Sequence assembly demystified

被引:283
作者
Nagarajan, Niranjan [1 ]
Pop, Mihai [2 ]
机构
[1] Genome Inst Singapore, Singapore 138672, Singapore
[2] Univ Maryland, Dept Comp Sci, College Pk, MD 20742 USA
基金
美国国家科学基金会;
关键词
DE-BRUIJN GRAPHS; RNA-SEQ DATA; QUASI-SPECIES RECONSTRUCTION; GENOME ASSEMBLIES; STRUCTURAL VARIATION; SINGLE-CELL; SHORT READS; BACTERIAL GENOMES; DRAFT ASSEMBLIES; RESTRICTION MAPS;
D O I
10.1038/nrg3367
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Advances in sequencing technologies and increased access to sequencing services have led to renewed interest in sequence and genome assembly. Concurrently, new applications for sequencing have emerged, including gene expression analysis, discovery of genomic variants and metagenomics, and each of these has different needs and challenges in terms of assembly. We survey the theoretical foundations that underlie modern assembly and highlight the options and practical trade-offs that need to be considered, focusing on how individual features address the needs of specific applications. We also review key software and the interplay between experimental design and efficacy of assembly.
引用
收藏
页码:157 / 167
页数:11
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