-
```
An anonymous user added a new forum post "most transcripts and many genes
have no reads" in thread "most transcripts and many genes have no reads" at
http://fluxcapacitor.wikidot.com/forum/t-40930…
-
### Background
Until recently, a plant genome sequence could be assumed to consist of sequences corresponding to 1n chromosomes, plus some remaining unplaced scaffolds, and maybe also plastid genomes…
-
As a TL I would to check the report consistency, identify and flag inconsistencies so that we can improve confidence in the report.
**Acceptance Criteria**
- [ ] Identify report rows where the m…
-
Hi
In the documentation it is stated that the input of normalization required is gene expression normalized by gene length (RPKM, FPKM, TPM, RSEM).
Can 3' mRNA sequencing (QuantSeq) be used? Count…
-
Hello--I'm testing dropEst on a dataset generated with the 10X V1 chemistry (https://support.10xgenomics.com/single-cell-gene-expression/sequencing/doc/specifications-sequencing-requirements-for-singl…
-
**Current term details**
```
Term name - 16S recovery software
Term ID - MIXS:0000066
Structured comment name - x16s_recover_software
Definition - Tools used for 16S rRNA gene extraction
```
…
-
I used funannotate software to predict the genes in the assembled metagenomic sequences and obtained the corresponding result files. I want to run steps 4 to 16 in SqueezeMeta, using these result file…
-
Dear @alexdobin
It's a great piece of software and we achieved our assumptions.
Now there is a problem that our manuscript was asked a question by the reviewers. Questions are as follows:
"L48…
-
Hi, thank you for developing such an excellent tool!
I encountered an error while running the `dataprep` function in the xpore software as follows:
```py
KeyError …
-