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Briefings in Bioinformatics|July 24, 2001
Genome sequence comparisons: hurdles in the fast lane to functional genomicsT Wiehe, R Guigó, W Miller
Briefings in Bioinformatics|July 24, 2001
Making sense of score statistics for sequence alignmentsM Pagni, C V Jongeneel
Briefings in Bioinformatics|July 29, 2021
GESLM algorithm for detecting causal SNPs in GWAS with multiple phenotypesRuiqi Lyu, Jianle Sun, Dong Xu, et al.
Briefings in Bioinformatics|July 30, 2021
Demystifying emerging bulk RNA-Seq applications: the application and utility of bioinformatic methodologyAmarinder Singh Thind, Isha Monga, Prasoon Kumar Thakur, et al.
Briefings in Bioinformatics|July 30, 2021
Circular RNAs and complex diseases: from experimental results to computational modelsChun-Chun Wang, Chen-Di Han, Qi Zhao, et al.
Briefings in Bioinformatics|July 29, 2021
Addressing data imbalance problems in ligand-binding site prediction using a variational autoencoder and a convolutional neural networkTrinh-Trung-Duong Nguyen, Duc-Khanh Nguyen, Yu-Yen Ou
Briefings in Bioinformatics|October 24, 2018
Copy number aberrations from Affymetrix SNP 6.0 genotyping data-how accurate are commonly used prediction approaches?Adriana Pitea, Ivan Kondofersky, Steffen Sass, et al.
Briefings in Bioinformatics|March 24, 2017
Genome-wide analysis reveals that exon methylation facilitates its selective usage in the human transcriptomeShengli Li, Jiwei Zhang, Shenglin Huang, et al.
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