Scientists published Henrietta Lacks’ genome without the consent of her family

The following is an excerpt.

In 1951, Henrietta Lacks, a poor black mother of five living near Baltimore, died from cancer. But cells taken from her tumor lived on. The so-called HeLa cells multiplied prolifically and were sent to labs around the world, where they went on to help develop medical innovations and understanding about vaccines, cancer treatments, cloning and more…

In the story’s latest development, last week scientists published Lacks’ full genome—again, without consent of her family.

View the original article here: Scientists Published Henrietta Lacks’ Genome Without the Consent of Her Family

 

{{ reviewsTotal }}{{ options.labels.singularReviewCountLabel }}
{{ reviewsTotal }}{{ options.labels.pluralReviewCountLabel }}
{{ options.labels.newReviewButton }}
{{ userData.canReview.message }}
skin microbiome x final

Infographic: Could gut bacteria help us diagnose and treat diseases? This is on the horizon thanks to CRISPR gene editing

Humans are never alone. Even in a room devoid of other people, they are always in the company of billions ...
glp menu logo outlined

Newsletter Subscription

* indicates required
Email Lists
glp menu logo outlined

Get news on human & agricultural genetics and biotechnology delivered to your inbox.