Results 41 to 50 of about 384,456 (306)
A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia [PDF]
We report a genome-wide assessment of single nucleotide polymorphisms (SNPs) and copy number variants (CNVs) in schizophrenia. We investigated SNPs using 871 patients and 863 controls, following up the top hits in four independent cohorts comprising 1 ...
Rujescu, D. +218 more
core +1 more source
El complejo mayor de Histocompatibilidad (MHC del inglés: Major histocompatibility complex) en pollos (Gallus gallus) se encuentra localizado en un micro cromosoma, el 16 del genoma aviar. Así como ocurre en otras especies tiene una fuerte asociación con
Gabriela Marisa Iglesias
doaj +1 more source
Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans [PDF]
The identification of quantitative trait loci (QTLs) of small effect size that underlie complex traits poses a particular challenge for geneticists due to the large sample sizes and large numbers of genetic markers required for genomewide association ...
Plomin, R. +14 more
core +1 more source
SNP-PHAGE – High throughput SNP discovery pipeline [PDF]
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
Two single nucleotide polymorphisms in the caprine GnIH gene are associated with litter size
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
SKM-SNP: SNP markers detection method
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
Association of a synonymous mutation of the PGAM2 gene and growth traits in rabbits
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
Genomic 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
ALL-samples-Q30-snps-recal-beagle-polymorphic.vcf [PDF]
Variant call format (VCF) file for 16 Gopherus polyphemus samples for the publication: Elbers, J.P., R.W. Clostio, and S.S. Taylor (2016) Population genetic inferences using immune gene SNPs mirror patterns inferred by microsatellites.
Sabrina S. Taylor (164358) +5 more
core +1 more source
Association of bovine PPARGC1A and OPN genes with milk production and composition in Holstein cattle
Several studies have reported quantitative trait loci on chromosome 6 affecting milk production and composition traits in dairy cattle. Osteopontin (OPN) and peroxisome proliferator activated receptor-γ coactivator-1α (PPARGC1A) genes have been located ...
M. Pasandideh +3 more
doaj +1 more source

