NanoVar: accurate characterization of patients' genomic structural variants using low-depth nanopore...
NanoVar: accurate characterization of patients' genomic structural variants using low-depth nanopore sequencing
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Publisher
England: BioMed Central Ltd
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Language
English
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Publisher
England: BioMed Central Ltd
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Contents
The recent advent of third-generation sequencing technologies brings promise for better characterization of genomic structural variants by virtue of having longer reads. However, long-read applications are still constrained by their high sequencing error rates and low sequencing throughput. Here, we present NanoVar, an optimized structural variant...
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Full title
NanoVar: accurate characterization of patients' genomic structural variants using low-depth nanopore sequencing
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TN_cdi_doaj_primary_oai_doaj_org_article_34a655772a22470fb24f4fe43e3bcc5f
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_34a655772a22470fb24f4fe43e3bcc5f
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ISSN
1474-760X,1474-7596
E-ISSN
1474-760X
DOI
10.1186/s13059-020-01968-7
