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1.1k
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Comment:
Comment: Different annotation packages (org.Mm.eg.db, EnsDb.Mmusculus.v79, BiomaRt) retu
3 months ago
ATpoint
★ 4.8k
0
votes
0
replies
282
views
Comment:
Comment: Installation error for Rsamtools.
3 months ago
ATpoint
★ 4.8k
1
vote
0
replies
1.1k
views
Comment:
Comment: Different annotation packages (org.Mm.eg.db, EnsDb.Mmusculus.v79, BiomaRt) retu
3 months ago
ATpoint
★ 4.8k
1
vote
2
replies
1.1k
views
Comment:
Comment: Different annotation packages (org.Mm.eg.db, EnsDb.Mmusculus.v79, BiomaRt) retu
3 months ago
ATpoint
★ 4.8k
0
votes
2
replies
639
views
Answer:
Answer: DESeq2 analysis with transcript counts
3 months ago
ATpoint
★ 4.8k
0
votes
1
reply
1.2k
views
Answer:
Answer: Why did PCA plots look exactly the same after adjusting for batch covariate in D
3 months ago
ATpoint
★ 4.8k
0
votes
1
reply
483
views
Answer:
Answer: DESeq error: counts matrix should be numeric, currently it has mode: character
3 months ago
ATpoint
★ 4.8k
2
votes
0
replies
635
views
Answer:
Answer: Standardization of rlog transformed counts before PCA
4 months ago
ATpoint
★ 4.8k
0
votes
0
replies
1.0k
views
Comment:
Comment: DESeq2: Gene is DEG in one experiment but not in the other depite similar baseMe
4 months ago
ATpoint
★ 4.8k
0
votes
0
replies
1.0k
views
Comment:
Comment: DESeq2: Gene is DEG in one experiment but not in the other depite similar baseMe
4 months ago
ATpoint
★ 4.8k
0
votes
1
reply
1.0k
views
Comment:
Comment: DESeq2: Gene is DEG in one experiment but not in the other depite similar baseMe
4 months ago
ATpoint
★ 4.8k
1
vote
0
replies
2.9k
views
Comment:
Comment: What type of counts data to import for performing Isoform analysis in edgeR
4 months ago
ATpoint
★ 4.8k
2
votes
1
reply
1.0k
views
Answer:
Answer: RSubread output significantly different from bash Subread output
4 months ago
ATpoint
★ 4.8k
1
vote
1
reply
2.9k
views
Comment:
Comment: What type of counts data to import for performing Isoform analysis in edgeR
4 months ago
ATpoint
★ 4.8k
1
vote
1
reply
2.9k
views
Answer:
Answer: What type of counts data to import for performing Isoform analysis in edgeR
4 months ago
ATpoint
★ 4.8k
0
votes
0
replies
366
views
Comment:
Comment: WGCNA with TPM tables
5 months ago
ATpoint
★ 4.8k
0
votes
0
replies
248
views
Comment:
Comment: eRNAs count
5 months ago
ATpoint
★ 4.8k
1
vote
0
replies
364
views
Comment:
Comment: Harmonizing Gene Annotations for Meta-Analysis of GSE68183 and GSE80178
5 months ago
ATpoint
★ 4.8k
0
votes
0
replies
492
views
Answer:
Answer: DESeq2 rerun returns different results
5 months ago
ATpoint
★ 4.8k
1
vote
0
replies
832
views
Answer:
Answer: Handling biological replicates in DESeq2
5 months ago
ATpoint
★ 4.8k
0
votes
1
reply
1.3k
views
Answer:
Answer: Volcano plot has many values around zero
5 months ago
ATpoint
★ 4.8k
2
votes
1
reply
965
views
Comment:
Comment: DESeq Input from Salmon + tximport/tximeta
5 months ago
ATpoint
★ 4.8k
0
votes
0
replies
1.4k
views
Comment:
Comment: Supercells with Basilisk fails for dtype('float64') to dtype('int64') conversion
5 months ago
ATpoint
★ 4.8k
0
votes
0
replies
573
views
Answer:
Answer: Average expression of genes across replicates
5 months ago
ATpoint
★ 4.8k
0
votes
0
replies
651
views
Answer:
Answer: Spike-in normalization method in ATACseq
5 months ago
ATpoint
★ 4.8k
0
votes
0
replies
1.2k
views
Comment:
Comment: New to Deseq2 - DEG questions / MA plot
6 months ago
ATpoint
★ 4.8k
1
vote
1
reply
1.2k
views
Answer:
Answer: Analysis of large RNA-Seq Datasets
6 months ago
ATpoint
★ 4.8k
0
votes
0
replies
378
views
Answer:
Answer: how to extract expression matrix post deseq2
6 months ago
ATpoint
★ 4.8k
1
vote
0
replies
566
views
Answer:
Answer: Automatically generate contrasts from a model matrix / formula
6 months ago
ATpoint
★ 4.8k
1
vote
0
replies
849
views
Comment:
Comment: Mostly increased counts in differentially accessible peaks using DESeq2
6 months ago
ATpoint
★ 4.8k
0
votes
1
reply
324
views
Answer:
Answer: Using Normalized Counts in DESeq2
6 months ago
ATpoint
★ 4.8k
0
votes
1
reply
1.1k
views
Comment:
Comment: What should be the normalization protocol for RNA seq data for WGCNA?
