release 14.12.0 statistical software (Minitab Inc)
90
Structured Review
Minitab Inc
release 14.12.0 statistical software
Release 14.12.0 Statistical Software, supplied by Minitab Inc, 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/release+14%2E12%2E0+statistical+software/release+14+12+0+statistical+software/pm40377674-51-8-7
Average 90 stars, based on 1 article reviews
Release 14.12.0 Statistical Software, supplied by Minitab Inc, 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/release+14%2E12%2E0+statistical+software/release+14+12+0+statistical+software/pm40377674-51-8-7
Average 90 stars, based on 1 article reviews
release 14.12.0 statistical software - by Bioz Stars,
2026-09
90/100 stars
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Related Articles
Derivative Assay:Article Title: Hemoglobin Constant Spring among Southeast Asian Populations: Haplotypic Heterogeneities and Phylogenetic Analysis Article Snippet: Statistical analysis was performed using the Article Title: Genetic polymorphism of novel SNP rs5006884 in OR51B6 and SNP rs4499252 in AHSP among transfusion-dependent and non-transfusion-dependent β-thalassemia/Hb E patients in Thailand: a multivariate analysis of clinical and genetic polymorphism. Article Snippet: The multivariate models associated with genetic and clinical factors in compound heterozygous β-thalassemia and Hb E (n = 116) related to transfusion event (NTDT), and (TDT) was applied using multiple regression analysis on Article Title: Association Between Genetic Polymorphisms and Hb F Levels in Heterozygous β-Thalassemia 3.5 kb Deletions. Article Snippet: Single nucleotide polymorphisms (SNPs) in several genetic modifying factors have been related to Hb F levels, including c XmnI polymorphism, B-cell lymphoma/leukemia 11A (BCL11A), HBS1L-MYB intergenic polymorphism (HMIP) and a mutation in the Kr€ uppel-like factor 1 (KLF1).. This study aimed to determine whether genetic variability of these modifying factors affects Hb F levels in heterozygous b-thalassemia (b-thal) 3.5 kb deletion (NC_000011.10: g.5224302-5227791del13490bp).. A total of 111 b-thal 3.5 kb deletion carriers with Hb F levels ranging from 0.9 to 18.4% was recruited for this study. Article Title: Uniaxial and Multiaxial Fatigue Life Prediction of the Trabecular Bone Based on Physiological Loading: A Comparative Study. Article Snippet: Fatigue assessment of the trabecular bone has been developed to give a better understanding of bone properties.. While most fatigue studies are relying on uniaxial compressive load as the method of assessment, in various cases details are missing, or the uniaxial results are not very realistic.. In this paper, the effect of three different load histories from physiological loading applied on the trabecular bone were studied in order to predict the first failure surface and the fatigue lifetime. Article Title: Genetic polymorphism of novel SNP rs5006884 in OR51B6 and SNP rs4499252 in AHSP among transfusion-dependent and non-transfusion-dependent β-thalassemia/Hb E patients in Thailand: a multivariate analysis of clinical and genetic polymorphism. Article Snippet: Statistical analysis and proportion were performed using Article Title: A prospective controlled randomized multicenter study to evaluate the severity of compensatory sweating after one-stage bilateral thoracic sympathectomy versus unilateral thoracic sympathectomy in the dominant side Article Snippet: The sample size calculation for the two cases was carried out with the aid of Article Title: Genetic Background Studies of Eight Common Beta Thalassemia Mutations in Thailand Using β-Globin Gene Haplotype and Phylogenetic Analysis Article Snippet: The Fisher’s exact test revealed the derived allele frequency (DAF), and Article Title: The Validation of Whole β-Globin Gene Sequencing for Detecting β-Thalassemia Mutations Found in Thailand Using Next-Generation Sequencing (NGS). Article Snippet: Beta-thalassemia is an inherited disorder prevalent in thailand and southeast asia. several molecular techniques for identifying β-thalassemia mutations have been reported.. Next-generation sequencing (NGs) is a type of effective molecular testing with high throughput and accuracy. hence, this study aims to evaluate a novel barcode-tagged NGs approach based on a short-read assay. a total of 258 samples with 54 different β-thalassemia genotypes related to 32 mutations were gathered and evaluated. a library was constructed with the BtseqtM kit and sequencing was performed on the illumina NGs machine. the validation results showed 98.45% concordance with conventional