Publisher
Springer Science and Business Media LLC
Reference36 articles.
1. Li, H. Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM. Preprint at
https://arxiv.org/abs/1303.3997
(2013).
2. DePristo, M. A. et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat. Genet. 43, 491–498 (2011).
3. Rimmer, A. et al. Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications. Nat. Genet. 46, 912–918 (2014).
4. 1000 Genomes Project Consortium. A global reference for human genetic variation. Nature 526, 68–74 (2015).
5. Sudmant, P. H. et al. An integrated map of structural variation in 2,504 human genomes. Nature 526, 75–81 (2015).
Cited by
62 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献