Deciphering complex genome rearrangements in C. elegans using short-read whole genome sequencing
Deciphering complex genome rearrangements in C. elegans using short-read whole genome sequencing
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London: Nature Publishing Group UK
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English
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London: Nature Publishing Group UK
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Genomic rearrangements cause congenital disorders, cancer, and complex diseases in human. Yet, they are still understudied in rare diseases because their detection is challenging, despite the advent of whole genome sequencing (WGS) technologies. Short-read (srWGS) and long-read WGS approaches are regularly compared, and the latter is commonly recom...
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Deciphering complex genome rearrangements in C. elegans using short-read whole genome sequencing
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TN_cdi_doaj_primary_oai_doaj_org_article_cc2274dbe4434c73b2ead9382c12c03a
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_cc2274dbe4434c73b2ead9382c12c03a
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ISSN
2045-2322
E-ISSN
2045-2322
DOI
10.1038/s41598-021-97764-9
