A new technique represents an important step forward for single-cell RNA sequencing.
The transcriptome gives a fuller picture of how genes are expressed. RNA sequencing allows for more detailed information on cellular pathways and expression levels in cancer studies.
New 3-D imaging highlights the dynamic and structural interactions of DNA in the nucleus, proving to be a critical missing link in genotype to phenotype.
The first data network for research into Huntington’s disease has been created by an international team, that’s freely available to all scientists.
Synthego has unveiled its CRISPR Pioneers Program to help new researchers conduct successful gene editing experiments.
Breakthrough research published in PLOS ONE demonstrates quantitative, PCR-free detection of microRNA
The human genome consists of Millions of base pairs. A new approach can help to identify genetic triggers for genetic disorders in this flood of data
With over 1,200 cancer whole genome sequences available via Amazon Web Services, cloud solutions generate potential benefits for genomics research
With an introduction to RNA-seq and Q&A moderated by Natalie LaFranzo, PhD, Director of Scientific Projects and Market Development at Cofactor Genomics