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Nemo
Nemo
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Joined:
5.0 years ago
Last seen:
3.3 years ago
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United States

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Latest posts by user
0 votes
1 reply
1.4K views
Do we have any disease specific SNVs database?
cancer mutation snp snv database
updated by Medhat Medhat • written by Nemo • Nemo
0 votes
2 replies
1.2K views
How should I interpret FB_Plot in microarray analysis?
microarray analysis control quality
updated by Ram Ram • written by Nemo • Nemo
0 votes
6 replies
2.1K views
zero byte files in sratoolkit.3.0.1-ubuntu64
fastq sra-toolkit rna-seq
updated by Ngrin • Ngrin • written by Nemo • Nemo
0 votes
4 replies
2.1K views
Processed RNA seq data publicly available
rna-seq
updated by Ram Ram • written by Nemo • Nemo
0 votes
0 replies
0 views
Comment: Comment: Combining multiple datasets increases the fgsea p-value
written by Nemo • Nemo
0 votes
3 replies
1.7K views
Combining multiple datasets increases the fgsea p-value
enrichment fgsea dataset
updated by mark.ziemann mark.ziemann • written by Nemo • Nemo
0 votes
1 reply
0 views
Comment: Comment: What is the default/best practice to map prob IDs to gene IDs
written by Nemo • Nemo
0 votes
3 replies
1.3K views
What is the default/best practice to map prob IDs to gene IDs
gsea map gene prob
updated by barslmn • barslmn • written by Nemo • Nemo
0 votes
2 replies
1.2K views
Question regarding pathways and cell types
signaling types cell pathway
updated by LauferVA LauferVA • written by Nemo • Nemo
0 votes
0 replies
0 views
Comment: Comment: predict gain/ loss of function from mutation
written by Nemo • Nemo
0 votes
1 reply
0 views
Comment: Comment: predict gain/ loss of function from mutation
written by Nemo • Nemo
0 votes
3 replies
1.3K views
predict gain/ loss of function from mutation
protein mutation loss gain
written by Nemo • Nemo
0 votes
1 reply
1.1K views
Get variant type from genotype data
type missense mutation nonsense variant
updated by Sam Sam • written by Nemo • Nemo
0 votes
1 reply
0 views
Comment: Comment: Htseq-count output file having a high number of __not_aligned
written by Nemo • Nemo
0 votes
3 replies
1.7K views
Htseq-count output file having a high number of __not_aligned
read htseq-count human counts genome alignment
updated by Shred Shred • written by Nemo • Nemo
0 votes
0 replies
622 views
The region for RNase P gene in human genome
gene genome read count
written by Nemo • Nemo
0 votes
1 reply
851 views
How parse collectReadCounts output in r?
collectreadcounts r gatk rstudio
updated by Istvan Albert Istvan Albert • written by Nemo • Nemo
0 votes
0 replies
0 views
Comment: Comment: Get distribution of enrichment scores across all permutations in fgsea
written by Nemo • Nemo
0 votes
1 reply
962 views
aligning RNA seq data against human genome
variant calling rna-seq alignment
updated by GenoMax GenoMax • written by Nemo • Nemo
0 votes
1 reply
0 views
Comment: Comment: Get distribution of enrichment scores across all permutations in fgsea
written by Nemo • Nemo
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