AIMC Topic: Genetic Variation

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A Sparse Learning Framework for Joint Effect Analysis of Copy Number Variants.

IEEE/ACM transactions on computational biology and bioinformatics Jan 1, 2017
Copy number variants (CNVs), including large deletions and duplications, represent an unbalanced change of DNA segments. Abundant in human genomes, CNVs contribute to a large proportion of human genetic diversity, with impact on many human phenotypes...
Humans Machine Learning Protein Interaction Maps Genomics Databases, Genetic DNA Copy Number Variations Genetic Variation Genome, Human
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Genetics. Predicting the impact of genomic variation.

Nature methods Mar 1, 2016
Humans Computer Simulation Models, Genetic Sequence Analysis, DNA Models, Statistical Unsupervised Machine Learning Genetic Variation Base Sequence Genome, Human Molecular Sequence Data Chromosome Mapping
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[Variability of Cytochrome b Gene and Adjacent Section of Gene tRNA-Thr of Mitochondrial DNA in the Northern Mole Vole Ellobius talpinus (Mammalia, Rodentia)].

Genetika Dec 1, 2015
The Northern mole vole E. talpinus, despite its wide distribution, is characterized by a stable karyotype (2n = NF = 54) and slight morphological polymorphism. We made a preliminary analysis of a mitochondrial DNA fragment to clarify the level of gen...
Animals Male DNA, Mitochondrial Genetic Variation Arvicolinae Cytochromes b RNA, Transfer, Thr
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