Please provide your email address to receive an email when new articles are posted on . More than half of individuals appeared unaware they carried predisposition genes. Nearly 40% of carriers would ...
A University of Colorado Cancer study published today in the Journal of the American Medical Informatics Association (JAMIA) describes a new tool that interprets the raw data of whole exome tumor ...
Rare inherited genetic variants significantly increase familial lung cancer risk, offering new targets for early detection.
Disparate Rates of Germline Variants in Cancer Predisposition Genes in African American/Black Compared With Non-Hispanic White Individuals Between 2015 and 2022 The funding sources did not play a role ...
Transformed SCLC from EGFR-mutated LUAD shows a unique mutational profile, complicating treatment approaches and highlighting the need for tailored therapies. Whole exome sequencing revealed ...
A Mayo Clinic study published in Journal of Translational Medicine has evaluated the use of genomic testing broadly for rare diseases. With the increased use of genomic testing such as multi-gene ...
Would you like to sign up for our newsletter and be the first to receive exclusive content, as well as stay informed about our latest solutions and events? Select One Yes No Please select one of the ...
Neoantigen vaccines are at the forefront of cancer research, driving personalized immunotherapy and improving outcomes through targeted T-cell activation.
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback