By a GenomeWeb staff reporter

NEW YORK (GenomeWeb News) – A genome and exome sequencing study of 91 individuals with chronic lymphocytic leukemia has uncovered CLL-associated mutations in genes and pathways known to contribute to the disease as well as others not suspected previously, including components of the messenger RNA splicing system.

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Jul
14
Sponsored by
Agilent Technologies

This online seminar will outline a recent example of the use of molecular barcoding in combination with next-generation sequencing to detect somatic mosaicism in cancer patients.