When people think of DNA, they usually think of genes, the parts that code for proteins and drive inherited traits. But there ...

Read depth (RD) signals anomaly-based copy number variation (CNV) detection methods using whole genome sequencing data are affected by the measurement scale and parameters, and the breakpoint of CNVs ...

Market Growth Driven by Declining Sequencing Costs, Rising Prevalence of Genetic Disorders, Expanding Clinical Applications, and Technologica ...

A New Era for Embryo Screening: Juniper Genomics Debuts with World’s First Whole-Genome and Transcriptome Test ...

Pipelines for the analysis of whole-genome bisulfite sequencing data usually consists of four steps: read trimming, read mapping, quantification of methylation levels, and prediction of differentially ...

Genome Sequencing and Assembly. Total DNA of L. crispatus NCK1350 was isolated using an UltraClean Microbial DNA Isolation Kit (MOBIO), and whole-genome sequencing was performed using a MiSeq System ...

Pharmacogenomics Whole genome sequencing looks not only at the DNA of the tumor cells, but also at so-called germline DNA in a child's healthy cells.

Thanks to a collaboration with Simon Elsässer and Jing Lyu from the Karolinska Institute, the team discovered that the G-loop helps untie G4 knots across the entire genome.