Microarray Papers of Note (Sept. — Oct. 2006) Oct 31, 2006 Premium Save for later Click here. File Attachments BAN_Papers_103106.htm BAN_Papers_103106.htm Filed under Microarrays & Multiplexing microarrays Breaking News Cell-Free DNA Sequencing Can Detect Clonal Hematopoiesis in Cancer Patients Study of Medieval Swahili Peoples Finds African, Asian Genetic Ancestry Roddenberry Foundation Grants $1.2M to Elypta, Avalo, Thylacine Biosciences BGI Genomics, Zentya Partner to Launch PCR Fecal Test for Colorectal Cancer in Slovakia SomaLogic CEO Steps Down Amid Board Turnover; Firm's Q4 Revenues Drop 18 Percent The Scan Study Examines Insights Gained by Adjunct Trio RNA Sequencing in Complex Pediatric Disease Cases Researchers in AJHG explore the diagnostic utility of adding parent-child RNA-seq to genome sequencing in dozens of families with complex, undiagnosed genetic disease. Clinical Genomic Lab Survey Looks at Workforce Needs Investigators use a survey approach in Genetics in Medicine Open to assess technologist applications, retention, and workforce gaps at molecular genetics and clinical cytogenetics labs in the US. Study Considers Gene Regulatory Features Available by Sequence-Based Modeling Investigators in Genome Biology set sequence-based models against observational and perturbation assay data, finding distal enhancer models lag behind promoter predictions. Genetic Testing Approach Explores Origins of Blastocyst Aneuploidy Investigators in AJHG distinguish between aneuploidy events related to meiotic missegregation in haploid cells and those involving post-zygotic mitotic errors and mosaicism.