Single nucleotide differences (SNDs) in the dbSNP database may lead to errors in genotyping and haplotyping studies.

Using the focal point approach detailed in the methods, 16,330 SNPs were identified from the re-sequencing of 14 genotypes of the discovery panel, as well as 3,670 validated

To assess whether the MYO5A is the causative gene of the dilute locus in rabbit, DNA markers of this gene were identified and analysed in rabbits of different breeds and the

Specific actions and interventions, manifested in the form of farming skills workshops, farming practice initiatives, mentoring programs, scholarships schemes, improved

In this paper, we address this ability by examining questionnaires and their constructs used in empirical studies reported in the intelligent virtual agent conference proceedings

To elucidate the association between the identified SNP and the outcome of FCoV infection, the frequency of each genotype (Additional file 1) and allele (Additional file 2) was

For each mutation, information is provided at several levels: at the gene level (exon and codon number, wild type and mutant codon, mutational event, mutation name), at the

One person stated, “one should act the way they feel no matter what their gender.” (50-74) Another person said, “they should act like they feel and not pretend to be someone

The effect of SNVs on the functionality of the BRCA1 gene was assessed by means of the PolyPhen2 [10], the Provean [19], the Align GVGD [20], the Strum [9], the Cupsat [21], and