EAGLE: Explicit Alternative Genome Likelihood Evaluator
Abstract Background Reliable detection of genome variations, especially insertions and deletions (indels), from single sample DNA sequencing data remains challenging, partially due to the inherent uncertainty involved in aligning sequencing reads to the reference genome. In practice a variety of ad...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2018-04-01
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Series: | BMC Medical Genomics |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s12920-018-0342-1 |