Ingrida Domarkienė, a geneticist at Vilnius University in Lithuania, discusses the exciting developments made possible by ...

A SNP (pronounced "snip") is a substitution of one base pair at a given location on the genome. At position 11,294,479 on human chromosome 7, for instance, some people have an A, while others have a G ...

In this study, the genome-wide mean F ST value across all SNP classes was found to be 0.11, interpreted as a moderate level of differentiation. The researchers interpreted F ST values below 0.05 ...

These differences represent tiny tweaks in the genetic code known as single nucleotide polymorphisms, or SNPs. These specific SNPs were then edited into the genome of a gray wolf using CRISPR-Cas9, a ...

Deep learning and ATAC-seq uncover noncoding variants linked to gene regulation and disease in human liver cells.

And that variation reflects evolutionary processes that molded the modern genome. Lander was one of several speakers on these aspects of SNPs at the Fourth International Meeting on Single Nucleotide ...

The Genomics Core now has an Illumina NextSeq500 Next Generation Sequencing (NGS) instrument! This will expand our capacity of services already offered for NGS. Feel free to call or email us to find ...

A new research paper was published in Oncotarget, Volume 16, on April 4, 2025, titled “Association between two single ...

The open source repository of genetic data will delete its banks of data on April 30, its co-founder confirms.

multivariate phenotypic factor and genetic analysis; developmental models; power analysis; extended twin designs; SNP-(co-)heritability; Genomic SEM; Mendelian randomization; responsible conduct of ...