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Ed Winnick

Editor in Chief
Phone
+1-212-651-5619

Edward Winnick is editor in chief of GenomeWeb. E-mail Edward Winnick.

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Articles Authored by Ed Winnick

Jan 12, 2017

JP Morgan Healthcare Conference Day Four: Luminex and Exact Sciences

Jan 12, 2017

JPM Healthcare Day Three: Berry Genomics, PerkinElmer, BGI, GenMark, Guardant Health, Invitae

Jan 11, 2017

JPM Healthcare Day Two: 10x Genomics, Foundation Med, Quidel, Hologic, LabCorp, Nanostring, Bio-Rad

Jan 10, 2017

JP Morgan Healthcare Conference, Day One: Genomic Health, Meridian Bioscience, Qiagen

Jan 14, 2016

JP Morgan Healthcare Day Three: Foundation Med; Cepheid; BD; Invitae; GenMark; Berry Genomics

Jan 13, 2016

JP Morgan Healthcare Day Two: Thermo Fisher; Qiagen; Danaher; Counsyl; Human Longevity; Adaptive Bio

Jan 11, 2016

JP Morgan Healthcare Conference, Day One: 23andMe; Myriad Genetics; Genomic Health; Alere

Jan 22, 2015
Jan 12, 2015

Illumina Launches Four New Systems; Provides Financial, Dx Update at JP Morgan

Jan 14, 2014

Illumina Launches Two New Platforms at JP Morgan Conference; Claims $1,000 Genome

The Scan

UK Team Presents Genetic, Epigenetic Sequencing Method

Using enzymatic DNA preparation steps, researchers in Nature Biotechnology develop a strategy for sequencing DNA, along with 5-methylcytosine and 5-hydroxymethylcytosine, on existing sequencers.

DNA Biobank Developed for French Kidney Donors, Recipients

The KiT-GENIE biobank described in the European Journal of Human Genetics contains DNA samples, genotyping profiles, immune patterns, and clinical features for thousands of kidney donors or transplant recipients in Nantes, France.

Cardiometabolic Disease May Have Distinct Associations With Microbial Metabolites in Blood, Gut

By analyzing gut microbes in combination with related metabolites in feces and blood, researchers in Nature Communications found distinct cardiometabolic disease relationships at each site.

Study Reveals New Details About Genetics of Major Cause of Female Infertility

Researchers in Nature Medicine conducted a whole-exome sequencing study of mote than a thousand patients with premature ovarian insufficiency.