6 months ago
ATpoint
★ 4.8k
1
vote
1
reply
1.1k
views
Answer:
Answer: What should be the normalization protocol for RNA seq data for WGCNA?
6 months ago
ATpoint
★ 4.8k
0
votes
0
replies
734
views
Comment:
Comment: How to control batch effect if Group and batch are same?
6 months ago
ATpoint
★ 4.8k
0
votes
0
replies
849
views
Comment:
Comment: Mostly increased counts in differentially accessible peaks using DESeq2
6 months ago
ATpoint
★ 4.8k
5
votes
1
reply
734
views
Answer:
Answer: How to control batch effect if Group and batch are same?
6 months ago
ATpoint
★ 4.8k
1
vote
0
replies
387
views
Comment:
Comment: Normalization RNA-seq for multiple plates
6 months ago
ATpoint
★ 4.8k
1
vote
0
replies
486
views
Answer:
Answer: DEseq 2 LFC shrinkage with apeglm in single-cell pseudobulk: strange volcano plo
6 months ago
ATpoint
★ 4.8k
0
votes
1
reply
1.2k
views
Answer:
Answer: New to Deseq2 - DEG questions / MA plot
6 months ago
ATpoint
★ 4.8k
1
vote
1
reply
1.1k
views
Comment:
Comment: Size factor normalized counts for between sample comparisons - correct?
7 months ago
ATpoint
★ 4.8k
1
vote
1
reply
1.1k
views
Comment:
Comment: Size factor normalized counts for between sample comparisons - correct?
7 months ago
ATpoint
★ 4.8k
0
votes
1
reply
469
views
Answer:
Answer: Questions in Regards to LFC shrinkage in DSeq2
7 months ago
ATpoint
★ 4.8k
1
vote
0
replies
667
views
Comment:
Comment: Gene filtering in DESeq2
7 months ago
ATpoint
★ 4.8k
1
vote
0
replies
376
views
Answer:
Answer: Deseq2 - differenc in results
7 months ago
ATpoint
★ 4.8k
3
votes
3
replies
757
views
voom does not seem to properly correct for library size
limma
updated 7 months ago by
Gordon Smyth
52k • written 7 months ago by
ATpoint
★ 4.8k
0
votes
0
replies
757
views
Comment:
Comment: voom does not seem to properly correct for library size
7 months ago
ATpoint
★ 4.8k
0
votes
1
reply
841
views
Answer:
Answer: More significant genes after lfcShrink in DEseq2?
8 months ago
ATpoint
★ 4.8k
1
vote
1
reply
1.1k
views
Comment:
Comment: RNASeq normlization for samples with global shift in gene expression
8 months ago
ATpoint
★ 4.8k
2
votes
0
replies
1.1k
views
Answer:
Answer: DESeq2 is it OK to scale transformed data in order to plot heatmaps?
8 months ago
ATpoint
★ 4.8k
2
votes
1
reply
633
views
Answer:
Answer: Why is the inclusion of RUVs not reflected in the EDA plots produced from normal
8 months ago
ATpoint
★ 4.8k
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