Comments (4)
from suppa.
Thank you so much! I'll try it out.
Merry Christmas.
Meng
from suppa.
Hello. You mentioned the PSI is already a normalised value. May I know how you normalised it? Like quantile normalise within samples? Because I tried to quantile normalise PSI within samples and then found the normalised data is really similar to the original data. So I was wondering if I still need to quantile normalise it myself. Thank you so much for your help.
All the best,
Meng
from suppa.
Hi,
no need to perform quantile normalisation of PSI values.
PSI represents a proportion: the proportion of RNA abundance that explain the usage of that exon or event type. It relies on TPM values. These are normalised values as well. However, their distribution may differ between samples. It is worthwhile checking the TPM value distributions and whether it is necessary to perform a TPM normalisation.
from suppa.
Related Issues (20)
- GTF input file HOT 1
- abnormal P-value from the "suppy.py diffSplice" HOT 4
- How to analyze mas-iso-seq data using suppa ? HOT 1
- about nan values HOT 1
- IndexError while using generateEvents HOT 4
- generateEvents option returning empty .ioe files HOT 5
- diffSplice Error HOT 6
- U12 splicing event HOT 4
- Feature Request: Inter-sample PSI Value Comparison for Large Datasets in SUPPA2 HOT 1
- Addressing Batch Effects in Datasets with SUPPA2 HOT 3
- missing lib.tools HOT 1
- Help with generation of PSI results HOT 1
- psiPerEvent - "transcript not found" HOT 6
- Error with diffSplice HOT 4
- Help about rank differential gene HOT 4
- "Differential transcript usage", the cognate gene expression? HOT 1
- diffSplice error,a classic one: 'UnboundLocalError'. I have tried my best. HOT 4
- Issues reading transcript expression files HOT 3
- UnboundLocalError("local variable 'i' referenced before assignment",) HOT 2
- How to Determine Differential Variable Splicing Events (DAS)?
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from suppa.