Package: DNAfusion 1.9.0
DNAfusion: Identification of gene fusions using paired-end sequencing
DNAfusion can identify gene fusions such as EML4-ALK based on paired-end sequencing results. This package was developed using position deduplicated BAM files generated with the AVENIO Oncology Analysis Software. These files are made using the AVENIO ctDNA surveillance kit and Illumina Nextseq 500 sequencing. This is a targeted hybridization NGS approach and includes ALK-specific but not EML4-specific probes.
Authors:
DNAfusion_1.9.0.tar.gz
DNAfusion_1.9.0.zip(r-4.5)DNAfusion_1.9.0.zip(r-4.4)DNAfusion_1.9.0.zip(r-4.3)
DNAfusion_1.9.0.tgz(r-4.4-any)DNAfusion_1.9.0.tgz(r-4.3-any)
DNAfusion_1.9.0.tar.gz(r-4.5-noble)DNAfusion_1.9.0.tar.gz(r-4.4-noble)
DNAfusion_1.9.0.tgz(r-4.4-emscripten)DNAfusion_1.9.0.tgz(r-4.3-emscripten)
DNAfusion.pdf |DNAfusion.html✨
DNAfusion/json (API)
NEWS
# Install 'DNAfusion' in R: |
install.packages('DNAfusion', repos = c('https://bioc.r-universe.dev', 'https://cloud.r-project.org')) |
Bug tracker:https://github.com/ctriermaansson/dnafusion/issues
On BioConductor:DNAfusion-1.9.0(bioc 3.21)DNAfusion-1.8.0(bioc 3.20)
targetedresequencinggeneticsgenefusiondetectionsequencingbioconductor-packagecirculating-tumor-dnagene-fusionliquid-biopsynext-generation-sequencingtargeted-sequencingvariant-calling
Last updated 2 months agofrom:b215285224. Checks:OK: 7. Indexed: yes.
Target | Result | Date |
---|---|---|
Doc / Vignettes | OK | Nov 29 2024 |
R-4.5-win | OK | Nov 29 2024 |
R-4.5-linux | OK | Nov 29 2024 |
R-4.4-win | OK | Nov 29 2024 |
R-4.4-mac | OK | Nov 29 2024 |
R-4.3-win | OK | Nov 29 2024 |
R-4.3-mac | OK | Nov 29 2024 |
Exports:ALK_sequencebreak_positionbreak_position_depthEML4_ALK_analysisEML4_ALK_detectionEML4_sequencefind_variantsintrons_ALK_EML4
Dependencies:abindAnnotationDbiaskpassbamsignalsBHBiobaseBiocBaseUtilsBiocGenericsBiocIOBiocParallelBiostringsbitbit64bitopsblobcachemclicodetoolscpp11crayoncurlDBIDelayedArrayfastmapformatRfutile.loggerfutile.optionsgenericsGenomeInfoDbGenomeInfoDbDataGenomicAlignmentsGenomicFeaturesGenomicRangesgluehttrIRangesjsonliteKEGGRESTlambda.rlatticelifecycleMatrixMatrixGenericsmatrixStatsmemoisemimeopensslpkgconfigplogrpngR6RcppRCurlrestfulrRhtslibrjsonrlangRsamtoolsRSQLitertracklayerS4ArraysS4VectorssnowSparseArraySummarizedExperimentsysTxDb.Hsapiens.UCSC.hg38.knownGeneUCSC.utilsvctrsXMLXVectoryamlzlibbioc
Readme and manuals
Help Manual
Help page | Topics |
---|---|
Identification of ALK breakpoint bases | ALK_sequence |
EML4-ALK breakpoint | break_position |
Read depth at breakpoint | break_position_depth |
Complete EML4-ALK analysis | EML4_ALK_analysis |
Detection of ALK and EML4 breakpoint | EML4_ALK_detection |
Identification of EML4 breakpoint bases | EML4_sequence |
Detect the variants of ALK-EML4 | find_variants |
Detect ALK and EML4 introns of the breakpoint | introns_ALK_EML4 |