Showing : genomicalignments • reset
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How to extract coordinates of mismatches from a BAM file lodaded in as a GAlignments?
GenomicAlignments
updated 4 months ago by 16k • written 5 months ago by • 0
4
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2
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1.3k
views
GAlignments Cigar to GRanges
GenomicRanges cigarRangesAlongReferenceSpace GenomicAlignments Cigar
4 months ago pineiroalejandro ▴ 10
1
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2
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1.2k
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Issue with assigning transcript IDs to reads when using summarizeOverlaps(mode = IntersectionNotEmpty)
GenomicAlignments summarizeOverlaps( Smart-seq2 proteinvariantcounting
8 months ago SofieK • 0
4
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5
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1.4k
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Strand information in a GAlignmentsList object derived from strand-specific paired-end RNA-seq data
GenomicAlignments
2.7 years ago Robert Castelo ★ 3.4k
1
vote
0
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839
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Possible to customize the parallel computation used in readGAlignments?
R readGAlignments GenomicAlignments
3.0 years ago chen_ying ▴ 10
3
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4
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1.5k
views
mapToAlignments_issue
GenomicAlignments
updated 3.2 years ago by 16k • written 3.2 years ago by • 0
0
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1
reply
1.7k
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Determining alignment coordinates from BAM file
GenomicAlignments GenomicA
updated 3.4 years ago by • 0 • written 3.4 years ago by • 0
0
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9
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2.4k
views
Subsetting operation on CompressedGRangesList object 'x' produces a result that is too big to be represented as a CompressedList object.
DegNorm GenomicAlignments
3.5 years ago • updated 3.4 years ago Jiping Wang ▴ 90
1
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0
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1.5k
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How could I include the unmapped reads of a BAM file for further analysis?
GenomicAlignments Biostrings Rsamtools
3.6 years ago L ▴ 50
0
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1
reply
3.7k
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Error: BiocParallel errors
Bioconductor metagene GenomicAlignments
updated 3.3 years ago by • 0 • written 3.7 years ago by • 0
0
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0
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866
views
readGAlignmentPairs() hanging while reading reads in specified intervals
genomicalig GenomicAlignments
4.4 years ago Malcolm Perry ▴ 40
0
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1
reply
2.7k
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Error in GenomicAlignments::summarizeOverlaps: attempt to select less than one element in OneIndex
SummarizedExperiment GenomicAlignments
4.6 years ago Matthias Munz ▴ 20
0
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2
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1.3k
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Visualising read alignments in
GenomicAlignments Rsamtools
written 4.6 years ago by • 0
4
votes
4
replies
5.4k
views
Best way to handle tags of bam files
GenomicAlignments bam Rsamtools
written 4.6 years ago by ▴ 20
0
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3
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1.3k
views
first(aln) on GAlignmentPairs object always and only return 2 entries
readGAlignmentPairs GenomicAlignments
4.8 years ago Marco Blanchette ▴ 30
0
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0
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1.3k
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Counting reads in genes with summarizeOverlaps
genomicAlignments summarizeOverlaps
5.3 years ago dequattro.concetta ▴ 10
0
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0
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2.0k
views
summarizeOverlaps - (GenomicAlignments) - gives warnings 'package:stats' may not be available when loading
GenomicAlignments summerizeOverlaps-Method DEXSeq
updated 5.5 years ago by 25k • written 5.5 years ago by ▴ 10
1
vote
2
replies
1.3k
views
Rsamtools/GenomicAlignments segmentation faults
Rsamtools GenomicAlignments
updated 5.5 years ago by 25k • written 5.5 years ago by ▴ 10
4
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4
replies
2.4k
views
Issues loading a BAM file resulted from featurecounts
featurecount rsubread GenomicAlignments
5.6 years ago Konstantinos Yeles ▴ 90
2
votes
2
replies
2.1k
views
"S" bases on mapFromAlignments - counted or not?
genomicalignments
updated 5.7 years ago by 16k • written 5.7 years ago by • 0
0
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8
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2.6k
views
exonsBy does not order exons by ascending rank, is it a bug or outdated documentation?
