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  1. ...with mate-pair reads followed by gap closure, was performed using Platanus v1.2.4 (Kajitani et al. 2014).Whole sequencing for a male whale shark used the 10x Genomics Chromium to produce Linked-Read data. A DNA library was prepared using 12 ng of gDNA extracted from blood cells according to the user guide...
  2. ...generated from the original clones, utilizing 85 specific oligonucleotide primers for gap closure and complete double-stranded coverage. The resulting sequences were edited to the established community standard of ≥99.99% accuracy. Of a total 1793 sequences obtained for this project, 122 reads (6.8%) were...
  3. ...in host–pathogen interactions (Adomako-Ankomah et al. 2016). In that initial study, we used sequence coverage to infer copy number, and we were eager to refine this analysis using the long-read de novo assemblies presented here.The gap closure enabled us to determine the number, order, and orientation...
  4. ...: 1682 – 1687 . Muzny, D.M., S. Richards, Y. Shen, and R.A. Gibbs.1994. PCR based strategies for gap closure in large-scale sequencing projects. In Automated DNA sequencing and analysis (ed. M.D. Adams, C. Fields, and J.C. Venter), pp. 182–190. Academic Press, San Diego, CA. Nagafuchi, S., , Yanagisawa...
  5. ...of gaps must still be closed by directed means. View larger version: In this window In a new window Figure 8. Probability of closure as a function of depth of coverage for various projects: 1. Zhu et al. (1999) ; 2. Dewar et al. (1998) ; 3. Fleischmann et al. (1995) ; 4. McPherson et al. (2001) ; 5. Adams...
  6. ...) 370, 373, 373A, or 377 sequencers. Sequence Assembly and Gap Closure Raw sequence data were transferred to a UNIX platform for editing and assembly. Vector and low-quality data were removed using SEQPREP software developed by the Molecular Biology Computational Resource Center at Baylor College...
  7. ...of sequenced clones. A tabulation of the number of gaps in a project as a function of overlap is provided in Table 1 . At infinite time (when a project has reached its jamming limit), the number of gaps decreases monotonically to zero as the allowed overlap increases from zero to fifty percent. If projects...
  8. ...end sequences. The average Phred ( Ewing and Green 1998 ; Ewing et al. 1998 ) quality score of the consensus contig sequence is 86.8, with 908,521 bp (91.3%) having the highest Phred Score of 90 and only 1198 bp (0.1%) having a Phred score <20. The total estimated length of the gaps is 15,143 bp...
  9. ...York, NY ), pp 73 – 89 . ↵ Richards S. , Muzny D.M. , Civitello D.M. , Lu F. , Gibbs R.A. Adams M. , Fields C. , Venter J. ( 1994 ) Sequence map gaps and directed reverse sequencing for the completion of large sequencing projects. in Automated DNA sequencing and analysis , eds Adams M. , Fields C...
  10. ...the Back End into the Front End to provide closure for gaps after initial shotgun sequencing has occurred (e.g., see Fleischmann et al. 1995 ). Significant strides have been made in all of these phases of the sequencing process. Increasingly, Front End steps are being automated by robotic systems ( Wilson...
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