-
Dear Developer, Can I use TOGA to find out the missing and added genes in the query sequence relative to the reference sequence?If so, which result file should I look at?
-
I tried to use sonar-groovy to perform code analysis on our Jenkins pipeline lib written with groovy, but seems it doesn't detect the code duplications. Does it?
-
Can parascopy be used to detect larger duplications e.g. a 1.4 Mb in chromosome 17p11.2 based?
If so, would 30x fq hg38 data like in this example work?
```
@E100046761L1C001R00300000033/1
GGACCT…
-
Hi,
I am going to be using CSUBST in an exploratory manner on a number of genes from a phylogeny and I have both a species tree and gene trees (for each gene) available to me. Can you recommend the…
-
-
Hi,
I have recently aligned the [CHM13](https://github.com/marbl/CHM13) v1.0 assembly from the T2T consortium to the reference genome GRCh38.p13. I subsequently tried to detect SVs from the CHM13 a…
-
Hoping to have the RapiD editor flag the issues below as errors or warnings so that newly created duplicated ways and overlapping ways segments can be eliminated.
#### The following conditions Are…
-
This is a user experience research drawing on 1153 user comments from Google Play reviews of Session for Android between 2020-02 and 2023-11. Employing NLP technology, we have systematically extracted…
-
Seems to be missing on this page. Really is not needed but I think we could add some JS script to auto-generate a card per page. This way every page works on twitter regardless if we add support manua…
-
Hi there,
I would like to apply OFF-PEAK to some targeted EM-seq data (obtained using the Twist Methylome Panel). However, since the tool was designed specifically for exome sequencing data, all ta…