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answers
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replies
9.4k
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Answer:
Answer: How does edgeR do ERCC spike-in normalization?
2.4 years ago by
Bogdan
★ 1.4k
0
votes
1
reply
2.8k
views
Answer:
Answer: converting bedgraph to bigwig by not using ucsc tools
2.7 years ago by
Bogdan
★ 1.4k
2
votes
0
replies
841
views
Answer:
Answer: scATAC-seq
3.1 years ago by
Bogdan
★ 1.4k
2
votes
0
replies
3.6k
views
Answer:
Answer: heatmap of genes pseudotime in monoclle3
3.3 years ago by
Bogdan
★ 1.4k
1
vote
0
replies
3.0k
views
Answer:
A: NMF tools for scRNA analysis
4.4 years ago by
Bogdan
★ 1.4k
1
vote
1
reply
1.3k
views
Answer:
A: Network analysis: where to start?
4.5 years ago by
Bogdan
★ 1.4k
0
votes
2
replies
7.5k
views
Answer:
A: about batch correction in scRNA-seq
5.0 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
5.2k
views
Answer:
A: minimal free energy and RNA folding
5.1 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
2.7k
views
Answer:
A: scRNA-seq : split a SEURAT cluster into 2 sub-clusters
5.3 years ago by
Bogdan
★ 1.4k
6
votes
0
replies
6.9k
views
Answer:
A: Single Cell RNA Seq. Analysis
6.0 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
4.6k
views
Answer:
A: a webserver for the bigwig files
6.2 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
3.8k
views
Answer:
A: gene counts in Seurat after RunCCA() and AlignSubspace()
6.3 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
1.3k
views
Answer:
A: scRNA-seq: a question about the names of the columns in a Seurat object
6.4 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
5.6k
views
Answer:
A: filtering the somatic variants
6.5 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
5.6k
views
Answer:
A: filtering the somatic variants
6.5 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
5.6k
views
Answer:
A: filtering the somatic variants
6.5 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
2.6k
views
Answer:
A: visualization of the translocations on the vertical scale
6.7 years ago by
Bogdan
★ 1.4k
0
votes
1
reply
10k
views
Answer:
A: ChIP seq- input DNA control for normalization
7.4 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
3.8k
views
Answer:
A: calling the CNV in tumor-only samples (WGS and WES)
7.7 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
2.7k
views
Answer:
A: Loss of heterozygosity analysis from SNV files
7.8 years ago by
Bogdan
★ 1.4k
0
votes
2
replies
2.6k
views
Answer:
A: statistical tests to show the specificity of a phenomenon (eg increase in H3K27m
8.2 years ago by
Bogdan
★ 1.4k
0
votes
1
reply
2.6k
views
Answer:
A: statistical tests to show the specificity of a phenomenon (eg increase in H3K27m
8.2 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
5.7k
views
Answer:
A: CNV caller software
8.6 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
3.7k
views
Answer:
A: Hi-C analysis and significant interactions
8.6 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
1.7k
views
Answer:
A: about the genome coordinates for mutations
8.9 years ago by
Bogdan
★ 1.4k
1
vote
0
replies
4.0k
views
Answer:
A: Calculating fold change at enhancers and promoters
9.0 years ago by
Bogdan
★ 1.4k
1
vote
1
reply
4.0k
views
Answer:
A: Calculating fold change at enhancers and promoters
9.0 years ago by
Bogdan
★ 1.4k
2
votes
1
reply
4.0k
views
Answer:
A: Calculating fold change at enhancers and promoters
9.0 years ago by
Bogdan
★ 1.4k
3
votes
0
replies
5.4k
views
Answer:
A: How to analyze RIP-seq data
9.0 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
2.0k
views
Answer:
A: integrate vcf files
9.0 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
2.6k
views
Answer:
A: about the use of varscan, somaticsnipper and samtools
9.2 years ago by
Bogdan
★ 1.4k
0
votes
1
reply
2.6k
views
Answer:
A: about the use of varscan, somaticsnipper and samtools
9.2 years ago by
Bogdan
★ 1.4k
0
votes
0
replies
3.7k
views
Answer:
A: "for loop" and AUTOPLOT function
10.4 years ago by
Bogdan
★ 1.4k
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