-
Notifications
You must be signed in to change notification settings - Fork 8
New issue
Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.
By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.
Already on GitHub? Sign in to your account
Issue --end flag resquested in whole alignment Nanocaller #5
Comments
For NanoCaller, you are required to specify a contig name. The -end flag is optional in the sense that if a user does not provide a value for -end flag, then we use the reference genome FASTA file(.fai index file to be precise) to infer the end coordinates for the specified contig. Are you providing an indexed reference genome FASTA file, and are you specifying a contig? |
I'm not specifying a contig name because I want to extract the SNPs and
indels in all the contigs, when you mean contig name is a general name for
all the contigs?
Thanks
El mié., 9 sept. 2020 a las 15:07, umahsn (<[email protected]>)
escribió:
… For NanoCaller, you are required to specify a contig name. The -end flag
is optional in the sense that if a user does not provide a value for -end
flag, then we use the reference genome FASTA file(.fai index file to be
precise) to infer the end coordinates for the specified contig. Are you
providing an indexed reference genome FASTA file, and are you specifying a
contig?
—
You are receiving this because you authored the thread.
Reply to this email directly, view it on GitHub
<#5 (comment)>, or
unsubscribe
<https://github.com/notifications/unsubscribe-auth/AHFDTT6XI3CRYU6BHPOKFATSE7N63ANCNFSM4RC6743Q>
.
--
*Adriana María Gallego Rúa*
*Investigadora **Laboratorio de Biotecnología*
*Universidad de Antioquia*
*ColombiaMedellín-2020*
|
This is the specific error is showing
in_dict={'chrom':args.chrom, 'start':start, 'end':end,
'sam_path':args.bam, 'fasta_path':args.ref, \
NameError: name 'end' is not defined
When I run next script
NanoCaller.py -bam file.sorted.bam -mode both -seq pacbio -model
NanoCaller3 -vcf nanocaller -chrom CHROM -ref contigs_assembly.fasta
-prefix my_test -cpu 32
And the reference fasta file as well the .fai file are both in the same
directory
Thanks
El mié., 9 sept. 2020 a las 15:20, adriana gallego (<
[email protected]>) escribió:
… I'm not specifying a contig name because I want to extract the SNPs and
indels in all the contigs, when you mean contig name is a general name for
all the contigs?
Thanks
El mié., 9 sept. 2020 a las 15:07, umahsn ***@***.***>)
escribió:
> For NanoCaller, you are required to specify a contig name. The -end flag
> is optional in the sense that if a user does not provide a value for -end
> flag, then we use the reference genome FASTA file(.fai index file to be
> precise) to infer the end coordinates for the specified contig. Are you
> providing an indexed reference genome FASTA file, and are you specifying a
> contig?
>
> —
> You are receiving this because you authored the thread.
> Reply to this email directly, view it on GitHub
> <#5 (comment)>,
> or unsubscribe
> <https://github.com/notifications/unsubscribe-auth/AHFDTT6XI3CRYU6BHPOKFATSE7N63ANCNFSM4RC6743Q>
> .
>
--
*Adriana María Gallego Rúa*
*Investigadora **Laboratorio de Biotecnología*
*Universidad de Antioquia*
*ColombiaMedellín-2020*
--
*Adriana María Gallego Rúa*
*Investigadora **Laboratorio de Biotecnología*
*Universidad de Antioquia*
*ColombiaMedellín-2020*
|
The problem is that the specified contig or chromosome is not found in the reference .fai file. Can you confirm whether that is the case or not? |
We have addressed several of your concerns in an updated version of NanoCaller. Please refer to issue #6. |
Thanks!
El lun., 21 sept. 2020 a las 14:08, umahsn (<[email protected]>)
escribió:
… We have addressed several of your concerns in an updated version of
NanoCaller. Please refer to issue #6
<#6>.
—
You are receiving this because you authored the thread.
Reply to this email directly, view it on GitHub
<#5 (comment)>, or
unsubscribe
<https://github.com/notifications/unsubscribe-auth/AHFDTTZ35RMVMW6VRAK7XFDSG6QB5ANCNFSM4RC6743Q>
.
--
*Adriana María Gallego Rúa*
*Investigadora **Laboratorio de Biotecnología*
*Universidad de Antioquia*
*ColombiaMedellín-2020*
|
Dear all.
I'm using your Nanocaller tool in my Pacbio data. However I'm facing some issues related with the -end flag.
Currently Im planning to extract all SNPs and Indel from a bam file derived from CCS_reads aligned to contigs assembly. Despite the --end flag being optional, the tool is asking me to define this -end flag
How can I fix it?
Thanks for the help
The text was updated successfully, but these errors were encountered: