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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Detalles Bibliográficos
Autores principales: Lee, Yuna, Park, Kiejung, Koh, Insong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korea Genome Organization 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944045/
https://www.ncbi.nlm.nih.gov/pubmed/31896240
http://dx.doi.org/10.5808/GI.2019.17.4.e40

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944045/
https://www.ncbi.nlm.nih.gov/pubmed/31896240
http://dx.doi.org/10.5808/GI.2019.17.4.e40

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