genotypes. less discordant results (1.55%) were limited to insertional mutations and included one case of each of the following: HBB:c.27dupG, HBB:c.85dupc, HBB:c.216dupt, and HBB:c.440_441dupac.. Five single-nucleotide polymorphisms that derived from the NGs results were also analyzed in terms of allele frequency and revealed significant differences between the wild types and other β-genotypes. Software:Article Title: Hemoglobin Constant Spring among Southeast Asian Populations: Haplotypic Heterogeneities and Phylogenetic Analysis Article Snippet: Statistical analysis was performed using the Article Title: Genetic polymorphism of novel SNP rs5006884 in OR51B6 and SNP rs4499252 in AHSP among transfusion-dependent and non-transfusion-dependent β-thalassemia/Hb E patients in Thailand: a multivariate analysis of clinical and genetic polymorphism. Article Snippet: The multivariate models associated with genetic and clinical factors in compound heterozygous β-thalassemia and Hb E (n = 116) related to transfusion event (NTDT), and (TDT) was applied using multiple regression analysis on Article Title: Association Between Genetic Polymorphisms and Hb F Levels in Heterozygous β-Thalassemia 3.5 kb Deletions. Article Snippet: Single nucleotide polymorphisms (SNPs) in several genetic modifying factors have been related to Hb F levels, including c XmnI polymorphism, B-cell lymphoma/leukemia 11A (BCL11A), HBS1L-MYB intergenic polymorphism (HMIP) and a mutation in the Kr€ uppel-like factor 1 (KLF1).. This study aimed to determine whether genetic variability of these modifying factors affects Hb F levels in heterozygous b-thalassemia (b-thal) 3.5 kb deletion (NC_000011.10: g.5224302-5227791del13490bp).. A total of 111 b-thal 3.5 kb deletion carriers with Hb F levels ranging from 0.9 to 18.4% was recruited for this study. Article Title: Uniaxial and Multiaxial Fatigue Life Prediction of the Trabecular Bone Based on Physiological Loading: A Comparative Study. Article Snippet: Fatigue assessment of the trabecular bone has been developed to give a better understanding of bone properties.. While most fatigue studies are relying on uniaxial compressive load as the method of assessment, in various cases details are missing, or the uniaxial results are not very realistic.. In this paper, the effect of three different load histories from physiological loading applied on the trabecular bone were studied in order to predict the first failure surface and the fatigue lifetime. Article Title: Genetic polymorphism of novel SNP rs5006884 in OR51B6 and SNP rs4499252 in AHSP among transfusion-dependent and non-transfusion-dependent β-thalassemia/Hb E patients in Thailand: a multivariate analysis of clinical and genetic polymorphism. Article Snippet: Statistical analysis and proportion were performed using Article Title: A prospective controlled randomized multicenter study to evaluate the severity of compensatory sweating after one-stage bilateral thoracic sympathectomy versus unilateral thoracic sympathectomy in the dominant side Article Snippet: The sample size calculation for the two cases was carried out with the aid of Article Title: Genetic Background Studies of Eight Common Beta Thalassemia Mutations in Thailand Using β-Globin Gene Haplotype and Phylogenetic Analysis Article Snippet: The Fisher’s exact test revealed the derived allele frequency (DAF), and Article Title: The Validation of Whole β-Globin Gene Sequencing for Detecting β-Thalassemia Mutations Found in Thailand Using Next-Generation Sequencing (NGS). Article Snippet: Beta-thalassemia is an inherited disorder prevalent in thailand and southeast asia. several molecular techniques for identifying β-thalassemia mutations have been reported.. Next-generation sequencing (NGs) is a type of effective molecular testing with high throughput and accuracy. hence, this study aims to evaluate a novel barcode-tagged NGs approach based on a short-read assay. a total of 258 samples with 54 different β-thalassemia genotypes related to 32 mutations were gathered and evaluated. a library was constructed with the BtseqtM kit and sequencing was performed on the illumina NGs machine. the validation results showed 98.45% concordance with conventional genotypes. less discordant results (1.55%) were limited to insertional mutations and included one case of each of the following: HBB:c.27dupG, HBB:c.85dupc, HBB:c.216dupt, and HBB:c.440_441dupac.. Five single-nucleotide polymorphisms that derived from the NGs results were also analyzed in terms of allele frequency and revealed significant differences between the wild types and other β-genotypes. |