Comments (10)
Hello Dr.Chen,
I saw the latest update version of the Combine_VCF_files.pl. Thank you so much for your help! Really appreciate!
Best,
Yaaoo
from ervcaller.
Hi,
could you provide more info how you get your output vcf? like what parameters you used to get it?
you are correct, insertions within a small window (e.g., 1500bp) will be merged. Regarding the insertions on chr19, I don't know what happened so far without more info. Is it a singleton? low quality? However, I think we did not filter low-quality loci in the combined script.
Best,
Xun
from ervcaller.
Hello,
I have figured out the problem about "GQ" value in output.vcf. ~ But still are confused with merge step. Here are one output.vcf of my samples and my merge_output.vcf. I think the insertions with red marks also should be included in the merge.vcf, while they were not. And this missing situation happened in every input sample. what might lead to this problem~? (last one is my merge.vcf)
Thank you for your reply!
from ervcaller.
Hi,
Can you try to sort the individual VCF first before merging? Let me know if it doesn't work. You could also follow our protocol here: https://doi.org/10.1007/978-1-0716-2883-6_4.
Can you also check if you find these missing loci in the file containing consensus TE loci?
Xun
from ervcaller.
Hi, Dr.Chen
I followed the protocol and sorted individual VCF files before the merging step, but it didn't work. And the txt.consensus file did not contain those missing loci. What might cause this problem?~
Thank you!
from ervcaller.
Do you want to attach some example VCF files containing the problematic loci? I could help debug it?
If the consensus txt file does not have it, it should be something to do with either the VCF files or the Combine_VCF_files.pl script.
Best,
Xun
from ervcaller.
Hi,
Here are my example merging.vcf file and two my sample vcf files (AM107 and AM102). My detecting step ran with the parameter "-t 24 -S 40 -r 150 -n 2 -G" and the following steps followed the protocol.
Thank you so much for your reply and help!
from ervcaller.
Hi,
Thanks for sharing the example file and sorry for the wait due to the holiday break.
It was finally resolved and you could download the revised Combine_VCF_files.pl here and replace the original one: https://github.com/xunchen85/ERVcaller/blob/v1.4/Scripts/Combine_VCF_files.pl.
It was due to two bugs here relative to the row end problem and a small number of TE loci (e.g., one TE insertion on an entire chromosome).
ps, let me know if you have further questions!
Best,
Xun
from ervcaller.
Hello Dr.Chen,
Thank you for your reply and help! I tried the new version of Combine_VCF_files.pl and the output merged VCF contained more insertions. But it seemed that the VCF still missed a few insertions. I uploaded some example files here (the merged VCF lacked the 'chr15 63082393' insertion in AM104 and 'chr5 168576151' insertion in AM101). What might cause this ? maybe the special insertion position? ..
example.zip
Thank you so much!
from ervcaller.
Hi,
Thanks for your feedback. It was corrected which was due to a similar bug. You can download the Combine_VCF_files.pl from the same link: https://github.com/xunchen85/ERVcaller/blob/v1.4/Scripts/Combine_VCF_files.pl.
After merging, you will now get 20 unique TE insertion loci. Let me know if you have further questions.
Thanks,
Xun
from ervcaller.
Related Issues (20)
- failed at step 3 HOT 3
- Problem in Step 2 HOT 5
- Error unexpected end of file HOT 1
- RNAseq data HOT 3
- I also had a problem with the second step HOT 10
- [E::bwa_idx_load_from_disk] fail to locate the index files HOT 10
- Cannot remove "sort.bam.tmp.0000.bam" files HOT 2
- bwa-mem2 HOT 2
- Some chromosomes don't harbour any variation HOT 5
- A question about the "INFOR" field HOT 4
- About using TGS data HOT 2
- Some chromosomes don't harbour any variation HOT 2
- Length of TSD HOT 2
- Assembly of the target ERV HOT 1
- Question of setting the -H parameter HOT 1
- A question of filter criteria in guide paper HOT 1
- Error in finding the input data under the provided sampleID HOT 2
- Cannot progress beyond step 2 HOT 5
- Assemble inserted virus sequence through intermediate output files HOT 8
Recommend Projects
-
React
A declarative, efficient, and flexible JavaScript library for building user interfaces.
-
Vue.js
🖖 Vue.js is a progressive, incrementally-adoptable JavaScript framework for building UI on the web.
-
Typescript
TypeScript is a superset of JavaScript that compiles to clean JavaScript output.
-
TensorFlow
An Open Source Machine Learning Framework for Everyone
-
Django
The Web framework for perfectionists with deadlines.
-
Laravel
A PHP framework for web artisans
-
D3
Bring data to life with SVG, Canvas and HTML. 📊📈🎉
-
Recommend Topics
-
javascript
JavaScript (JS) is a lightweight interpreted programming language with first-class functions.
-
web
Some thing interesting about web. New door for the world.
-
server
A server is a program made to process requests and deliver data to clients.
-
Machine learning
Machine learning is a way of modeling and interpreting data that allows a piece of software to respond intelligently.
-
Visualization
Some thing interesting about visualization, use data art
-
Game
Some thing interesting about game, make everyone happy.
Recommend Org
-
Facebook
We are working to build community through open source technology. NB: members must have two-factor auth.
-
Microsoft
Open source projects and samples from Microsoft.
-
Google
Google ❤️ Open Source for everyone.
-
Alibaba
Alibaba Open Source for everyone
-
D3
Data-Driven Documents codes.
-
Tencent
China tencent open source team.
from ervcaller.