Package: TAPseq 1.19.0
TAPseq: Targeted scRNA-seq primer design for TAP-seq
Design primers for targeted single-cell RNA-seq used by TAP-seq. Create sequence templates for target gene panels and design gene-specific primers using Primer3. Potential off-targets can be estimated with BLAST. Requires working installations of Primer3 and BLASTn.
Authors:
TAPseq_1.19.0.tar.gz
TAPseq_1.19.0.zip(r-4.5)TAPseq_1.19.0.zip(r-4.4)TAPseq_1.19.0.zip(r-4.3)
TAPseq_1.19.0.tgz(r-4.4-any)TAPseq_1.19.0.tgz(r-4.3-any)
TAPseq_1.19.0.tar.gz(r-4.5-noble)TAPseq_1.19.0.tar.gz(r-4.4-noble)
TAPseq_1.19.0.tgz(r-4.4-emscripten)TAPseq_1.19.0.tgz(r-4.3-emscripten)
TAPseq.pdf |TAPseq.html✨
TAPseq/json (API)
NEWS
# Install 'TAPseq' in R: |
install.packages('TAPseq', repos = c('https://bioc.r-universe.dev', 'https://cloud.r-project.org')) |
Bug tracker:https://github.com/argschwind/tapseq/issues
- bone_marrow_genex - Mouse bone marrow 10x data
- chr11_genes - Chromosome 11 genes
- chr11_polyA_sites - Chromosome 11 polyA sites
- chr11_primers - Chromosome 11 primers
- chr11_truncated_txs - Chromosome 11 truncated transcripts
- chr11_truncated_txs_seq - Chromosome 11 truncated transcript sequences
On BioConductor:TAPseq-1.19.0(bioc 3.21)TAPseq-1.18.0(bioc 3.20)
singlecellsequencingtechnologycrisprpooledscreens
Last updated 2 months agofrom:e6e4d9cd86. Checks:OK: 1 WARNING: 6. Indexed: yes.
Target | Result | Date |
---|---|---|
Doc / Vignettes | OK | Dec 18 2024 |
R-4.5-win | WARNING | Dec 18 2024 |
R-4.5-linux | WARNING | Dec 18 2024 |
R-4.4-win | WARNING | Dec 18 2024 |
R-4.4-mac | WARNING | Dec 18 2024 |
R-4.3-win | WARNING | Dec 18 2024 |
R-4.3-mac | WARNING | Dec 18 2024 |
Exports:beads_oligobeads_oligo<-blastPrimerscheckPrimerscreateBLASTDbcreateIORecordcreatePrimerTrackdesignPrimersexportPrimerTrackgetTxsSeqinferPolyASitesmin_primer_regionmin_primer_region<-pcr_productspickPrimersplotTargetGenesprimer_max_tmprimer_max_tm<-primer_min_tmprimer_min_tm<-primer_num_returnprimer_num_return<-primer_opt_tmprimer_opt_tm<-primerDataFrameproduct_size_rangeproduct_size_range<-reverse_primerreverse_primer<-selectTargetGenessequence_idsequence_id<-sequence_templatetapseq_primersTAPseqInputtarget_annottarget_annot<-target_sequencetarget_sequence<-truncateTxsPolyATsIOTsIOList
Dependencies:abindAnnotationDbiaskpassBHBiobaseBiocGenericsBiocIOBiocParallelBiostringsbitbit64bitopsblobBSgenomecachemclicodetoolscpp11crayoncurlDBIDelayedArraydplyrfansifastmapformatRfutile.loggerfutile.optionsgenericsGenomeInfoDbGenomeInfoDbDataGenomicAlignmentsGenomicFeaturesGenomicRangesgluehttrIRangesjsonliteKEGGRESTlambda.rlatticelifecyclemagrittrMatrixMatrixGenericsmatrixStatsmemoisemimeopensslpillarpkgconfigplogrpngpurrrR6RCurlrestfulrRhtslibrjsonrlangRsamtoolsRSQLitertracklayerS4ArraysS4VectorssnowSparseArraystringistringrSummarizedExperimentsystibbletidyrtidyselectUCSC.utilsutf8vctrswithrXMLXVectoryamlzlibbioc
Readme and manuals
Help Manual
Help page | Topics |
---|---|
Accessors for TsIO objects | accessors beads_oligo beads_oligo<- min_primer_region min_primer_region<- pcr_products primer_max_tm primer_max_tm<- primer_min_tm primer_min_tm<- primer_num_return primer_num_return<- primer_opt_tm primer_opt_tm<- product_size_range product_size_range<- reverse_primer reverse_primer<- sequence_id sequence_id<- sequence_template tapseq_primers target_annot target_annot<- target_sequence target_sequence<- |
Mouse bone marrow 10x data | bone_marrow_genex |
Check primers for complementarity | checkPrimers checkPrimers,TsIO-method checkPrimers,TsIOList-method |
Chromosome 11 genes | chr11_genes |
Chromosome 11 polyA sites | chr11_polyA_sites |
Chromosome 11 primers | chr11_primers |
Chromosome 11 truncated transcripts | chr11_truncated_txs |
Chromosome 11 truncated transcript sequences | chr11_truncated_txs_seq |
Create boulder IO record | createIORecord createIORecord,TsIO-method createIORecord,TsIOList-method |
Design primers | designPrimers designPrimers,TsIO-method designPrimers,TsIOList-method |
Estimate primer off-targets using BLAST | blastPrimers blastPrimers,TsIO-method blastPrimers,TsIOList-method createBLASTDb estimateOffTargets |
Export TAP-seq primers | createPrimerTrack createPrimerTrack,TsIO-method createPrimerTrack,TsIOList-method exportPrimers exportPrimerTrack primerDataFrame primerDataFrame,TsIO-method primerDataFrame,TsIOList-method |
Get transcript sequences | getTxsSeq getTxsSeq,GRanges-method getTxsSeq,GRangesList-method |
Infer polyA sites from droplet sequencing data | inferPolyASites |
Pick best TAP-seq primers | pickPrimers pickPrimers,TsIO-method pickPrimers,TsIOList-method |
Select target genes | plotTargetGenes selectTargetGenes |
TAPseq: R-package to design primers for TAP-seq | TAPseq |
Create TAPseq input from target sequences | TAPseqInput |
Truncate transcripts at polyA sites | truncateTxsPolyA truncateTxsPolyA,GRanges-method truncateTxsPolyA,GRangesList-method |
TsIO class | beads_oligo,TsIO-method beads_oligo<-,TsIO-method min_primer_region,TsIO-method min_primer_region<-,TsIO-method pcr_products,TsIO-method primer_max_tm,TsIO-method primer_max_tm<-,TsIO-method primer_min_tm,TsIO-method primer_min_tm<-,TsIO-method primer_num_return,TsIO-method primer_num_return<-,TsIO-method primer_opt_tm,TsIO-method primer_opt_tm<-,TsIO-method product_size_range,TsIO-method product_size_range<-,TsIO-method reverse_primer,TsIO-method reverse_primer<-,TsIO-method sequence_id,TsIO-method sequence_id<-,TsIO-method sequence_template,TsIO-method tapseq_primers,TsIO-method target_annot,TsIO-method target_annot<-,TsIO-method target_sequence,TsIO-method target_sequence<-,TsIO-method TsIO TsIO-class |
TsIOList class | pcr_products,TsIOList-method sequence_id,TsIOList-method sequence_template,TsIOList-method tapseq_primers,TsIOList-method target_annot,TsIOList-method target_sequence,TsIOList-method TsIOList TsIOList-class |