4.7 Article

Breed-specific reference sequence optimized mapping accuracy of NGS analyses for pigs

期刊

BMC GENOMICS
卷 22, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12864-021-08030-1

关键词

Mitochondrial genome; Mapping; Reference sequence; SNP calling; Pig

资金

  1. National Natural Science Foundation of China-Deutsche Forschungsgemeinschaft [31961133031]
  2. National Natural Science Foundation of China [32102526, 32002172]
  3. China Postdoctoral Science Foundation [2020M682217]
  4. Shandong Provincial Postdoctoral Program for Innovative Talent
  5. Shandong Provincial Natural Science Foundation [ZR2020QC176, ZR2020QC175]

向作者/读者索取更多资源

This study compared the accuracy of mitogenome alignment and SNP calling using three different types of reference sequences for mitochondrial DNA analyses. The results showed that breed-specific reference sequences were optimal for mitogenome analyses, providing a refined processing perspective for NGS data.
Background Reference sequences play a vital role in next-generation sequencing (NGS), impacting mapping quality during genome analyses. However, reference genomes usually do not represent the full range of genetic diversity of a species as a result of geographical divergence and independent demographic events of different populations. For the mitochondrial genome (mitogenome), which occurs in high copy numbers in cells and is strictly maternally inherited, an optimal reference sequence has the potential to make mitogenome alignment both more accurate and more efficient. In this study, we used three different types of reference sequences for mitogenome mapping, i.e., the commonly used reference sequence (CU-ref), the breed-specific reference sequence (BS-ref) and the sample-specific reference sequence (SS-ref), respectively, and compared the accuracy of mitogenome alignment and SNP calling among them, for the purpose of proposing the optimal reference sequence for mitochondrial DNA (mtDNA) analyses of specific populations Results Four pigs, representing three different breeds, were high-throughput sequenced, subsequently mapping reads to the reference sequences mentioned above, resulting in a largest mapping ratio and a deepest coverage without increased running time when aligning reads to a BS-ref. Next, single nucleotide polymorphism (SNP) calling was carried out by 18 detection strategies with the three tools SAMtools, VarScan and GATK with different parameters, using the bam results mapping to BS-ref. The results showed that all eighteen strategies achieved the same high specificity and sensitivity, which suggested a high accuracy of mitogenome alignment by the BS-ref because of a low requirement for SNP calling tools and parameter choices. Conclusions This study showed that different reference sequences representing different genetic relationships to sample reads influenced mitogenome alignment, with the breed-specific reference sequences being optimal for mitogenome analyses, which provides a refined processing perspective for NGS data.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据