Variant genotyping with gap filling

Author:

Walve Riku,Salmela LeenaORCID,Mäkinen Veli

Funder

Academy of Finland

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference15 articles.

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4. ABySS: a parallel assembler for short read sequence data;JT Simpson;Genome Res,2009

5. SOAPdenovo2: an empirically improved memory-efficient short-read de novo assembler;R Luo;GigaScience,2012

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. A machine learning framework for genotyping the structural variations with copy number variant;BMC Medical Genomics;2020-08

2. Safely Filling Gaps with Partial Solutions Common to All Solutions;IEEE/ACM Transactions on Computational Biology and Bioinformatics;2019-03-01

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