Fast and accurate read alignment for resequencing
Author(s) -
John C. Mu,
Hui Jiang,
Amirhossein Kiani,
Marghoob Mohiyuddin,
Narges Bani Asadi,
Wing Hung Wong
Publication year - 2012
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/bts450
Subject(s) - computer science , indel , workflow , task (project management) , reference genome , alignment free sequence analysis , key (lock) , sequence (biology) , sequence alignment , multiple sequence alignment , dna sequencing , data mining , operating system , genetics , biology , database , gene , management , peptide sequence , genotype , single nucleotide polymorphism , economics
Next-generation sequence analysis has become an important task both in laboratory and clinical settings. A key stage in the majority sequence analysis workflows, such as resequencing, is the alignment of genomic reads to a reference genome. The accurate alignment of reads with large indels is a computationally challenging task for researchers.
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