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...

Полное описание

Сохранить в:
Библиографические подробности
Опубликовано в: :Bioinformatics
Главные авторы: Kavak, Pınar, Lin, Yen-Yi, Numanagić, Ibrahim, Asghari, Hossein, Güngör, Tunga, Alkan, Can, Hach, Faraz
Формат: Artigo
Язык:Inglês
Опубликовано: Oxford University Press 2017
Предметы:
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
Online-ссылка: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
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы