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Stepwise large genome assembly approach: a case of Siberian larch (Larix sibirica Ledeb).


ABSTRACT: BACKGROUND:De novo assembling of large genomes, such as in conifers (~?12-30 Gbp), which also consist of ~?80% of repetitive DNA, is a very complex and computationally intense endeavor. One of the main problems in assembling such genomes lays in computing limitations of nucleotide sequence assembly programs (DNA assemblers). As a rule, modern assemblers are usually designed to assemble genomes with a length not exceeding the length of the human genome (3.24 Gbp). Most assemblers cannot handle the amount of input sequence data required to provide sufficient coverage needed for a high-quality assembly. RESULTS:An original stepwise method of de novo assembly by parts (sets), which allows to bypass the limitations of modern assemblers associated with a huge amount of data being processed, is presented in this paper. The results of numerical assembling experiments conducted using the model plant Arabidopsis thaliana, Prunus persica (peach) and four most popular assemblers, ABySS, SOAPdenovo, SPAdes, and CLC Assembly Cell, showed the validity and effectiveness of the proposed stepwise assembling method. CONCLUSION:Using the new stepwise de novo assembling method presented in the paper, the genome of Siberian larch, Larix sibirica Ledeb. (12.34 Gbp) was completely assembled de novo by the CLC Assembly Cell assembler. It is the first genome assembly for larch species in addition to only five other conifer genomes sequenced and assembled for Picea abies, Picea glauca, Pinus taeda, Pinus lambertiana, and Pseudotsuga menziesii var. menziesii.

SUBMITTER: Kuzmin DA 

PROVIDER: S-EPMC6362582 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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Stepwise large genome assembly approach: a case of Siberian larch (Larix sibirica Ledeb).

Kuzmin Dmitry A DA   Feranchuk Sergey I SI   Sharov Vadim V VV   Cybin Alexander N AN   Makolov Stepan V SV   Putintseva Yuliya A YA   Oreshkova Natalya V NV   Krutovsky Konstantin V KV  

BMC bioinformatics 20190205 Suppl 1


<h4>Background</h4>De novo assembling of large genomes, such as in conifers (~ 12-30 Gbp), which also consist of ~ 80% of repetitive DNA, is a very complex and computationally intense endeavor. One of the main problems in assembling such genomes lays in computing limitations of nucleotide sequence assembly programs (DNA assemblers). As a rule, modern assemblers are usually designed to assemble genomes with a length not exceeding the length of the human genome (3.24 Gbp). Most assemblers cannot h  ...[more]

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