Cited in
(45)- Exploratory data analysis in large-scale genetic studies
- Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arrays
- PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data
- A note on statistical method for genotype calling of high-throughput single-nucleotide polymorphism arrays
- Removing technical variability in RNA-seq data using conditional quantile normalization
- Exploration, normalization, and genotype calls of high-density oligonucleotide SNP array data
- beadarray
- CGH-Plotter
- AnnotationDbi
- BRLMM
- SNPchip
- VanillaICE
- AnnotationHub
- AnnotationForge
- CellMiner
- BEDOPS
- Cutadapt
- NGS QC Toolkit
- DREME
- ExpTreeDB
- F-Seq
- GMAP
- GeneSigDB
- GEOmetadb
- GSVA
- Genoviz
- GeneHug-GEPIS
- GenomeGraphs
- GSNAP
- OrganismDbi
- Oncomine
- NGS-QC
- pyDNase
- Rtracklayer
- VarSifter
- VariantTools
- VariantAnnotation
- dChipSNP
- PLASQ
- PICNIC
- CARAT
- panp
- GenoSNP
- aroma.affymetrix
- Statistical genomics. Methods and protocols
This page was built for software: oligo
