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2
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Answer:
Answer: Could I consider an ENCODE experiment with two library as two replicates for dif
23 months ago by
i.sudbery
21k
3
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0
replies
3.0k
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Answer:
Answer: Discrepancy between Log2(x) and Log2(x+1) regarding Log2FC
23 months ago by
i.sudbery
21k
6
votes
1
reply
1.4k
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Answer:
Answer: kallisto -s o error
23 months ago by
i.sudbery
21k
0
votes
1
reply
1.4k
views
Comment:
Comment: How to cut some part of the header of reads in FASTQ file?
23 months ago by
i.sudbery
21k
2
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0
replies
2.0k
views
Comment:
Comment: 1 is not found in chromosome sizes file
23 months ago by
i.sudbery
21k
0
votes
1
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1.5k
views
Answer:
Answer: Problem with universe argument in enrichKEGG
23 months ago by
i.sudbery
21k
0
votes
0
replies
1.9k
views
Comment:
Comment: Should I use TPM or TMM to plot gene expression boxplots in RNAseq?
23 months ago by
i.sudbery
21k
0
votes
1
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1.9k
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Comment:
Comment: Should I use TPM or TMM to plot gene expression boxplots in RNAseq?
23 months ago by
i.sudbery
21k
0
votes
1
reply
1.9k
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Comment:
Comment: Should I use TPM or TMM to plot gene expression boxplots in RNAseq?
23 months ago by
i.sudbery
21k
3
votes
1
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1.0k
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Answer:
Answer: Differential expression vs tissue specific expression
23 months ago by
i.sudbery
21k
0
votes
0
replies
10k
views
Comment:
Comment: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
23 months ago by
i.sudbery
21k
0
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0
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10k
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Comment:
Comment: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
23 months ago by
i.sudbery
21k
0
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1
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10k
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Comment:
Comment: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
updated 23 months ago by
Ram
44k • written 23 months ago by
i.sudbery
21k
0
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2
replies
10k
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Comment:
Comment: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
23 months ago by
i.sudbery
21k
0
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1
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10k
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Comment:
Comment: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
23 months ago by
i.sudbery
21k
8
votes
1
reply
10k
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Answer:
Answer: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
23 months ago by
i.sudbery
21k
2
votes
0
replies
1.5k
views
Comment:
Comment: Salmon TPM calculation constant
23 months ago by
i.sudbery
21k
1
vote
0
replies
1.4k
views
Answer:
Answer: Comparing log2-fold changes to find elements with virtually the same log2-fold c
24 months ago by
i.sudbery
21k
1
vote
1
reply
864
views
Answer:
Answer: how to decide the if the IDR result is good or not
24 months ago by
i.sudbery
21k
6
votes
0
replies
1.3k
views
Answer:
Answer: Can FPKM data sets be of any use or are they trash?
24 months ago by
i.sudbery
21k
1
vote
0
replies
902
views
Comment:
Comment: Gene expression normalization sample-wise or feature-wise? which one is the reco
24 months ago by
i.sudbery
21k
0
votes
0
replies
1.0k
views
Comment:
Comment: logFC is negative, need help to get it done
24 months ago by
i.sudbery
21k
0
votes
1
reply
1.9k
views
Comment:
Comment: Modeling RNAseq batch effects using a non-case/control technical replicate
2.0 years ago by
i.sudbery
21k
1
vote
1
reply
1.5k
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Comment:
Comment: How should I deduce the variable from its variance and expectation in the `voom`
2.0 years ago by
i.sudbery
21k
1
vote
0
replies
1.5k
views
Comment:
Comment: How should I deduce the variable from its variance and expectation in the `voom`
2.0 years ago by
i.sudbery
21k
0
votes
1
reply
1.9k
views
Comment:
Comment: Modeling RNAseq batch effects using a non-case/control technical replicate
2.0 years ago by
i.sudbery
21k
0
votes
0
replies
542
views
Comment:
Comment: Gene coverage issue in HG38
2.0 years ago by
i.sudbery
21k
3
votes
1
reply
1.4k
views
Answer:
Answer: Do I need to adjust the pvalue if I am only going to test one gene from omics da
2.0 years ago by
i.sudbery
21k
0
votes
0
replies
1.1k
views
Comment:
Comment: How to summarize the expression of a gene when having expression data from diffe
2.0 years ago by
i.sudbery
21k
3
votes
2
replies
2.9k
views
Comment:
Comment: RNA Editing data from RNA-seq
2.0 years ago by
i.sudbery
21k
1
vote
1
reply
1.3k
views
Comment:
Comment: How to find the most frequent alternative-splicing event from DEXSEQ data?
