A method for finding single-nucleotide polymorphisms with allele frequencies is sequences of deep coverage

BMC Bioinformatics

Volumn 6, Issue , 2005, Pages

  Wang, Jianmin ^a   Huang, Xiaoqiu ^a  

^a Iowa State University   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EXPRESSED SEQUENCE TAGS; GENOME SEQUENCES; MULTIPLE SEQUENCE ALIGNMENTS; OPTIMAL SUBSETS; PAIRWISE ALIGNMENT; SINGLE NUCLEOTIDE POLYMORPHISMS;

COMPUTATIONAL METHODS;

GENES;

ARTICLE; BIOINFORMATICS; COMPUTER ANALYSIS; COMPUTER PROGRAM; CONTROLLED STUDY; DNA SEQUENCE; EXPRESSED SEQUENCE TAG; GENE FREQUENCY; HUMAN; INFORMATION PROCESSING; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; GENETICS; INFORMATION RETRIEVAL; MOLECULAR COMPUTER; PROCEDURES; SEQUENCE ALIGNMENT;

COMPUTERS, MOLECULAR; EXPRESSED SEQUENCE TAGS; GENE FREQUENCY; HUMANS; INFORMATION STORAGE AND RETRIEVAL; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ALIGNMENT; SOFTWARE;

EID: 25444532272     PISSN: 14712105     EISSN: 14712105     Source Type: Journal    
DOI: 10.1186/1471-2105-6-220     Document Type: Article

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