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bioedit software 7.2.1  (Bioedit Company)

 
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    Structured Review

    Bioedit Company bioedit software 7.2.1
    Bioedit Software 7.2.1, supplied by Bioedit Company, 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/software+bioedit+7%2E2%2E1/bioedit+software/pm37562135-47-9-0
    Average 90 stars, based on 1 article reviews
    bioedit software 7.2.1 - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Sequencing:

    Article Title: Whole-exome sequencing reveals a rare missense variant in DTNA in an Iranian pedigree with early-onset atrial fibrillation
    Article Snippet: For the analysis of the sequencing results, the BioEdit software (BioEdit 7.2.1) was applied.

    Article Title: Phylogeography of the Volcano Rabbit (Romerolagus diazi): the Evolutionary History of a Mountain Specialist Molded by the Climatic-Volcanism Interaction in the Central Mexican Highlands
    Article Snippet: Processes such as climate fluctuations together with recent volcanism have driven the diversification and local persistence of biodiversity within theMexican highlands.We reconstruct the phylogeographic pattern and historical demography of the volcano rabbit, Romerolagus diazi, an endemic lagomorph in central Mexico, to elucidate the effect of the climate-volcanism interaction on its evolutionary history.. We sequenced two mtDNA regions for 152 individuals from 45 sample sites located at the volcanic fields Sierra Chichinautzin and Sierra Nevada.. We surveyed the genetic diversity, and reconstructed and dated an intraspecific phylogeny.

    Mutagenesis:

    Article Title: Whole-exome sequencing reveals a rare missense variant in DTNA in an Iranian pedigree with early-onset atrial fibrillation
    Article Snippet: For the analysis of the sequencing results, the BioEdit software (BioEdit 7.2.1) was applied.

    Article Title: Phylogeography of the Volcano Rabbit (Romerolagus diazi): the Evolutionary History of a Mountain Specialist Molded by the Climatic-Volcanism Interaction in the Central Mexican Highlands
    Article Snippet: Processes such as climate fluctuations together with recent volcanism have driven the diversification and local persistence of biodiversity within theMexican highlands.We reconstruct the phylogeographic pattern and historical demography of the volcano rabbit, Romerolagus diazi, an endemic lagomorph in central Mexico, to elucidate the effect of the climate-volcanism interaction on its evolutionary history.. We sequenced two mtDNA regions for 152 individuals from 45 sample sites located at the volcanic fields Sierra Chichinautzin and Sierra Nevada.. We surveyed the genetic diversity, and reconstructed and dated an intraspecific phylogeny.



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    The image illustrates the pedigree, <t>sequencing</t> analysis, and chromatogram of the index family carrying the mutation, c.G681C, in the DTNA gene. A The pedigree of the proband revealed a positive family history of AF and MI. The genotype of the proband and his family members for DTNA transition demonstrated that the proband (III-5), his brother (III-1), and his brother’s children (IV-2 and IV-5) carried the c.G681C mutation of the DTNA gene in a heterozygote form. The other brother (III-3) and his children (IV-3 and IV-4), who were clinically normal, carried the wild type (G) of the nucleotide. B and C The chromatogram of the wild type (homozygote) and the mutant (heterozygote) of the identified transition is depicted respectively in the upper panel and the lower panel. AF: Atrial Fibrillation, MI: Myocardial Infarction
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    The image illustrates the pedigree, <t>sequencing</t> analysis, and chromatogram of the index family carrying the mutation, c.G681C, in the DTNA gene. A The pedigree of the proband revealed a positive family history of AF and MI. The genotype of the proband and his family members for DTNA transition demonstrated that the proband (III-5), his brother (III-1), and his brother’s children (IV-2 and IV-5) carried the c.G681C mutation of the DTNA gene in a heterozygote form. The other brother (III-3) and his children (IV-3 and IV-4), who were clinically normal, carried the wild type (G) of the nucleotide. B and C The chromatogram of the wild type (homozygote) and the mutant (heterozygote) of the identified transition is depicted respectively in the upper panel and the lower panel. AF: Atrial Fibrillation, MI: Myocardial Infarction
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    The image illustrates the pedigree, <t>sequencing</t> analysis, and chromatogram of the index family carrying the mutation, c.G681C, in the DTNA gene. A The pedigree of the proband revealed a positive family history of AF and MI. The genotype of the proband and his family members for DTNA transition demonstrated that the proband (III-5), his brother (III-1), and his brother’s children (IV-2 and IV-5) carried the c.G681C mutation of the DTNA gene in a heterozygote form. The other brother (III-3) and his children (IV-3 and IV-4), who were clinically normal, carried the wild type (G) of the nucleotide. B and C The chromatogram of the wild type (homozygote) and the mutant (heterozygote) of the identified transition is depicted respectively in the upper panel and the lower panel. AF: Atrial Fibrillation, MI: Myocardial Infarction
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    Image Search Results


    The image illustrates the pedigree, sequencing analysis, and chromatogram of the index family carrying the mutation, c.G681C, in the DTNA gene. A The pedigree of the proband revealed a positive family history of AF and MI. The genotype of the proband and his family members for DTNA transition demonstrated that the proband (III-5), his brother (III-1), and his brother’s children (IV-2 and IV-5) carried the c.G681C mutation of the DTNA gene in a heterozygote form. The other brother (III-3) and his children (IV-3 and IV-4), who were clinically normal, carried the wild type (G) of the nucleotide. B and C The chromatogram of the wild type (homozygote) and the mutant (heterozygote) of the identified transition is depicted respectively in the upper panel and the lower panel. AF: Atrial Fibrillation, MI: Myocardial Infarction

    Journal: BMC Cardiovascular Disorders

    Article Title: Whole-exome sequencing reveals a rare missense variant in DTNA in an Iranian pedigree with early-onset atrial fibrillation

    doi: 10.1186/s12872-022-02485-0

    Figure Lengend Snippet: The image illustrates the pedigree, sequencing analysis, and chromatogram of the index family carrying the mutation, c.G681C, in the DTNA gene. A The pedigree of the proband revealed a positive family history of AF and MI. The genotype of the proband and his family members for DTNA transition demonstrated that the proband (III-5), his brother (III-1), and his brother’s children (IV-2 and IV-5) carried the c.G681C mutation of the DTNA gene in a heterozygote form. The other brother (III-3) and his children (IV-3 and IV-4), who were clinically normal, carried the wild type (G) of the nucleotide. B and C The chromatogram of the wild type (homozygote) and the mutant (heterozygote) of the identified transition is depicted respectively in the upper panel and the lower panel. AF: Atrial Fibrillation, MI: Myocardial Infarction

    Article Snippet: For the analysis of the sequencing results, the BioEdit software (BioEdit 7.2.1) was applied.

    Techniques: Sequencing, Mutagenesis