W.H., X.Y., Q.Z., Z.W., C.L., Q.C., M.H., Y. Luo and C.G. performed genome annotation, comparative genomics and genomic variation analysis.
Hänzelmann, S., Castelo, R. & Guinney, J. GSVA: gene set variation analysis for microarray and RNA-seq data.
Copy-number variation analysis was performed with CNVSeq, run with default parameters, and analysis performed on the 'hits' file.
Lam, E. T. et al. Genome mapping on nanochannel arrays for structural variation analysis and sequence assembly.
Marelli, C. et al. Mini-Exome Coupled to Read-Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias.
Hanzelmann S, Castelo R, Guinney J. GSVA: gene set variation analysis for microarray and RNA-seq data.
About: cortex_var is a tool for genome assembly and variation analysis from sequence data.
This review will therefore concentrate on human genetic variation analysis.
Measurements done in different periods of the year permit us to provide a seasonal variation analysis of the C2N.
Mefford, H.C. et al. Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis.
Guo H, Peng Y, Hu Z, et al. Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.
