Fabric Genomics, Veritas Genetics Ink Strategic Partnership

Mar 22, 2017

|

NEW YORK (GenomeWeb) – Bioinformatics firm Fabric Genomics — formerly known as Omicia — announced today that it has signed an agreement to incorporate its genome annotation technology into Veritas Genetics' myGenome personal whole-genome sequencing service.

Get the full story

This story is free
for registered users

Registering provides access to this and other free content.

Register now.

Already have an account?
Login Now.

Breaking News

The Scan

Try the Other Version

Researchers find that a personalized medicine approach could help people who experience pain while taking statins, New Scientist reports.

You Do Your Way

US National Science Foundation is continuing its responsible research conduct training policy despite its flaws, ScienceInsider reports.

CRISPR Discussions

A CRISPR-themed meeting explored how the tool could and should be used, Wired reports.

This Week in Science

In Science this week: database of proteins' effects on cancer, targeted error correction sequencing, and more.

Featured White Papers

Hybrid Scaffolding Improves Genome Assembly Accuracy and Contiguity

Bionano Genomics’ Next-Generation Mapping Identifies Large Structural Variants in Cancer and Genetic Disorders

Yield NGS-grade DNA/RNA from 10 or 20 μL of dried blood preserved on a non-invasive collection device

Generating Mouse Models with CRISPR/Cas9

Sep

07

Featured Webinar

Improved Library Prep Workflows for Small RNA NGS in Serum and Plasma

This webinar will address improvements in the library prep workflow for small RNA sequencing in serum and plasma.

Sep

20

Featured Webinar

Latest Advances in Tumor Genomic Profiling for Challenging Samples

This webinar will discuss how next-generation sequencing (NGS) can help clinical research labs and pathologists save time, money, and samples compared to single-analyte oncology research assays.

Sep

21

Featured Webinar

Processing Challenging Tumor Samples via Automated Tissue Dissection and Extraction-Free Library Prep

This webinar will demonstrate a new approach that combines precise FFPE tumor isolation with extraction-free DNA/RNA library preparation to minimize material losses and reduce the amount of tissue input required for NGS analysis.

Sep

26

Featured Webinar

GenomeWeb/ABRF 2017 Webinar Series: CITE-seq: Large-Scale Measurement of Epitopes and Transcriptomes in Single Cells

This webinar will describe a protocol and proof-of-principle experiments for Cellular Indexing of Transcriptome and Epitopes by Sequencing (CITE-seq).

Main menu