Most large structural variants in cancer genomes can be detected without long reads
Abstract Short-read sequencing is the workhorse of cancer genomics yet is thought to miss many structural variants (SVs), particularly large…
Abstract Short-read sequencing is the workhorse of cancer genomics yet is thought to miss many structural variants (SVs), particularly large…
Abstract Phosphofructokinase, platelet (PFKP) is a rate-limiting enzyme of glycolysis that plays a decisive role in various human physio-pathological processes.…
Abstract Intergenic transcription in normal and cancerous tissues is pervasive but incompletely understood. To investigate this, we constructed an atlas…
Abstract Circadian rhythms (CRs) are fundamental biological processes that significantly impact human well-being. Disruption of these rhythms can trigger insufficient…
Abstract Cannabis (Cannabis sativa L.) is one of the earliest cultivated crops, valued for producing a broad spectrum of compounds…
Abstract Background: Whole-genome doubling (WGD) is a common mutation in cancer. Various studies have suggested that WGD is associated with…
Abstract Cancers evolve under the accumulation of thousands of somatic mutations and chromosomal aberrations. While most coding mutations are deleterious,…
Abstract In tumors, somatic mutations of the PTEN suppressor gene are associated with advanced disease, chemotherapy resistance, and poor survival.…
Abstract Precision oncology promises accurate prediction of disease trajectories by utilizing molecular features of tumors. We present a systematic analysis…
Abstract Cancers cause significant mortality and morbidity in adolescents and young adults (AYAs), but their biological underpinnings are incompletely understood.…