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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/result/bioedit software 7.2.1/product/Bioedit Company
Average 90 stars, based on 1 article reviews
bioedit software 7.2.1 - by Bioz Stars, 2026-05
90/100 stars

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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
Software Bioedit 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/result/software bioedit 7.2.1/product/Bioedit Company
Average 90 stars, based on 1 article reviews
software bioedit 7.2.1 - by Bioz Stars, 2026-05
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  Buy from Supplier

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Bioedit Company bioedit v.7.2.1 software
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
Bioedit V.7.2.1 Software, 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/result/bioedit v.7.2.1 software/product/Bioedit Company
Average 90 stars, based on 1 article reviews
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Bioedit Company alignment software bioedit 7.2.1
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
Alignment Software Bioedit 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/result/alignment software bioedit 7.2.1/product/Bioedit Company
Average 90 stars, based on 1 article reviews
alignment software bioedit 7.2.1 - by Bioz Stars, 2026-05
90/100 stars
  Buy from Supplier

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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