The study authors reported no conflicts of interest. Vora reported that her institution received supplies in kind from Illumina for an NIH-funded grant on prenatal whole genome sequencing.

Whole genome sequencing can be an exceptionally valuable tool in cancer diagnostics. The application of this technique can ...

We are conducting a multicenter NIH-funded study to evaluate the clinical and diagnostic utility of trio prenatal whole genome sequencing for pregnancies with complicated fetal structural congenital ...

Microarray analysis identifies more chromosome abnormalities than traditional karyotyping in prenatal testing ... but when combined with certain sequencing strategies, detection of gene ...

China has put Illumina on its ‘unreliable entity list’ after the US imposed sanctions on Beijing Genomics Institute, also a ...

For the current analysis, researchers performed cancer screening of 107 IDENTIFY participants using whole body magnetic ... Turriff et al, Prenatal cfDNA Sequencing and Incidental Detection ...

We are conducting a multicenter NIH-funded study to evaluate the clinical and diagnostic utility of trio prenatal whole genome sequencing for pregnancies with complicated fetal structural congenital ...

The sequencing of the human genome afforded the development of chromosomal ... abnormalities than traditional karyotyping in prenatal testing. Microarrays will also identify findings of unclear ...