Yukuto Sato

发表

Estimating copy numbers of alleles from population-scale high-throughput sequencing data

Masao Nagasaki, Kaname Kojima, Naoki Nariai, 2015, BMC Bioinformatics.

A statistical variant calling approach from pedigree information and local haplotyping with phase informative reads

Masao Nagasaki, Kaname Kojima, Naoki Nariai, 2013, Bioinform..

Evolution of multiple phosphodiesterase isoforms in stickleback involved in cAMP signal transduction pathway

Yukuto Sato, Yasuyuki Hashiguchi, Mutsumi Nishida, 2009, BMC Systems Biology.

SVEM: A Structural Variant Estimation Method Using Multi-mapped Reads on Breakpoints

Masao Nagasaki, Tetsuo Shibuya, Kaname Kojima, 2014, AlCoB.

iSVP: an integrated structural variant calling pipeline from high-throughput sequencing data

Akira Ono, Masao Nagasaki, Kaname Kojima, 2013, BMC Systems Biology.

HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data

Masao Nagasaki, Kaname Kojima, Naoki Nariai, 2015, BMC Genomics.

HapMonster: A Statistically Unified Approach for Variant Calling and Haplotyping Based on Phase-Informative Reads

Masao Nagasaki, Kaname Kojima, Naoki Nariai, 2014, AlCoB.

MitoFish and MiFish Pipeline: A Mitochondrial Genome Database of Fish with an Analysis Pipeline for Environmental DNA Metabarcoding

Tsukasa Fukunaga, Wataru Iwasaki, Yukuto Sato, 2018, Molecular biology and evolution.

Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals

Kengo Kinoshita, Masao Nagasaki, Naoki Nariai, 2015, Nature Communications.

iJGVD: an integrative Japanese genome variation database based on whole-genome sequencing

Masao Nagasaki, Naoki Nariai, Fumiki Katsuoka, 2015, Human Genome Variation.

Rapid genome reshaping by multiple-gene loss after whole-genome duplication in teleost fish suggested by mathematical modeling

Katsumi Tsukamoto, Yukuto Sato, Jun G. Inoue, 2015, Proceedings of the National Academy of Sciences.

TIGAR2: sensitive and accurate estimation of transcript isoform expression with longer RNA-Seq reads

Masao Nagasaki, Naoki Nariai, Takahiro Mimori, 2014, BMC Genomics.