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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
20 months ago by
i.sudbery
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3
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0
replies
2.6k
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Answer:
Answer: Discrepancy between Log2(x) and Log2(x+1) regarding Log2FC
20 months ago by
i.sudbery
20k
6
votes
1
reply
1.2k
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Answer:
Answer: kallisto -s o error
20 months ago by
i.sudbery
20k
0
votes
1
reply
1.3k
views
Comment:
Comment: How to cut some part of the header of reads in FASTQ file?
21 months ago by
i.sudbery
20k
2
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0
replies
1.8k
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Comment:
Comment: 1 is not found in chromosome sizes file
21 months ago by
i.sudbery
20k
0
votes
1
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1.4k
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Answer:
Answer: Problem with universe argument in enrichKEGG
21 months ago by
i.sudbery
20k
0
votes
0
replies
1.7k
views
Comment:
Comment: Should I use TPM or TMM to plot gene expression boxplots in RNAseq?
21 months ago by
i.sudbery
20k
0
votes
1
reply
1.7k
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Comment:
Comment: Should I use TPM or TMM to plot gene expression boxplots in RNAseq?
21 months ago by
i.sudbery
20k
0
votes
1
reply
1.7k
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Comment:
Comment: Should I use TPM or TMM to plot gene expression boxplots in RNAseq?
21 months ago by
i.sudbery
20k
3
votes
1
reply
910
views
Answer:
Answer: Differential expression vs tissue specific expression
21 months ago by
i.sudbery
20k
0
votes
0
replies
9.4k
views
Comment:
Comment: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
21 months ago by
i.sudbery
20k
0
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0
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9.4k
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Comment:
Comment: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
21 months ago by
i.sudbery
20k
0
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1
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9.4k
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Comment:
Comment: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
updated 21 months ago by
Ram
44k • written 21 months ago by
i.sudbery
20k
0
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2
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9.4k
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Comment:
Comment: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
21 months ago by
i.sudbery
20k
0
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1
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9.4k
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Comment:
Comment: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
21 months ago by
i.sudbery
20k
8
votes
1
reply
9.4k
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Answer:
Answer: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
21 months ago by
i.sudbery
20k
2
votes
0
replies
1.3k
views
Comment:
Comment: Salmon TPM calculation constant
21 months ago by
i.sudbery
20k
1
vote
0
replies
1.3k
views
Answer:
Answer: Comparing log2-fold changes to find elements with virtually the same log2-fold c
21 months ago by
i.sudbery
20k
1
vote
1
reply
792
views
Answer:
Answer: how to decide the if the IDR result is good or not
21 months ago by
i.sudbery
20k
6
votes
0
replies
1.2k
views
Answer:
Answer: Can FPKM data sets be of any use or are they trash?
21 months ago by
i.sudbery
20k
1
vote
0
replies
809
views
Comment:
Comment: Gene expression normalization sample-wise or feature-wise? which one is the reco
21 months ago by
i.sudbery
20k
0
votes
0
replies
916
views
Comment:
Comment: logFC is negative, need help to get it done
21 months ago by
i.sudbery
20k
0
votes
1
reply
1.7k
views
Comment:
Comment: Modeling RNAseq batch effects using a non-case/control technical replicate
21 months ago by
i.sudbery
20k
1
vote
1
reply
1.3k
views
Comment:
Comment: How should I deduce the variable from its variance and expectation in the `voom`
21 months ago by
i.sudbery
20k
1
vote
0
replies
1.3k
views
Comment:
Comment: How should I deduce the variable from its variance and expectation in the `voom`
21 months ago by
i.sudbery
20k
0
votes
1
reply
1.7k
views
Comment:
Comment: Modeling RNAseq batch effects using a non-case/control technical replicate
21 months ago by
i.sudbery
20k
0
votes
0
replies
481
views
Comment:
Comment: Gene coverage issue in HG38
21 months ago by
i.sudbery
20k
3
votes
1
reply
1.2k
views
Answer:
Answer: Do I need to adjust the pvalue if I am only going to test one gene from omics da
21 months ago by
i.sudbery
20k
0
votes
0
replies
1.0k
views
Comment:
Comment: How to summarize the expression of a gene when having expression data from diffe
21 months ago by
i.sudbery
20k
3
votes
2
replies
2.6k
views
Comment:
Comment: RNA Editing data from RNA-seq
22 months ago by
i.sudbery
20k
1
vote
1
reply
1.2k
views
Comment:
Comment: How to find the most frequent alternative-splicing event from DEXSEQ data?
22 months ago by
i.sudbery
20k
0
votes
0
replies
1.2k
views
Comment:
Comment: DESeq2 results function runs very slow on Windows 10
22 months ago by
i.sudbery
20k
1
vote
1
reply
2.6k
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Comment:
Comment: RNA Editing data from RNA-seq
22 months ago by
i.sudbery
20k
1
vote
1
reply
1.2k
views
Comment:
Comment: How to find the most frequent alternative-splicing event from DEXSEQ data?
22 months ago by
i.sudbery
20k
0
votes
0
replies
1.2k
views
Comment:
Comment: High downstream gene expression
22 months ago by
i.sudbery
20k
0
votes
1
reply
1.1k
views
Comment:
Comment: RNASeq differential expression masked by pathways disregulation
22 months ago by
i.sudbery
20k
2
votes
1
reply
1.2k
views
Answer:
Answer: High downstream gene expression
22 months ago by
i.sudbery
20k
2
votes
0
replies
963
views
Answer:
Answer: mirbase does not have miRNA annotation of my species, what are the alternatives?
22 months ago by
i.sudbery
20k
2
votes
0
replies
1.1k
views
Answer:
Answer: isoform compostion (psi) question
22 months ago by
i.sudbery
20k
7
votes
0
replies
2.8k
views
Answer:
Answer: Hugely different results between edgeR and DESeq2
22 months ago by
i.sudbery
20k
2
votes
0
replies
4.2k
views
Answer:
Answer: STAR aligner can't map too short reads
22 months ago by
i.sudbery
20k
0
votes
0
replies
463
views
Power calculations for differential ChIP
statistics
power
Chipseq
22 months ago by
i.sudbery
20k
1
vote
0
replies
1.8k
views
Comment:
Comment: UMI-tools deduplication of reads with UMI at the start of the line
22 months ago by
i.sudbery
20k
0
votes
1
reply
1.8k
views
Comment:
Comment: UMI-tools deduplication of reads with UMI at the start of the line
22 months ago by
i.sudbery
20k
2
votes
1
reply
1.8k
views
Answer:
Answer: UMI-tools deduplication of reads with UMI at the start of the line
22 months ago by
i.sudbery
20k
0
votes
1
reply
1.5k
views
Comment:
Comment: Removing umi split off as a separate fastq (RNA-seq)
22 months ago by
i.sudbery
20k
1
vote
1
reply
1.5k
views
Answer:
Answer: Removing umi split off as a separate fastq (RNA-seq)
22 months ago by
i.sudbery
20k
1
vote
1
reply
2.2k
views
Comment:
Comment: How to make contrasts to find genes DE in one experimental group but NOT in othe
23 months ago by
i.sudbery
20k
0
votes
0
replies
4.6k
views
Comment:
Comment: How to extract aligned reads that contain splice junctions from STAR
23 months ago by
i.sudbery
20k
2
votes
1
reply
1.5k
views
Comment:
Comment: parallel for 10000 whole exome data
23 months ago by
i.sudbery
20k
1,612 results • Page
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