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Analysis of unmapped regions associated with long deletions in Korean whole genome sequences based on short read data
While studies aimed at detecting and analyzing indels or single nucleotide polymorphisms within human genomic sequences have been actively conducted, studies on detecting long insertions/deletions are not easy to orchestrate. For the last 10 years, the availability of long read data of human genomes...
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| Publicat a: | Genomics Inform |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Korea Genome Organization
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6944045/ https://ncbi.nlm.nih.gov/pubmed/31896240 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5808/GI.2019.17.4.e40 |
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