Literature DB >> 8808467

Random subcloning.

J C Roach1.   

Abstract

Random subcloning strategies are commonly employed for analyzing pieces of DNA that are too large for direct analysis. Such strategies are applicable to gene finding, physical mapping, and DNA sequencing. Random subcloning refers to the generation of many small, directly analyzable fragments of DNA that represent random fragments of a larger whole, such as a genome. Following analysis of these fragments, a map or sequence of the original target may be reconstructed. Mathematical modeling is useful in planning such strategies and in providing a reference for their evaluation, both during execution and following completion. The statistical theory necessary for constructing these models has been developed independently over the last century. This paper brings this theory together into a statistical model for random subcloning strategies. This mathematical model retains its utility even at high subclone redundancies, which are necessary for project completion. The discussion here centers on shotgun sequencing, a random subcloning strategy envisioned as the method of choice for sequencing the human genome.

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Year:  1995        PMID: 8808467     DOI: 10.1101/gr.5.5.464

Source DB:  PubMed          Journal:  Genome Res        ISSN: 1088-9051            Impact factor:   9.043


  9 in total

1.  Theories and applications for sequencing randomly selected clones.

Authors:  M C Wendl; M A Marra; L W Hillier; A T Chinwalla; R K Wilson; R H Waterston
Journal:  Genome Res       Date:  2001-02       Impact factor: 9.043

2.  Parking strategies for genome sequencing.

Authors:  J C Roach; V Thorsson; A F Siegel
Journal:  Genome Res       Date:  2000-07       Impact factor: 9.043

3.  Generalized gap model for bacterial artificial chromosome clone fingerprint mapping and shotgun sequencing.

Authors:  Michael C Wendl; Robert H Waterston
Journal:  Genome Res       Date:  2002-12       Impact factor: 9.043

4.  Coverage theories for metagenomic DNA sequencing based on a generalization of Stevens' theorem.

Authors:  Michael C Wendl; Karthik Kota; George M Weinstock; Makedonka Mitreva
Journal:  J Math Biol       Date:  2012-09-11       Impact factor: 2.259

5.  Extension of Lander-Waterman theory for sequencing filtered DNA libraries.

Authors:  Michael C Wendl; W Brad Barbazuk
Journal:  BMC Bioinformatics       Date:  2005-10-10       Impact factor: 3.169

6.  Bounds on the distribution of the number of gaps when circles and lines are covered by fragments: theory and practical application to genomic and metagenomic projects.

Authors:  John Moriarty; Julian R Marchesi; Anthony Metcalfe
Journal:  BMC Bioinformatics       Date:  2007-03-02       Impact factor: 3.169

7.  Whole-genome haplotyping approaches and genomic medicine.

Authors:  Gustavo Glusman; Hannah C Cox; Jared C Roach
Journal:  Genome Med       Date:  2014-09-25       Impact factor: 11.117

8.  Probabilistic model based on circular statistics for quantifying coverage depth dynamics originating from DNA replication.

Authors:  Shinya Suzuki; Takuji Yamada
Journal:  PeerJ       Date:  2020-03-27       Impact factor: 2.984

9.  Low-pass sequencing for microbial comparative genomics.

Authors:  Young Ah Goo; Jared Roach; Gustavo Glusman; Nitin S Baliga; Kerry Deutsch; Min Pan; Sean Kennedy; Shiladitya DasSarma; Wailap Victor Ng; Leroy Hood
Journal:  BMC Genomics       Date:  2004-01-12       Impact factor: 3.969

  9 in total

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