机译:拷贝数变异(CNV)对HoxD基因座上远程基因调控的影响
National Research Centre Frontiers in Genetics, School of Life Sciences, Ecole Polytechnique Federate, 1015 Lausanne, Switzerland,Department of Epigenetics, Max-Planck institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany;
National Research Centre Frontiers in Genetics, Department of Genetics and Evolution, University of Geneva, 1211 Geneva 4, Switzerland;
National Research Centre Frontiers in Genetics, School of Life Sciences, Ecole Polytechnique Federate, 1015 Lausanne, Switzerland,National Research Centre Frontiers in Genetics, Department of Genetics and Evolution, University of Geneva, 1211 Geneva 4, Switzerland;
chromatin architecture; enhancer-promoter interaction;
机译:在轨迹处的拷贝数变异(CNV)和单核苷酸多态性(SNP)的共存可能导致将SNP与疾病相关的重要性扭曲
机译:具有多发性硬化症静脉畸形的患者在染色体6p21.32(HLA基因座)上的拷贝数变异(CNV)的定制CGH阵列分析
机译:单个核苷酸变体(SNV),小插入/缺失(诱导),拷贝数变异(CNV)剪切变异(SVS)和基因融合(GF)对NGS的临床验证 平台在Clia设置。
机译:磁性纳米粒子在高通量单核苷酸多态性(SNPs)和拷贝数变异(CNVs)分析中的应用
机译:染色体相互作用及其对基因调控的影响:在果蝇中的男性基因座处进行平移。
机译:开幕文章:拷贝数变异(CNV)对HoxD基因座上远程基因调控的影响
机译:在轨迹处的拷贝数变异(CNV)和单核苷酸多态性(SNP)的共存可能导致将SNP与疾病相关的重要性扭曲