Tag Archives: copy number variation

Data extraction and integration methods are becoming essential to effectively access and take advantage of the huge amounts of heterogeneous genomics and clinical data increasingly available. In this work, we focus on The Cancer Genome Atlas, a comprehensive archive of ...

Genome and transcriptome sequencing applications that rely on variation in sequence depth can be negatively affected if there are systematic biases in coverage. Researchers at Uppsala University, Sweden have investigated patterns of local variation in sequencing coverage by utilising ultra-deep ...