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Volumn 15, Issue , 2014, Pages

Reference-free SNP detection: Dealing with the data deluge

Author keywords

[No Author keywords available]

Indexed keywords

DNA STRUCTURE; GENETIC VARIATION; HUMAN; HUMAN TISSUE; MEDICINE; METAGENOMICS; MODEL; SCIENTIST; SINGLE NUCLEOTIDE POLYMORPHISM; STORAGE; ANIMAL; CONTIG MAPPING; GENETIC VARIABILITY; THEORETICAL MODEL;

EID: 84925282722     PISSN: None     EISSN: 14712164     Source Type: Journal    
DOI: 10.1186/1471-2164-15-S4-S10     Document Type: Review
Times cited : (26)

References (22)
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    • Prism: Pair-read informed split-read mapping for base-pair level detection of insertion, deletion and structural variants
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    • Computational methods for discovering structural variation with next-generation sequencing
    • Medvedev P, Stanciu M, Brudno M: Computational methods for discovering structural variation with next-generation sequencing. Nature Methods 2009, 6(11s):13-20.
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    • De novo assembly and genotyping of variants using colored de Bruijn graphs
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    • (2012) Nature Genetics , vol.44 , Issue.2 , pp. 226-232
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    • Reference-free SNP calling: improved accuracy by preventing incorrect calls from repetitive genomic regions
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.