-
Hi Tan,
Sau khi anh git pull ve, bay gio anh co can chay voi param : --unset 9 , nua khogn em?
Thanks !!!
-
I was trying to use [ANNOVAR](http://annovar.openbioinformatics.org/en/latest/) annotated VCF with the Slivar comphet script.
I got the following error:
>[noak@nodecn201 cohort_level]$ ~/resources/…
nroak updated
4 years ago
-
## WGS (Whole Genome Sequencing)
-
Hi,
I am trying to run this tool on WES data, since thie only input file is based on VCF.
I am wondering did you ever applied this method on WES data, and how does it prefoms. Any other suggestions…
-
I have a simple header reading error from markdup that caused my snippy to fail... I've pasted the log file below.
```### echo snippy 4.6.0
### cd /lustre06/project/6000186/congxu/snippy/A.rubrum
…
-
Bonjour,
Il y a une ambiguïté actuellement sur les filtres coding / non coding.
Un variant qui est annoté par Snpeff peut redonner plusieurs transcripts.
Ainsi un variant donné peut avoir un tra…
-
### Description of the bug
i runned sarek to performe a variant calling with a wrong samle file and the samplesheet was not correctly verified
### Command used and terminal output
```console
nextfl…
-
Need to clarify what some of the columns in `variants_long_table.csv` file indicate.
There's some inconsistencies sometimes, for example: `REF_DP` + `ALT_DP` doesn't add up; for indels, often `REF_D…
-
1. SRA to fastq fastqdump -- split-3
2. FastQC
-
First: Thank you. Making data easily available is a great service to the community!
# Issue
MyVariant.info accepts invalid (MyVariant.info-specific) HGVS and does not accept valid HGVS. Since HG…
reece updated
3 years ago