The Envisia test uses RNA sequencing and machine learning to diagnose idiopathic pulmonary fibrosis.
The Ivy Glioblastoma Atlas includes newly generated anatomical and transcriptional profiles for dozens of tumors, combined with genomic data from TCGA.
As part of a new partnership, Partek Flow NGS analysis software will help researchers access single-cell RNA sequences without the need for bioinformatics expertise.
While digging into the tumor-suppressive mechanism for an X-linked gene called UTX, researchers found a similar protective role for the Y chromosome gene UTY.
The company recognized $20 million in Q1 revenues and grew its testing volume by 18 percent.
Researchers at the annual Association of Biomolecular Resource Facilities meeting said they are joining single-cell sequencing to other single-cell analyses.
The two studies used Drop-seq RNA profiling to discover essentially all cell types and establish cell lineages in a model organism flatworm.
At the AACR annual meeting, researchers highlighted genomics- and proteomics-informed research aimed at establishing more effective, targeted immunotherapies.
In a training subset of the larger cohort, the company was able to develop classifiers that detected many cancers while minimizing false positives.
The team found that colorectal cancer cells experience substantial increases in somatic mutations compared to normal colorectal cells.
Magdalena Skipper, the incoming editor-in-chief of Nature, speaks with NPR's Weekend Edition Sunday.
Genetic genealogy has led to an arrest in another cold case, dating back to 1987.
In PLOS this week: mutation in second gene widens clinical symptoms of people with ADD3 mutations, comparative genomic analysis of Pseudovibrio, and more.
Wired reports that 23andMe is trying to bolster its outside collaborations.