User: Arindam Ghosh
Arindam Ghosh • 350
- Reputation:
- 350
- Status:
- Trusted
- Location:
- Finland
- Website:
- https://ag1805x.github...
- Twitter:
- ag1805x
- Scholar ID:
- Google Scholar Page
- Last seen:
- 2 weeks, 4 days ago
- Joined:
- 5 years, 4 months ago
- Email:
- a******@outlook.in
I am a Early Stage Researcher at the University of Eastern Finland, Kuopio. I hold an undergraduate (B.Sc.) degree in Biotechnology from West Bengal University of Technology, India and a postgraduate (M.Sc.) degree in Bioinformatics from Alagappa University, India. My current research interests include stem cell bioinformatics, RNA-seq data analysis and network biology.
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... I have aligned raw RNA-seq reads to the Ensembl reference genome. I intend to quantify the expression using FeatureCounts of only say lincRNAs. What would be a better approach, use the full GTF file containing all types of RNAs or create a GTF containing only lincRNA and then use as input for Featur ...
written 7 months ago by
Arindam Ghosh • 350
• updated
7 months ago by
Shalu Jhanwar • 490
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... Which tool did you use to generate expression values? I usually use FeatureCounts and I have not experienced float expression value yet. Also please check if the expression values are raw counts or has been pre-normalised. Float expression values are possible after normalisation. DESeq2 requires non ...
written 7 months ago by
Arindam Ghosh • 350
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... This seems something similar that I am planning to execute. Could you share some insights from your analysis that I should keep in mind while performing the analysis? ...
written 7 months ago by
Arindam Ghosh • 350
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... A minimal quality trimming can be done to remove low quality bases (phred < 20) and adapters if present.
For RNA-seq data I usually go by a rule to keep the minimum length to 80% of read length. I haven't come across any standard regarding the min len to set but longer reads are good for alignm ...
written 7 months ago by
Arindam Ghosh • 350
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Comment:
C: GO and KEGG from DESeq2 counts
... Just curious to know why edgeR works with GOana whille DESeq2 doesn't. Both gives a list of genes and I have performed GO analysis based on this list on web via DAVID and Panther. What's the difference with R packages? ...
written 7 months ago by
Arindam Ghosh • 350
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... Since the input file is `txt` while it is looking for `csv` file you have to specify the delimiter argument. Else re-save the file with extension `.csv`. that should work. ...
written 7 months ago by
Arindam Ghosh • 350
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349
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2
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... Can you put up the FastQC GC content plot? ...
written 7 months ago by
Arindam Ghosh • 350
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... Have you checked the `--rna-strandness` option? ...
written 7 months ago by
Arindam Ghosh • 350
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4
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Comment:
C: GTF/GFF for non-coding RNA
... Would be valid to use the gene_biotype specific gtf file for quantification after reads have been aligned to the reference genome? ...
written 7 months ago by
Arindam Ghosh • 350
0
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... I am working with human miRNA-seq data. For alignment, I tried using two tools - BowTie2 and HiSat2 to align the clean reads to the reference genome GRCh38. Interestingly, I observed that HiSat2 provides more unique alignment that Bowtie2. The overall alignment rate was 10-20% higher in case of HiSa ...
written 7 months ago by
Arindam Ghosh • 350
• updated
3 months ago by
Biostar ♦♦ 20
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