Skip to content

Problems with processing RNAseq data #7

Description

@maxx19960107

Hi there, Thank you for creating cleancall.
I have some problems when analysis RNA-seq data:
The result file is as follows.
image

How can I get the contamination results of RNA-seq? I only want results that don't need correction.
or is there any problem with my running method?
'''
prod 11:48:21 R290-1: /mnt/GenePlus001/prod/maxx/software/contamination4/dbsnp
$ cat dbsnp_pileup.sh
/mnt/GenePlus001/prod/maxx/software/cleancall/bin/cctools pileup -loci /mnt/GenePlus001/prod/maxx/software/contamination3/dbsnp_138.b37.vcf.gz -index 180022992FR1 -out 180022992FRdbsnp_pileup -ref /products/repos/prod/Akso/BNC_v2/BNC/program/NoahCare/db/alignment/tgp_phase2_flat/hs37d5.fa --run 1 &
prod 11:49:17 R290-1: /mnt/GenePlus001/prod/maxx/software/contamination4/dbsnp
$ cat dbsnp_verify.sh
/mnt/GenePlus001/prod/maxx/software/cleancall/bin/cctools verify -index /mnt/GenePlus001/prod/maxx/software/contamination4/dbsnp/180022992FRdbsnp_pileup.ped -o 180022992FR_verify -vcf /mnt/GenePlus001/prod/maxx/software/contamination3/dbsnp_138.b37.vcf.gz --run 1
'''

Metadata

Metadata

Assignees

No one assigned

    Labels

    No labels
    No labels

    Projects

    No projects

    Milestone

    No milestone

    Relationships

    None yet

    Development

    No branches or pull requests

    Issue actions