genetic analysis (StaGen Co Ltd)
90
Structured Review
StaGen Co Ltd
genetic analysis
Genetic Analysis, supplied by StaGen Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/next-generation+sequencing+data+analysis/next+generation+sequencing+data+processing/pm30810208-218-8-16
Average 90 stars, based on 1 article reviews
Genetic Analysis, supplied by StaGen Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/next-generation+sequencing+data+analysis/next+generation+sequencing+data+processing/pm30810208-218-8-16
Average 90 stars, based on 1 article reviews
genetic analysis - by Bioz Stars,
2026-09
90/100 stars
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other:Article Title: Genome-wide association meta-analysis and Mendelian randomization analysis confirm the influence of ALDH2 on sleep durationin the Japanese population. Article Snippet: We appreciate their support on genetic analysis from Article Title: Association of primary ovarian insufficiency with a specific human leukocyte antigen haplotype (A*24:02-C*03:03-B*35:01) in Japanese women. Article Snippet: Primary ovarian insufficiency (POI) is a heterogeneous condition defined by the triad of oligo/amenorrhea, elevated gonadotropins and estrogen deficiency in women under the age of 40 years.. Although autoimmune abnormalities appear to be involved in the development of POI, there are only a few studies with respect to human leukocyte antigen (HLA).. The objective of this study was to identify an HLA allele(s) and/or haplotype(s) constituting a susceptibility factor(s) for POI. Sequencing:Article Title: Whole-exome sequencing reveals the genetic causes and modifiers of moyamoya syndrome. Article Snippet: .. We thank the DNA donors and the supporting medical staff for their contribution, Makiko Terada (Institute for Comprehensive Medical Sciences, Tokyo Women’s Medical University, Tokyo, Japan) for providing technical assistance, and Mitsuhiro Amemiya and Next-Generation Sequencing:Article Title: Deletion in the Cobalamin Synthetase W Domain–Containing Protein 1 Gene Is associated with Congenital Anomalies of the Kidney and Urinary Tract Article Snippet: .. We also thank |