Evaluating nanopore sequencing data processing pipelines for structural variation identification
Abstract Background Structural variations (SVs) account for about 1% of the differences among human genomes and play a significant role in phenotypic variation and disease susceptibility. The emerging nanopore sequencing technology can generate long sequence reads and can potentially provide accurat...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2019-11-01
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Series: | Genome Biology |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13059-019-1858-1 |