Discovery and genotyping of novel sequence insertions in many sequenced individuals

MOTIVATION: Despite recent advances in algorithms design to characterize structural variation using high-throughput short read sequencing (HTS) data, characterization of novel sequence insertions longer than the average read length remains a challenging task. This is mainly due to both computational...

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Detalhes bibliográficos
Publicado no:Bioinformatics
Main Authors: Kavak, Pınar, Lin, Yen-Yi, Numanagić, Ibrahim, Asghari, Hossein, Güngör, Tunga, Alkan, Can, Hach, Faraz
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2017
Assuntos:
Ismb/Eccb 2017: The 25th Annual Conference Intelligent Systems for Molecular Biology Held Jointly with the 16th Annual European Conference on Computational Biology, Prague, Czech Republic, July 21–25, 2017
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5870608/
https://ncbi.nlm.nih.gov/pubmed/28881988
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btx254
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