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BMC Medical Genomics|February 13, 2021
Integrated analysis of differentially expressed genes and construction of a competing endogenous RNA network in human Huntington neural progenitor cellsXiaoping Tan, Yang Liu, Taiming Zhang, et al.BMC Medical Genomics|February 19, 2021
Identification of biomarkers and pathogenesis in severe asthma by coexpression network analysisZeyi Zhang, Jingjing Wang, Ou ChenBMC Medical Genomics|February 24, 2021
Identification of a novel TP63 mutation causing nonsyndromic cleft lip with or without cleft palateTianhui Xu, Mengmeng Du, Xinhua Bu, et al.BMC Medical Genomics|February 24, 2021
Identification of major depressive disorder disease-related genes and functional pathways based on system dynamic changes of network connectivityRuijie Geng, Xiao HuangBMC Medical Genomics|February 24, 2021
Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in gliomaEge Ülgen, Özge Can, Kaya Bilguvar, et al.BMC Medical Genomics|February 26, 2021
Integrated CNV-seq, karyotyping and SNP-array analyses for effective prenatal diagnosis of chromosomal mosaicismNa Ma, Hui Xi, Jing Chen, et al.BMC Medical Genomics|February 6, 2021
Prognostic value of eight immune gene signatures in pancreatic cancer patientsWenting Wang, Zhijian Xu, Ning Wang, et al.BMC Medical Genomics|March 2, 2021
Determining mutational burden and signature using RNA-seq from tumor-only samplesErik Jessen, Yuanhang Liu, Jaime Davila, et al.BMC Medical Genomics|March 3, 2021
A de novo frameshift variant of ANKRD11 (c.1366_1367dup) in a Chinese patient with KBG syndromeJing Chen, Zhongmin Xia, Yulin Zhou, et al.BMC Medical Genomics|February 13, 2021
MIPP-Seq: ultra-sensitive rapid detection and validation of low-frequency mosaic mutationsRyan N Doan, Michael B Miller, Sonia N Kim, et al.Pageof 276