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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Genomics Inform
Egile Nagusiak: Lee, Yuna, Park, Kiejung, Koh, Insong
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Korea Genome Organization 2019
Gaiak:
Sarrera elektronikoa: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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