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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. Three principal changes were simultaneously made and applied to the assembly of the mouse genome, during a six-month period of development: (1) Supercontigs (scaffolds) were iteratively broken and rejoined using several criteria, yielding a 64-fold increase in length (N50), and apparent elimination of all global misjoins; (2) gaps between contigs in supercontigs were filled (partially or completely) by insertion of reads, as suggested by pairing within the supercontig, increasing the N50 contig length by 50%; (3) memory usage was reduced fourfold. The outcome of this mouse assembly and its analysis are described in (Mouse Genome Sequencing Consortium 2002).
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David B. Jaffe
Jonathan A. Butler
Sante Gnerre
Genome Research
Massachusetts Institute of Technology
Whitehead Institute for Biomedical Research
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Jaffe et al. (Wed,) studied this question.
www.synapsesocial.com/papers/6a08cab42a35bb5cdfba0389 — DOI: https://doi.org/10.1101/gr.828403
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