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Comment: I want to correct the erroneous barcode file, and the Python code that I've writ
12 months ago by
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Comment: I want to correct the erroneous barcode file, and the Python code that I've writ
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Comment: Exon vs Transcript in featurecounts for RNA Seq
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Comment: I want to correct the erroneous barcode file, and the Python code that I've writ
12 months ago by
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Comment: I want to correct the erroneous barcode file, and the Python code that I've writ
12 months ago by
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Comment: I want to correct the erroneous barcode file, and the Python code that I've writ
13 months ago by
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Comment: I want to correct the erroneous barcode file, and the Python code that I've writ
13 months ago by
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Comment: I want to correct the erroneous barcode file, and the Python code that I've writ
13 months ago by
i.sudbery
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Comment: I want to correct the erroneous barcode file, and the Python code that I've writ
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Comment: in an RNA-seq experiment, what threshold would you use to define a set of expres
13 months ago by
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Comment: PCA in gene expression
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986
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Comment: PCA in gene expression
13 months ago by
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973
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Comment: How to get human cDNA sequences together with UTR regions?
14 months ago by
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Comment: How to get human cDNA sequences together with UTR regions?
14 months ago by
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Comment: I can not allocate ram memory for WSL2
14 months ago by
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Comment: Tissue-dependent usage of exons
14 months ago by
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954
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Comment: Tissue-dependent usage of exons
14 months ago by
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Comment: How to cut some part of the header of reads in FASTQ file?
14 months ago by
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Comment: 1 is not found in chromosome sizes file
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Comment: Should I use TPM or TMM to plot gene expression boxplots in RNAseq?
14 months ago by
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Comment: Should I use TPM or TMM to plot gene expression boxplots in RNAseq?
14 months ago by
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Comment: Should I use TPM or TMM to plot gene expression boxplots in RNAseq?
14 months ago by
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Comment: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
14 months ago by
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Comment: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
14 months ago by
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Comment:
Comment: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
updated 14 months ago by
Ram
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Comment:
Comment: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
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Comment: How to choose Normalization methods (TPM/RPKM/FPKM) for mRNA expression
14 months ago by
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Comment: Salmon TPM calculation constant
14 months ago by
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653
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Comment: Gene expression normalization sample-wise or feature-wise? which one is the reco
14 months ago by
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664
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Comment: logFC is negative, need help to get it done
14 months ago by
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Comment: Modeling RNAseq batch effects using a non-case/control technical replicate
15 months ago by
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1.1k
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Comment: How should I deduce the variable from its variance and expectation in the `voom`
15 months ago by
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Comment:
Comment: How should I deduce the variable from its variance and expectation in the `voom`
15 months ago by
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Comment: Modeling RNAseq batch effects using a non-case/control technical replicate
15 months ago by
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399
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Comment: Gene coverage issue in HG38
15 months ago by
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762
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Comment: How to summarize the expression of a gene when having expression data from diffe
15 months ago by
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2
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2
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2.2k
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Comment: RNA Editing data from RNA-seq
15 months ago by
i.sudbery
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1.0k
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Comment:
Comment: How to find the most frequent alternative-splicing event from DEXSEQ data?
15 months ago by
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Comment: DESeq2 results function runs very slow on Windows 10
15 months ago by
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2.2k
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Comment:
Comment: RNA Editing data from RNA-seq
15 months ago by
i.sudbery
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Comment:
Comment: How to find the most frequent alternative-splicing event from DEXSEQ data?
15 months ago by
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Comment: High downstream gene expression
15 months ago by
i.sudbery
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966
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Comment: RNASeq differential expression masked by pathways disregulation
15 months ago by
i.sudbery
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1.5k
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Comment:
Comment: UMI-tools deduplication of reads with UMI at the start of the line
16 months ago by
i.sudbery
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1.5k
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Comment:
Comment: UMI-tools deduplication of reads with UMI at the start of the line
16 months ago by
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1.2k
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Comment: Removing umi split off as a separate fastq (RNA-seq)
16 months ago by
i.sudbery
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1.9k
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Comment: How to make contrasts to find genes DE in one experimental group but NOT in othe
16 months ago by
i.sudbery
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4.1k
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Comment:
Comment: How to extract aligned reads that contain splice junctions from STAR
17 months ago by
i.sudbery
19k
2
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1.2k
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Comment:
Comment: parallel for 10000 whole exome data
17 months ago by
i.sudbery
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853
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Comment:
Comment: Evaluating RNASeq counts distribution
18 months ago by
i.sudbery
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