GenomicFeatures GenomicAlignment GenomicAlignments exonBy coverageByTranscript
updated 5.9 years ago by 16k • written 5.9 years ago by ▴ 90
0
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2
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1.2k
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Should GenomicAlignments::mapToAlignments() terminate when no alignments are found for one read?
GenomicAlignments
updated 5.9 years ago by ★ 6.8k • written 5.9 years ago by ▴ 40
4
votes
6
replies
2.5k
views
How to query a base along an aligned read by genomic position?
GenomicAlignments BAM CIGAR
updated 5.9 years ago by ▴ 740 • written 6.0 years ago by ▴ 40
1
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2
replies
2.0k
views
Coverage function assigns wrong weights for gapped alignments
genomicalignments splicing coverage
updated 6.0 years ago by ★ 11k • written 8.5 years ago by ▴ 10
0
votes
4
replies
1.4k
views
coverageByTranscript coudble counts overlapped region for paired-end data
GenomicAlignments RNA-seq paired-end read coverage
updated 6.2 years ago by 16k • written 6.2 years ago by ▴ 90
1
vote
9
replies
2.1k
views
stackStringsFromBam equivalent for GAlignments with seq
genomicalignments stackStringsFromBam sequenceLayer
6.3 years ago Janet Young ▴ 740
1
vote
8
replies
3.8k
views
How to use Rsamtool or GenomicAlignments to calculate RAN-seq read coverage curves
Rsamtools GenomicAlignments RNA-seq coverage score
updated 6.3 years ago by 16k • written 6.3 years ago by ▴ 90
4
votes
4
replies
1.7k
views
Mimic Counting of HTSeq-count Using countOverlaps
GenomicAlignments countOverlaps
updated 6.4 years ago by 25k • written 6.4 years ago by ★ 1.6k
0
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9
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2.1k
views
summarizeOverlaps bplapply error in DeSeq2 pipeline
summarizeOverlaps R GenomicAlignments
updated 6.4 years ago by 25k • written 6.4 years ago by • 0
3
votes
3
replies
1.5k
views
How to tell a GAlignmentsList singleton is mate1 or mate2
Rsamtools GenomicAlignments GAlignmentsList
updated 6.5 years ago by 68k • written 6.5 years ago by ▴ 100
3
votes
2
replies
1.5k
views
Error in summarizeOverlaps
GenomicAlignments
updated 6.5 years ago by 68k • written 6.5 years ago by • 0
2
votes
1
reply
1.4k
views
Iterating over BAM file by genomic chunk
GenomicAlignments
updated 6.5 years ago by 25k • written 6.5 years ago by 68k
0
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2
replies
1.3k
views
Duplicated reads if 'which' has overlapping reads in ScanBamParam
documentation Rsamtools GenomicAlignments
6.5 years ago Christian Mertes • 0
2
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3
replies
1.7k
views
indexBam(), summarizeOverlaps() error: RNA-seq
genomicAlignments RNA-seq Rsamtools
updated 6.6 years ago by ★ 6.6k • written 6.6 years ago by ▴ 80
1
vote
3
replies
1.6k
views
Efficient counting of nucleotide changes in short-reads
GenomicAlignments Biostrings
updated 6.8 years ago by ★ 11k • written 6.8 years ago by ★ 3.4k
0
votes
1
reply
1.6k
views
Subset bam file in R
rsamtools genomicalignments genomicranges
updated 6.9 years ago by ★ 11k • written 6.9 years ago by • 0
0
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2
replies
1.3k
views
Preparation of summarizedExperiment for dexSeq
dexseq genomicalignments genomicfeatures genomicranges
7.0 years ago A ▴ 60
0
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2
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1.7k
views
Extracting fasta sequences from a RE digested genome .bed file
biostrings genomicalignments rsamtools
updated 7.1 years ago by 16k • written 7.1 years ago by • 0
1
vote
1
reply
1.8k
views
How to parse supplementary (not secondary) alignments
genomicalignments rsamtools
updated 7.1 years ago by 25k • written 7.1 years ago by ▴ 30
0
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1
reply
1.1k
views
Scoring DNA motifs by conservation
conservation sequence genomicalignments
7.2 years ago martin.busch • 0
2
votes
2
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1.5k
views
How to write a preprocess.reads function for summarizeOverlaps that requires different logic for paired and single end reads?
