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2,570
ARACHNE: a whole-genome shotgun assembler
- Genome Res
, 2002
"... We describe a new computer system, called ARACHNE, for assembling genome sequence using paired-end whole-genome shotgun reads. ARACHNE has several key features, including an efficient and sensitive procedure for finding read overlaps, a procedure for scoring overlaps that achieves high accuracy by c ..."
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Cited by 177 (7 self)
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We describe a new computer system, called ARACHNE, for assembling genome sequence using paired-end whole-genome shotgun reads. ARACHNE has several key features, including an efficient and sensitive procedure for finding read overlaps, a procedure for scoring overlaps that achieves high accuracy
Whole-Genome Sequence Assembly for Mammalian Genomes: Arachne 2
"... We previously described the whole-genome assembly program Arachne, presenting assemblies of simulated data for small to mid-sized genomes. Here we describe algorithmic adaptations to the program, allowing for assembly of mammalian-size genomes, and also improving the assembly of smaller genomes. Thr ..."
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Cited by 68 (2 self)
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are described in (Mouse Genome Sequencing Consortium 2002). In the whole-genome shotgun method of genome sequencing, as presently practiced, the entire genome is sheared to specified approximate sizes (generally chosen from the range 2–200 kb), yielding random fragments (called inserts), whose ends can
Assembly of protein tertiary structures from fragments with similar local sequences using simulated annealing and Bayesian scoring functions
- J. MOL. BIOL
, 1997
"... We explore the ability of a simple simulated annealing procedure to assemble native-like structures from fragments of unrelated protein structures with similar local sequences using Bayesian scoring functions. Environment and residue pair specific contributions to the scoring functions appear as the ..."
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Cited by 393 (70 self)
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We explore the ability of a simple simulated annealing procedure to assemble native-like structures from fragments of unrelated protein structures with similar local sequences using Bayesian scoring functions. Environment and residue pair specific contributions to the scoring functions appear
Whole-genome sequencing and assembly with highthroughput, short read technologies
- PLoS ONE
, 2007
"... While recently developed short-read sequencing technologies may dramatically reduce the sequencing cost and eventually achieve the $1000 goal for re-sequencing, their limitations prevent the de novo sequencing of eukaryotic genomes with the standard shotgun sequencing protocol. We present SHRAP (SHo ..."
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Cited by 24 (1 self)
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. melanogaster and the entire human genome, our clone-ordering method produces accurate maps, thereby localizing fragment assembly and enabling the parallelization of the subsequent steps of our pipeline. Thus, we have demonstrated that truly inexpensive de novo sequencing of mammalian
Research Heterochromatic sequences in a Drosophila whole-genome shotgun assembly
, 2002
"... Background: Most eukaryotic genomes include a substantial repeat-rich fraction termed heterochromatin, which is concentrated in centric and telomeric regions. The repetitive nature of heterochromatic sequence makes it difficult to assemble and analyze. To better understand the heterochromatic compon ..."
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component of the Drosophila melanogaster genome, we characterized and annotated portions of a whole-genome shotgun sequence assembly. Results: WGS3, an improved whole-genome shotgun assembly, includes 20.7 Mb of draft-quality sequence not represented in the Release 3 sequence spanning the euchromatin. We
Whole-Genome Sequencing: Ready
"... Rapid technological advances in DNA sequencing are facilitating the perception that whole-genome sequencing (WGS) will soon be available as a routine clinical diagnostic—and predictive—test. Current clinical testing is typically diagnostic, focusing on sin-gle genes or small gene panels, identifying ..."
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Rapid technological advances in DNA sequencing are facilitating the perception that whole-genome sequencing (WGS) will soon be available as a routine clinical diagnostic—and predictive—test. Current clinical testing is typically diagnostic, focusing on sin-gle genes or small gene panels
Human whole-genome shotgun sequencing
- Genome Research
, 1997
"... Large-scale sequencing of the human genome is now under way (Boguski et al. 1996; Marshall and Pennisi 1996). Although at the beginning of the Genome Project, many doubted the scientific value of sequencing the entire human genome, these doubts have evaporated almost entirely (Gibbs 1995; Olson 1995 ..."
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Cited by 40 (2 self)
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Escherichia coli clones, followed by complete sequencing of these clones one at a time. In this article, we outline an alternative approach to sequencing the human and other large genomes, which we argue is less costly and more informative than the clone-by-clone approach. A Plan for Human Whole-Genome
Whole-genome validation of high-information-content fingerprinting
- Plant Physiol
, 2005
"... Fluorescent-based high-information-content fingerprinting (HICF) techniques have recently been developed for physical mapping. These techniques make use of automated capillary DNA sequencing instruments to enable both high-resolution and high-throughput fingerprinting. In this article, we report the ..."
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Cited by 10 (1 self)
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as previously used for the whole-genome agarose FPC map, providing a unique opportunity for direct comparison of the agarose and HICF methods; as a result, it was found that HICF has substantially greater sensitivity in forming contigs. An improved assembly procedure is also described that uses automatic end
Sequencing technologies - the next generation.
- Nature Reviews
, 2010
"... Abstract | Demand has never been greater for revolutionary technologies that deliver fast, inexpensive and accurate genome information. This challenge has catalysed the development of next-generation sequencing (NGS) technologies. The inexpensive production of large volumes of sequence data is the ..."
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Cited by 286 (2 self)
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is the primary advantage over conventional methods. Here, I present a technical review of template preparation, sequencing and imaging, genome alignment and assembly approaches, and recent advances in current and near-term commercially available NGS instruments. I also outline the broad range of applications
Bioinformatics Whole-Genome Validation of High-Information-Content
"... Fluorescent-based high-information-content fingerprinting (HICF) techniques have recently been developed for physical mapping. These techniques make use of automated capillary DNA sequencing instruments to enable both high-resolution and high-throughput fingerprinting. In this article, we report the ..."
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as previously used for the whole-genome agarose FPC map, providing a unique opportunity for direct comparison of the agarose and HICF methods; as a result, it was found that HICF has substantially greater sensitivity in forming contigs. An improved assembly procedure is also described that uses automatic end
Results 1 - 10
of
2,570