Using linkage maps to correct and scaffold de novo genome assemblies: methods, challenges, and computational tools

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Date
2015
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Volume Title
Publisher
Frontiers
Abstract

Modern high-throughput DNA sequencing has made it possible to inexpensively produce genome sequences, but in practice many of these draft genomes are fragmented and incomplete. Genetic linkage maps based on recombination rates between physical markers have been used in biology for over 100 years and a linkage map, when paired with a de novo sequencing project, can resolve mis-assemblies and anchor chromosome-scale sequences. Here, I summarize the methodology behind integrating de novo assemblies and genetic linkage maps, outline the current challenges, review the available software tools, and discuss new mapping technologies.

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Keywords
FACTOR-BASED VECTOR, GENETIC MAPS, IN-VITRO, CHROMATIN INTERACTIONS, RECOMBINANT INBREDS, MICROBIAL GENOMES, HUMAN DNA, SHOTGUN, CONSTRUCTION, DROSOPHILA, Genetics & Heredity
Citation
Fierst, J. L. (2015). Using linkage maps to correct and scaffold de novo genome assemblies: methods, challenges, and computational tools. In Frontiers in Genetics (Vol. 6). Frontiers Media SA. https://doi.org/10.3389/fgene.2015.00220