summarizeoverlaps genomicalignments
updated 7.5 years ago by ★ 6.8k • written 7.5 years ago by ★ 7.9k
0
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0
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1.5k
views
large memory footprint with summarizeOverlaps method for BamViews
genomicalignments rsamtools BamViews summarizeoverlaps
updated 7.5 years ago by 25k • written 7.5 years ago by ▴ 10
1
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4
replies
1.9k
views
error displaying bam files
genomicalignments
7.9 years ago kamal.fartiyal84 ▴ 10
5
votes
8
replies
3.2k
views
How to set 'strandMode' with summarizeOverlaps()
GenomicAlignments
7.9 years ago Robert Castelo ★ 3.4k
2
votes
4
replies
2.2k
views
How to build a RNA-seq table of counts for repeatmasker annotations
GenomicFeatures repeatmasker GenomicAlignments
updated 7.9 years ago by ★ 11k • written 7.9 years ago by ★ 3.4k
2
votes
9
replies
2.8k
views
FDR adjustment in Time-Course DATA DESEQ2
deseq2 fdrtool genomicalignments
updated 8.0 years ago by 43k • written 8.0 years ago by ▴ 20
0
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0
replies
1.4k
views
Counting exonic reads with DEXSeq and GenomicAlignments
dexseq genomicalignments exon usage
8.0 years ago igor ▴ 50
5
votes
4
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3.4k
views
how to extract read alignments from reads aligning in mulitple locations
rsamtools genomicalignments genomicfeatures
updated 8.3 years ago by ★ 1.6k • written 8.3 years ago by ★ 3.4k
2
votes
5
replies
2.2k
views
NGS with summarizeOverlaps and SAM files
genomicalignments
updated 8.4 years ago by 68k • written 8.4 years ago by • 0
2
votes
1
reply
1.7k
views
GenomicAlignments/access correct bp positions near indels
genomicranges genomicalignments snp
updated 8.4 years ago by 16k • written 8.4 years ago by ▴ 90
106 results • Page 1 of 3
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Comment: Help with defining groups by Phinney, Brett ▴ 10
I got it working , thank you!!!
Comment: Check removeBatchEffect effectiveness by massimo • 0
I would kindly ask for additional support. When not including the design_timepoint argument in removeBatchEffect and thus keeping the inter…
Comment: Error Loading Experiment from SimBenchData Package by ksankaran • 0
Aha, that was it! The object was class Seurat, but I didn't have it installed. After installing, everything works as expected.
Comment: Streamlining the computing time for MiloDE p-value correction in large dataset? by ATpoint ★ 5.0k
Is a method that is so computationally expensive really beneficial and necessary? You seem to have biological replication, don't you, so ps…
Answer: NA values for DESeq2 p-values and adjusted p-values using large sample sizes by ATpoint ★ 5.0k
Outliers without replacement, independent filtering or all-zero counts for that gene. That's the three options that trigger NAs https://bio…
Votes
Comment: Check removeBatchEffect effectiveness
Gene expression associated with continuous (quantitative) traits (Limma/edgeR/correlation)
Answer: Error Loading Experiment from SimBenchData Package
Comment: incomplete imputation of missing values with LEA impute() function
Answer: Expected memory usage for analyzing large single-cell seq datasets (> 450,000 ce
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