2.0 years ago by
i.sudbery
21k
0
votes
0
replies
1.3k
views
Comment:
Comment: DESeq2 results function runs very slow on Windows 10
2.0 years ago by
i.sudbery
21k
1
vote
1
reply
2.9k
views
Comment:
Comment: RNA Editing data from RNA-seq
2.0 years ago by
i.sudbery
21k
1
vote
1
reply
1.3k
views
Comment:
Comment: How to find the most frequent alternative-splicing event from DEXSEQ data?
2.0 years ago by
i.sudbery
21k
0
votes
0
replies
1.3k
views
Comment:
Comment: High downstream gene expression
2.0 years ago by
i.sudbery
21k
0
votes
1
reply
1.2k
views
Comment:
Comment: RNASeq differential expression masked by pathways disregulation
2.0 years ago by
i.sudbery
21k
2
votes
1
reply
1.3k
views
Answer:
Answer: High downstream gene expression
2.0 years ago by
i.sudbery
21k
2
votes
0
replies
1.1k
views
Answer:
Answer: mirbase does not have miRNA annotation of my species, what are the alternatives?
2.0 years ago by
i.sudbery
21k
2
votes
0
replies
1.3k
views
Answer:
Answer: isoform compostion (psi) question
2.1 years ago by
i.sudbery
21k
7
votes
0
replies
3.1k
views
Answer:
Answer: Hugely different results between edgeR and DESeq2
2.1 years ago by
i.sudbery
21k
2
votes
0
replies
4.9k
views
Answer:
Answer: STAR aligner can't map too short reads
2.1 years ago by
i.sudbery
21k
0
votes
0
replies
541
views
Power calculations for differential ChIP
statistics
power
Chipseq
2.1 years ago by
i.sudbery
21k
1
vote
0
replies
1.9k
views
Comment:
Comment: UMI-tools deduplication of reads with UMI at the start of the line
2.1 years ago by
i.sudbery
21k
0
votes
1
reply
1.9k
views
Comment:
Comment: UMI-tools deduplication of reads with UMI at the start of the line
2.1 years ago by
i.sudbery
21k
2
votes
1
reply
1.9k
views
Answer:
Answer: UMI-tools deduplication of reads with UMI at the start of the line
2.1 years ago by
i.sudbery
21k
0
votes
1
reply
1.7k
views
Comment:
Comment: Removing umi split off as a separate fastq (RNA-seq)
2.1 years ago by
i.sudbery
21k
1
vote
1
reply
1.7k
views
Answer:
Answer: Removing umi split off as a separate fastq (RNA-seq)
2.1 years ago by
i.sudbery
21k
1
vote
1
reply
2.5k
views
Comment:
Comment: How to make contrasts to find genes DE in one experimental group but NOT in othe
2.1 years ago by
i.sudbery
21k
0
votes
0
replies
5.0k
views
Comment:
Comment: How to extract aligned reads that contain splice junctions from STAR
2.2 years ago by
i.sudbery
21k
2
votes
1
reply
1.7k
views
Comment:
Comment: parallel for 10000 whole exome data
2.2 years ago by
i.sudbery
21k
1,662 results • Page
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