De Novo assembly and genomic structural variation analysis with genome sequencer FLX 3K long-tag paired end reads

BioTechniques

Volumn 44, Issue 6, 2008, Pages 829-831

  Jarvie, Thomas ^a   Harkins, Timothy ^b  

^a 454 Life Sciences ^*  (United States)

^b Roche Diagnostics Corporation   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA FRAGMENT; GENOMIC DNA;

ARTICLE; DNA LIBRARY; DNA SEQUENCE; GENE SEQUENCE; GENE STRUCTURE; GENETIC ANALYSIS; GENETIC VARIABILITY; HUMAN; HYDRODYNAMICS; METHYLATION; NEBULIZATION; PHENOTYPIC VARIATION;

BASE SEQUENCE; CHROMOSOME MAPPING; DNA MUTATIONAL ANALYSIS; EXPRESSED SEQUENCE TAGS; GENETIC MARKERS; MOLECULAR SEQUENCE DATA; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, DNA; VARIATION (GENETICS);

EID: 45249108310     PISSN: 07366205     EISSN: None     Source Type: Journal    
DOI: 10.2144/000112894     Document Type: Article

References (1)

1. Korbel, J.O., A.E. Urban, J.P. Affourtit, B. Godwin, F. Grubert, J.F. Simons, P.M. Kim, D. Palejev, N.J. Carriero, L Du, B.E. Taillon, Z. Chen, A. Tanzer, A.C.E. Saunders, J. Chi, F. Yang, N.P. Carter, M.E. Hurles, S.M. Weissman, T.T. Harkins, M.B. Gerstein, M. Egholm, and M. Snyder. Paired-End Mapping Reveals Extensive Structural Variation in the Human Genome. (2007) Science 318(5849):420-426.