 + 0 singletons (1.26% : N/A) # 1.26%比例的read没映射上的同时,配对read映射上了
289948 + 0 with mate mapped to a different chr # reads和配对reads映射到不同染色体的情况下的reads数量
205767 + 0 with mate mapped to a different chr (mapQ>=5) # reads和配对reads映射到不同染色体,且映射质量大于等于5的情况下的reads数量
  1. samtools flagstat的mapping record rate的计算方法

$$mapping record rate=mapped recorder number/total recorder number=((primary) mapped reads number + secondary mapped reads number)/(total reads number + secondary mapped reads number)$$

其中,recorder number代表sam文件中去除header部分的比对记录数量(每行一条比对记录,即行数)。

同一reads可能多次mapping,有多条记录,所以recorder number的数量会比reads number多。

  • mapped recorder number用的是50020312;
  • total recorder number用的是51231959;
  • secondary mapped reads number是12372427;

$$mapping record rate=50020312/51231959*100%=97.63%$$

有文章直接用mapping record rate,但建议用mapping rate来代表mapped reads的比例。

  1. 与hisat2的统计结果的不同
  • samtools flagstat的mapping record rate(97.63%)比hisat2的mapping rate(96.88%)高一些,原因在于计算方式的区别。
  1. 计算mapping rate
  • 通常我们在文章中使用reads的比例来代表mapping rate(即hisat2的计算方式),通过计算公式,可以利用samtools flagsta的统计数据计算mapping rate。

$$mapping rate = mapped reads number/total reads number = (mapped recorder number - secondary mapped reads number)/(total recorder number - secondary mapped reads number) = (50020312-12372427)/(51231959-12372427) = 37647885/38859532*100% = 96.88%$$

4. references

  1. hisat2和samtools flagstat计算的mapping rate不同的解释:https://zhuanlan.zhihu.com/p/73208822

  • 欢迎关注微信公众号:生信技工
  • 公众号主要分享生信分析、生信软件、基因组学、转录组学、植物进化、生物学概念等相关内容,包括生物信息学工具的基本原理、操作步骤和学习心得。
真诚赞赏,手留余香