Nature

Challenges in detecting genomic copy number aberrations using next-generation sequencing data and the eXome Hidden Markov Model: a clinical exome-first diagnostic approach

Chromosomal microarray testing is a powerful tool for detecting genomic copy number aberrations. Combinatorial use of fluorescent dyes and oligonucleotide probes has enabled the detection of invisible ...
Nasdaq

Ancestry® Launches AncestryHealth® Powered by Next Generation Sequencing (NGS)

Next generation sequencing offers more comprehensive data on more commonly inherited health conditions LEHI, Utah & SAN FRANCISCO--(BUSINESS WIRE)-- Ancestry®, the global leader in family history and ...
GEN

Special Report: Microarray Not Fade Away

Yes, many are attracted to next-generation sequencing, but loyalty to chip-based phenotyping has its rewards, particularly in screens of large sample sets. The microarray, the legacy technology for ...
Nature

Targeted resequencing for large-scale genomic studies: accelerating NGS throughput using molecular barcodes

Next-generation sequencing (NGS) is a powerful tool for the massively parallel investigation of specific genomic loci. However, sequence capture methodologies are required for time- and cost-effective ...