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Bioinformatics (Oxford, England)|July 9, 2018
GATK PathSeq: a customizable computational tool for the discovery and identification of microbial sequences in libraries from eukaryotic hostsMark A Walker, Chandra Sekhar Pedamallu, Akinyemi I Ojesina, et al.Nature Neuroscience|December 23, 2020
Overexpression of schizophrenia susceptibility factor human complement C4A promotes excessive synaptic loss and behavioral changes in miceMelis Yilmaz, Esra Yalcin, Jessy Presumey, et al.Genome Research|August 16, 2012
A comprehensive molecular cytogenetic analysis of chromosome rearrangements in gibbonsOronzo Capozzi, Lucia Carbone, Roscoe R Stanyon, et al.Scientific Reports|July 14, 2022
Chromosomal phase improves aneuploidy detection in non-invasive prenatal testing at low fetal DNA fractionsGiulio Genovese, Curtis J Mello, Po-Ru Loh, et al.Genes, Chromosomes & Cancer|November 26, 2014
Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomasGemma Macchia, Karolin H Nord, Monica Zoli, et al.Nature Communications|May 18, 2018
A whole-genome sequence study identifies genetic risk factors for neuromyelitis opticaKarol Estrada, Christopher W Whelan, Fengmei Zhao, et al.Nucleic Acids Research|July 19, 2014
Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancerAlberto L'Abbate, Gemma Macchia, Pietro D'Addabbo, et al.Science (New York, N.Y.)|January 2, 2025
Rare germline structural variants increase risk for pediatric solid tumorsRiaz Gillani, Ryan L Collins, Jett Crowdis, et al.Nature|June 6, 2020
Complement genes contribute sex-biased vulnerability in diverse disordersNolan Kamitaki, Aswin Sekar, Robert E Handsaker, et al.Nature Neuroscience|November 8, 2016
Ultra-rare disruptive and damaging mutations influence educational attainment in the general populationAndrea Ganna, Giulio Genovese, Daniel P Howrigan, et al.Pageof 2