geneious version 10.2.3 (Biomatters Ltd)
90
Structured Review
Biomatters Ltd
geneious version 10.2.3
Geneious Version 10.2.3, supplied by Biomatters 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/geneious+version+10%2E2%2E3/geneious+software/pmc12258190-28-15-18
Average 90 stars, based on 1 article reviews
Geneious Version 10.2.3, supplied by Biomatters 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/geneious+version+10%2E2%2E3/geneious+software/pmc12258190-28-15-18
Average 90 stars, based on 1 article reviews
geneious version 10.2.3 - by Bioz Stars,
2026-09
90/100 stars
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other:Article Title: The complete chloroplast genome of oriental false hawksbeard Youngia japonica (Asteraceae, tribe Cichorieae) Article Snippet: The complete chloroplast genome of Y. japonica was finally generated and then annotated using the Article Title: Potential role of heteroplasmic mitochondrial DNA mutations in modulating the subtype-specific adaptation of oral squamous cell carcinoma to cisplatin therapy Article Snippet: The mapping statistics were generated using QualiMap [ ] and Geneious version 10.2.3 ( Article Title: Detection and molecular characterization of chicken parvovirus and chicken megrivirus in layer breeders affected by intestinal dilatation syndrome. Article Snippet: Intestinal dilatation syndrome (IDS) is a segmental enteropathy characterized by dilatation of the junction of the ileum and jejunum (Meckel’s diverticulum).. IDS severely affects the poultry industry by causing a chronic and irreversible drop in egg laying, reducing feed conversion efficiency, and increasing the mortality rate.. The clinical and pathological features of IDS in white laying hens were described, and viral molecular and metagenomic research was conducted. Article Title: Identification and functional characterization of the first deep intronic GLA mutation (IVS4+1326C>T) causing renal variant of Fabry disease Article Snippet: Data was analyzed using software Article Title: High viral loads: what drives fatal cases of COVID-19 in vaccinees? – an autopsy study Article Snippet: In addition, the obtained SARS-CoV-2 genome sequences were aligned together and with sequences retrieved from GenBank using MAFFT version 7.388 as implemented in Article Title: Hereditary myotonia in American Bulldog associated with a novel frameshift mutation in the CLCN1 gene. Article Snippet: Hereditary myotonia (HM) is a genetic disorder that occurs due to mutations in the chloride channel and results in delayed relaxation of the skeletal muscles.. HM has been described in 12 dog breeds, and in five of them, molecular studies of this disorder were performed and mutations in the CLCN1 gene were described.. In this study, an affected American Bulldog (AB) with HM clinically characterized by muscle hypertrophy, myotonic discharges, and nondystrophic myotonia with a “warm-up” phenomenon was evaluated, and the candidate canine CLCN1 gene was sequenced. Article Title: Identification and Functional Characterization of the First Deep Intronic GLA Mutation (IVS4+1326C>T) Causing Renal Variant of Fabry Disease Article Snippet: Data was analyzed using software Article Title: Fatal cases after Omicron BA.1 and BA.2 infection: Diffuse alveolar damage occurs only in a minority – results of an autopsy study Article Snippet: In addition, the obtained SARS-CoV-2 genome sequences were aligned together with sequences retrieved from GenBank and Gisaid using MAFFT version 7.38837, as implemented in |