Considerations for initiating a wildlife genomics research project in south and south-east Asia
Next-generation sequencing (NGS) based genomic studies are revolutionizing the field of
wildlife biology. These methods have yielded unprecedented insights for understanding …
wildlife biology. These methods have yielded unprecedented insights for understanding …
New perspectives on the genetic structure of dotted gizzard shad (Konosirus punctatus) based on RAD-seq
Y Peng, Y Liu, J Li, K Zhang, X Jin, S Zheng… - Marine Life Science & …, 2024 - Springer
To maintain, develop and rationally utilize marine organisms, understanding their genetic
structure and habitat adaptation pattern is necessary. Konosirus punctatus, which is a …
structure and habitat adaptation pattern is necessary. Konosirus punctatus, which is a …
Acceleration of BAM I/O on distributed file systems
S Ito, S Miyano, K Ono - 2023 IEEE International Conference on …, 2023 - ieeexplore.ieee.org
Rapid advances in high-throughput sequencers have made it possible to obtain large
amounts of whole genome data quickly and inexpensively. As the amount of data increases …
amounts of whole genome data quickly and inexpensively. As the amount of data increases …
Large-scaleWGS Analysis on the supercomputer Fugaku
S Ito, K Ono, S Miyano - Proceedings of the 2024 14th International …, 2024 - dl.acm.org
The remarkable improvement in the performance of next-generation sequencers has led to
the analysis of large numbers of samples in recent years for whole-genome analysis. The …
the analysis of large numbers of samples in recent years for whole-genome analysis. The …
An investigation into the genetic basis of autosomal recessive Osteogenesis imperfecta (OI) III in a South African family of mixed ancestry
SA Fernol - 2022 - etd.uwc.ac.za
Osteogenesis Imperfecta (OI) is a rare skeletal dysplasia that is primarily characterized by
bone fragility, recurrent fractures, and bone deformities. Over the years there has been an …
bone fragility, recurrent fractures, and bone deformities. Over the years there has been an …
Whole-Exome Data Analysis: Detection of Candidate Gene Mutations for Mitochondrial Encephalohepatopathy
Mitochondrial Encephalohepatopathy (MEH) is an autosomal recessive
neurodevelopmental disorder usually accompanied by microcephaly, white matter changes …
neurodevelopmental disorder usually accompanied by microcephaly, white matter changes …