Cargando…
Detection of trait-associated structural variations using short-read sequencing
Genomic structural variation (SV) affects genetic and phenotypic characteristics in diverse organisms, but the lack of reliable methods to detect SV has hindered genetic analysis. We developed a computational algorithm (MOPline) that includes missing call recovery combined with high-confidence SV ca...
Autores principales: | Kosugi, Shunichi, Kamatani, Yoichiro, Harada, Katsutoshi, Tomizuka, Kohei, Momozawa, Yukihide, Morisaki, Takayuki, Terao, Chikashi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10300613/ https://www.ncbi.nlm.nih.gov/pubmed/37388916 http://dx.doi.org/10.1016/j.xgen.2023.100328 |
Ejemplares similares
-
Comprehensive evaluation of structural variation detection algorithms for whole genome sequencing
por: Kosugi, Shunichi, et al.
Publicado: (2019) -
Susceptibility loci and polygenic architecture highlight population specific and common genetic features in inguinal hernias: genetics in inguinal hernias
por: Hikino, Keiko, et al.
Publicado: (2021) -
Federated analysis of BRCA1 and BRCA2 variation in a Japanese cohort
por: Casaletto, James, et al.
Publicado: (2022) -
A novel intragenic deletion in OPHN1 in a Japanese patient with Dandy-Walker malformation
por: Iida, Aritoshi, et al.
Publicado: (2018) -
Genome-wide association study reveals BET1L associated with survival time in the 137,693 Japanese individuals
por: Akiyama, Masato, et al.
Publicado: (2023)