AIMC Topic: Chromosomes, Human, Pair 17

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Functional fine-mapping of noncoding risk variants in amyotrophic lateral sclerosis utilizing convolutional neural network.

Scientific reports Jul 30, 2020
Recent large-scale genome-wide association studies have identified common genetic variations that may contribute to the risk of amyotrophic lateral sclerosis (ALS). However, pinpointing the risk variants in noncoding regions and underlying biological...
Humans Neural Networks, Computer Genome-Wide Association Study Genetic Predisposition to Disease Polymorphism, Single Nucleotide Amyotrophic Lateral Sclerosis Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 3
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Structure and Protein Interaction-Based Gene Ontology Annotations Reveal Likely Functions of Uncharacterized Proteins on Human Chromosome 17.

Journal of proteome research Oct 16, 2018
Understanding the function of human proteins is essential to decipher the molecular mechanisms of human diseases and phenotypes. Of the 17 470 human protein coding genes in the neXtProt 2018-01-17 database with unequivocal protein existence evidence ...
Humans Proteome Proteins Databases, Protein Molecular Sequence Annotation Gene Ontology Chromosomes, Human, Pair 17
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