Results 41 to 50 of about 499,359 (306)
lncRNASNP2: an updated database of functional SNPs and mutations in human and mouse lncRNAs
Nucleic Acids Res., 2017 Long non-coding RNAs (lncRNAs) are emerging as important regulators in different biological processes through various ways. Because the related data, especially mutations in cancers, increased sharply, we updated the lncRNASNP to version 2 (http ...
Ya-Ru Miao +3 more
semanticscholar +1 more source
SNP-PHAGE – High throughput SNP discovery pipeline [PDF]
BMC Bioinformatics, 2006 AbstractBackgroundSingle nucleotide polymorphisms (SNPs) as defined here are single base sequence changes or short insertion/deletions between or within individuals of a given species. As a result of their abundance and the availability of high throughput analysis technologies SNP markers have begun to replace other traditional markers such as ...
Lakshmi K. Matukumalli +5 more
openaire +3 more sources
RSC AdvancesA sustainable and viable alternative for conventional chemical and physical approaches is the green production of silver nanoparticles (SNPs) using plant extracts.
Sehar Shahzadi +4 more
semanticscholar +1 more source
SNPs in microRNA target sites and their potential role in human disease
Open Biology, 2017 In the post-genomic era, the goal of personalized medicine is to determine the correlation between genotype and phenotype. Developing high-throughput genotyping technologies such as genome-wide association studies (GWAS) and the 1000 Genomes Project ...
Adrianna Moszyńska +3 more
semanticscholar +1 more source
Two single nucleotide polymorphisms in the caprine GnIH gene are associated with litter size
Czech Journal of Animal Science, 2017 Gonadotropin-inhibitory hormone (GnIH) can decrease luteinizing hormone and/or follicle-stimulating hormone levels in rat, mouse, sheep, and cattle by the direct suppression of gonadotropin-releasing hormone (GnRH).
Xiaopeng An +6 more
doaj +1 more source
Scientific Reports, 2017 Single nucleotide polymorphisms (SNPs) are the most abundant DNA sequence variation in the genomes which can be used to associate genotypic variation to the phenotype.
M. Pandey +17 more
semanticscholar +1 more source
Association of a synonymous mutation of the PGAM2 gene and growth traits in rabbits
Czech Journal of Animal Science, 2015 Phosphoglycerate mutase (PGAM2) catalyzes the conversion of 3-phosphoglycerate into 2-phosphoglycerate and releases energy during glycolysis in muscle tissues.
Z.-L. Wu +3 more
doaj +1 more source
Disease-Associated SNPs in Inflammation-Related lncRNAs
Frontiers in Immunology, 2019 Immune-mediated diseases, such as celiac disease, type 1 diabetes or multiple sclerosis, are a clinically heterogeneous group of diseases that share many key genetic triggers.
A. Castellanos-Rubio, S. Ghosh
semanticscholar +1 more source
BioTechniquesGenomic duplications are important sources of structural change and gene innovation. In humans, the most recent and highly identical sequences (>90% homology, >1 kb long) are known as segmental duplications (SDs). Single-nucleotide variants or single-nucleotide polymorphisms within SDs have not been systematically assessed due to limitations around ...
Shapour Jalilzadeh +3 more
openaire +3 more sources
SKM-SNP: SNP markers detection method
Journal of Biomedical Informatics, 2010 SKM-SNP, SNP markers detection program, is proposed to identify a set of relevant SNPs for the association between a disease and multiple marker genotypes. We employ a subspace categorical clustering algorithm to compute a weight for each SNP in the group of patient samples and the group of normal samples, and use the weights to identify the subsets of
Yang Liu 0100 +4 more
openaire +4 more sources