作者: Gabor T. Marth , Ian Korf , Mark D. Yandell , Raymond T. Yeh , Zhijie Gu
DOI: 10.1038/70570
关键词: Reference genome 、 Expressed sequence tag 、 Biology 、 Nucleic acid sequence 、 Sequence alignment 、 Genetic marker 、 Multiple sequence alignment 、 Genetics 、 Computational biology 、 Sequence (medicine) 、 Alignment-free sequence analysis
摘要: Single-nucleotide polymorphisms (SNPs) are the most abundant form of human genetic variation and a resource for mapping complex genetic traits 1. The large volume of data …