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Comment: How to use htseq-count with several samples ?
2.5 years ago by
VBer
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Comment:
C: Visualization of fold changes of candidate genes as heatmap across multiple inde
3.5 years ago by
VBer
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Comment:
C: Mann-Whitney Test/Wilcoxon but for individual genes between case and control
3.6 years ago by
VBer
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Comment:
C: Mann-Whitney Test/Wilcoxon but for individual genes between case and control
3.6 years ago by
VBer
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761
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Comment:
C: How to make KEGG plots based on the gene list with KO ID
3.6 years ago by
VBer
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Comment:
C: Mann-Whitney Test/Wilcoxon but for individual genes between case and control
3.6 years ago by
VBer
▴ 200
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2.0k
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Comment:
C: Mann-Whitney Test/Wilcoxon but for individual genes between case and control
3.6 years ago by
VBer
▴ 200
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2.0k
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Comment:
C: Mann-Whitney Test/Wilcoxcon but for individual genes between case and control
3.6 years ago by
VBer
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855
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Comment:
C: Methodology: Meta-analysis and integration of published transcriptomics and prot
3.7 years ago by
VBer
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Comment:
C: Hypergeometric test on gene lists
3.7 years ago by
VBer
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C: Justifying Learning Linux For Bioinformatics
3.8 years ago by
VBer
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Comment:
C: Possible reasons mapping percentage abysmally low for miRNA reads?
3.8 years ago by
VBer
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Comment:
C: blastn of reference genome CDS to subject genome gives range of hits, which do n
4.1 years ago by
VBer
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1.2k
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Comment:
C: blastn of reference genome CDS to subject genome gives range of hits, which do n
4.2 years ago by
VBer
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1.2k
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Comment:
C: blastn of reference genome CDS to subject genome gives range of hits, which do n
4.2 years ago by
VBer
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2.0k
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Comment:
C: Possible reasons mapping percentage abysmally low for miRNA reads?
4.2 years ago by
VBer
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2.0k
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Comment:
C: Possible reasons mapping percentage abysmally low for miRNA reads?
4.4 years ago by
VBer
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2.0k
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Comment:
C: Possible reasons mapping percentage abysmally low for miRNA reads?
4.4 years ago by
VBer
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1.9k
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Comment:
C: NOISeq Fold Change calculation seems off?
4.4 years ago by
VBer
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Comment:
C: Remove homozygous reference SNPS present in ALL samples of multi-sample VCF file
4.5 years ago by
VBer
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Comment:
C: getting sequence by combining reference and variants (fasta and vcf files)
4.8 years ago by
VBer
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6.7k
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Comment:
C: Emboss seqret - problem conversion gff+fasta to EMBL
4.8 years ago by
VBer
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3.8k
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Comment:
C: Hard time trying to calculate Allele Frequency and DP from Platypus
4.9 years ago by
VBer
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1.2k
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Comment:
C: Bioinformatics Project this summer
4.9 years ago by
VBer
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3.1k
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Comment:
C: Problem in running NOISeq-sim
4.9 years ago by
VBer
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5.3k
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Comment:
C: bcftools mpileup --max depth : What would be a reasonable setting for this optio
4.9 years ago by
VBer
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6.7k
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Comment:
C: how is the output of bcftools stats calculated?
4.9 years ago by
VBer
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2.2k
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Comment:
C: bcftools stats numbers do not match
4.9 years ago by
VBer
▴ 200
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1
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5.3k
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Comment:
C: bcftools mpileup --max depth : What would be a reasonable setting for this optio
5.1 years ago by
VBer
▴ 200
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6.5k
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Comment:
C: Error using feature counts with DESeq2 : Cannot create DESeqData object
5.1 years ago by
VBer
▴ 200
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1
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6.5k
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Comment:
C: Error using feature counts with DESeq2 : Cannot create DESeqData object
5.1 years ago by
VBer
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1
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6.5k
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Comment:
C: Error using feature counts with DESeq2 : Cannot create DESeqData object
5.1 years ago by
VBer
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3.7k
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Comment:
C: BQSR vs VQSR
5.1 years ago by
VBer
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Comment:
C: What is the importance of checking per base sequence content and per sequence GC
5.1 years ago by
VBer
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1.4k
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Comment:
C: Comparing transcriptomic data of the same species from different developmental s
6.4 years ago by
VBer
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