AIMC Topic: INDEL Mutation

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GARFIELD-NGS: Genomic vARiants FIltering by dEep Learning moDels in NGS.

Bioinformatics (Oxford, England) Sep 1, 2018
SUMMARY: Exome sequencing approach is extensively used in research and diagnostic laboratories to discover pathological variants and study genetic architecture of human diseases. However, a significant proportion of identified genetic variants are ac...
Deep Learning Genomics Polymorphism, Single Nucleotide Sequence Analysis, DNA High-Throughput Nucleotide Sequencing INDEL Mutation
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[GENES ALLELE STATUS OF ANGIOTENSINCONVERTING ENZYME (I/D) AND ENDOTHELIAL NITRIC OXIDE SYNTHASE (894 G > T) IN PATIENTS WITH ACUTE CORONARY SYNDROME].

Likars'ka sprava Jan 1, 2015
The association of genes polymorphism of angiotensin-converting enzyme ACE (I/D) and endothelial nitric oxide synthase eNOS (894 G > T) with acute myocardial infarction (MI) among residents of North Bukovina region was evaluated. II/GG and ID/GG hapl...
Humans Prospective Studies Female Risk Factors Aged Aged, 80 and over Adult Male Middle Aged Case-Control Studies Polymorphism, Single Nucleotide Gene Expression Myocardial Infarction Alleles Haplotypes Acute Coronary Syndrome Coronary Vessels Gene Frequency Peptidyl-Dipeptidase A Nitric Oxide Synthase Type III INDEL Mutation
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