| AVANA_Library | Genome-wide annotation for the AVANA sgRNA library | 
| BAGEL_essential | Reference Core fitness essential genes | 
| BAGEL_nonEssential | Reference set of non essential genes | 
| Brunello_Library | Genome-wide annotation for the Brunello sgRNA library | 
| CCLE.gisticCNA | Genome-wide copy number data for 13 human cancer cell lines. | 
| ccr.AnalysisPipeline | CRISPRcleanR analysis pipeline. | 
| ccr.BAM2counts | Raw count file extraction from BAM file list. | 
| ccr.checkCounts | Check consistency between library annotation and count files. | 
| ccr.cleanChrm | Identification and correction of genomic regions of equal log... | 
| ccr.correctCounts | Correction of sgRNA treatment counts for gene independent... | 
| ccr.CreateLibraryIndex | Library index generation based on the sgRNA library to allow... | 
| ccr.ExecuteMageck | Executing MAGeCK from R command line | 
| ccr.FASTQ2counts | FASTQ files alignment and raw count file extraction. | 
| ccr.geneMeanFCs | Gene level log fold changes | 
| ccr.genes2sgRNAs | Targeting sgRNAs | 
| ccr.geneSummary | Gene level depletion summary | 
| ccr.get.CCLEgisticSets | CCLE gistic score gene sets | 
| ccr.getCounts | Convert count inputs in a standard count matrix format. | 
| ccr.get.gdsc1000.AMPgenes | Copy number amplified genes in a given cell line from the... | 
| ccr.getLibrary | Convert library inputs in a standard library annotaion. | 
| ccr.get.nonExpGenes | Non expressed genes in a given cell line | 
| ccr.GWclean | Unsupervised identification and correction of gene... | 
| ccr.impactOnPhenotype | Assessing the impact and potential distortion introduced by... | 
| ccr.logFCs2chromPos | Genomic sorting of sgRNAs' log fold changes. | 
| ccr.multDensPlot | Mutiple shaded density plot | 
| ccr.NormfoldChanges | Normalisation of sgRNA counts and fold change computation | 
| ccr.perf_distributions | CRISPRcleanR correction assessment: inspection of sgRNA log... | 
| ccr.perf_statTests | CRISPRcleanR correction assessment: Statistical tests | 
| ccr.PlainTsvFile | Saving a sgRNA counts' object in plain tsv file | 
| ccr.PrRc_Curve | Classification performances of reference sets of genes (or... | 
| ccr.RecallCurves | CRISPRcleanR correction assessment: Recall curve inspection | 
| ccr.RemoveExtraFiles | Clean intermediate files after pipeline execution. | 
| ccr.ROC_Curve | Classification performances of reference sets of genes (or... | 
| ccr.sgRNAmeanFCs | Extract corrected logFC in vectorial format. | 
| ccr.VisDepAndSig | Depletion profile visualisation with genes signatures... | 
| CL.subset | COSMIC identifiers of 15 immortalised human cancer cell lines | 
| EPLC.272HcorrectedFCs | CRISPRcleanR corrected data for an example cell line | 
| EssGenes.DNA_REPLICATION_cons | Core Fitness essential genes involved in DNA replication | 
| EssGenes.HISTONES | Core Fitness essential histone genes | 
| EssGenes.KEGG_rna_polymerase | Core Fitness essential rna polymerase genes | 
| EssGenes.PROTEASOME_cons | Core Fitness essential proteasome genes | 
| EssGenes.ribosomalProteins | Core Fitness essential genes coding for ribosomal proteins | 
| EssGenes.SPLICEOSOME_cons | Core Fitness essential spliceosome genes | 
| GDSC.CL_annotation | Tissue type and other annotations for 1,001 human cancer cell... | 
| GDSC.geneLevCNA | Genome-wide copy number data for 15 human cancer cell lines. | 
| GeCKO_Library_v2 | Genome-wide annotation for the GeCKO (v2) sgRNA library | 
| HT.29correctedFCs | CRISPRcleanR corrected data for an example cell line | 
| KY_Library_v1.0 | Genome-wide annotation for the Sanger sgRNA Library v1.0 | 
| KY_Library_v1.1 | Genome-wide annotation for the Sanger sgRNA Library v1.1 | 
| MiniLibCas9_Library | Genome-wide annotation for the MiniLibCas9 sgRNA library | 
| RNAseq.fpkms | RNAseq derived genome-wide basal expression profiles for 15... | 
| Whitehead_Library | Genome-wide annotation for the Whitehead sgRNA library | 
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.