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 ...

Venter's aim in doing so was to complete the sequencing of the human genome faster than the government-backed ("public") effort. This competition would later culminate in the simultaneous ...

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 ...

Upper tract urothelial carcinoma (UTUC) is an aggressive disease that is challenging to biopsy and diagnose, frequently yielding nondiagnostic cytology and tissue specimens. Therefore, UTUC is often ...

it's very likely that everyone will move towards whole-genome sequencing because it will be cost-effective. And what that will allow us to do is to detect unusual features in people's cancers that go ...

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 ...