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GenomicAlignments
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Complete variant toolbox: gmapR/VariantTools/VariantAnnotation - revived
VariantAnnotation
Annotation
GenomicRanges
VariantAnnotation
GenomicAlignments
Annotation
11.1 years ago
Valerie Obenchain
★ 6.8k
0
votes
1
reply
2.5k
views
Worker count specification in functions using bplapply from the BiocParallel pkg
VariantTools
BiocParallel
GenomicAlignments
VariantTools
BiocParallel
GenomicAlignments
updated 11.3 years ago by
Martin Morgan
25k • written 11.3 years ago by
Guest User
★ 13k
0
votes
4
replies
1.9k
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GenomicAlignments and QNAME collision
RNASeq
Cancer
convert
Rsamtools
GenomicAlignments
RNASeq
Cancer
convert
Rsamtools
updated 11.3 years ago by
Stefano Calza
▴ 90 • written 11.3 years ago by
Valerie Obenchain
★ 6.8k
0
votes
7
replies
1.6k
views
GenomicAlignments and QNAME collision
RNASeq
GenomicAlignments
RNASeq
GenomicAlignments
updated 11.4 years ago by
Valerie Obenchain
★ 6.8k • written 11.4 years ago by
Stefano Calza
▴ 90
0
votes
5
replies
2.2k
views
A question about the function readGAlignmentPairs in GenomicRnages package
Alignment
Cancer
convert
GenomicAlignments
Alignment
Cancer
convert
GenomicAlignments
updated 11.5 years ago by
Hervé Pagès
16k • written 11.5 years ago by
Niu, Liang NIH/NIEHS [E]
▴ 50
0
votes
0
replies
993
views
CIGAR-aware coverage
Coverage
GenomicAlignments
Coverage
GenomicAlignments
11.6 years ago
Hervé Pagès
16k
106 results • Page
3 of 3
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Comment: Error Loading Experiment from SimBenchData Package
by
ATpoint
★ 4.9k
Is the Seurat package installed? The error somewhat suggests that it could be related, and at https://www.bioconductor.org/packages/release…
Answer: Help with defining groups
by
Gordon Smyth
53k
Defining sample groups is separate to reading in the DIA-NN data, because the sample conditions and covariates are not necessarily coded in…
Comment: Sharing a collection of datasets in ExperimentHub
by
Peter Hickey
▴ 760
The [**scRNAseq**](https://bioconductor.org/packages/scRNAseq/) package ([source on GitHub](https://github.com/LTLA/scRNAseq)) might serve …
Comment: Using DESeq2 on single cell RNA Seq data of same cell type but different conditi
by
ReinholdGaylord99
• 0
Thank you so much! https://www.nature.com/articles/s41467-021-25960-2/ [geometry dash lite](https://geometrydashlite.online)
Comment: Guidance on limma for pseudobulk scRNA-seq with multi-factor design
by
Gordon Smyth
53k
I'm not sure that I understand. You have a dataset that, even after pseudo-bulking, still has 6000 samples? That is surprising. Retaining …
Votes
Answer: ordinary t from limma [was: How would I normally compare swirl?]
Comment: readDNAStringSet with non DNA characters
Comment: Guidance on limma for pseudobulk scRNA-seq with multi-factor design
Answer: Guidance on limma for pseudobulk scRNA-seq with multi-factor design
Answer: Guidance on limma for pseudobulk scRNA-seq with multi-factor design
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