Closed sneha1201 closed 2 years ago
Too few information to reproduce the error. Can you post the complete stack trace?
below mentioned is all which i get after running
Traceback (most recent call last):
File "main.py", line 83, in
Thanks. Looks like you don't have 'trainnucl' key in your conf file.
This file contains the nucleosome profiles for the genomes in the training set.
Try adding that key to your conf file (in the current master branch is commented out)
[default] samtools=samtools nucltemplate : nucl_track trainref=/home/Deeksha/mdlab/storage/data_nice/seqff_reference_sanefalcon.csv
[folders] data=/home/Deeksha/GM01/GM01_C/bamfiles rsp=/home/Deeksha/mdlab/storage/sanefalcon/rsp train=/home/Deeksha/mdlab/storage/sanefalcon/training profiles=/home/Deeksha/mdlab/storage/sanefalcon/training/profiles test=/home/Deeksha/mdlab/storage/sanefalcon/testing testprofiles=/home/Deeksha/mdlab/storage/sanefalcon/testing/profiles listtestingdir=/home/Deeksha/mdlab/storage/data_nice/list_testing_sanefalcon
[training] batchsize=1
This is my configure file . where i need to add keytyoe ?
and also did you know about this seqff_reference_sanefalcon.csv trainref file ? from where it is generated ?
You need to add this in the 'default'
section, as the error suggests. Take a look at the sanefalcon.conf
file in the master
branch.
As for the seqff_reference_sanefalcon.csv
this is something the is not generated, you need to use your own, depending on your cohorte, your methodology, and the reference you want to use.
In our experiments, we wanted to test the fetal fraction computed by iSanefalcon
with respect to seqff
, which was used in clinical trials in the past years for the cohorte on which we were working on.
Hello,
Will you tell me the format for seqff_reference_sanefalcon.csv file , or guide me how to prepare the same .
i tried seqff , but there's no manual there how to use it . if you can guide me with this it will be a great help.
Thanks in advance.
As you may see from its usage, the reference file is a simple csv in the form:
sample1.bam 10.2953 Female
sample2.bam 17.7723 Female
sample3.bam 14.0203 Male
containing three columns, (1) the name of the file, (2) the ff fraction % and (3) the sex of the fetus.
Basically it's a summary of what your other method found (in this case seqff
).
Speaking of which, I do not maintain seqff
, so a simple google search will do the job (e.g., here)
Thanks for such guidance.
After running seqff R script over one of my sam file i got this result : "SeqFF",0.122891340680309 "Enet",0.0888612161167863 "WRSC",0.156921465243832
is this mean my seqFF value is 12.28 roundoff ?
Yes.
Hello ,
if you can guide me with this , it would be a great help. If we are getting negative value what does it mean .
like i am getting value like this "","x" "SeqFF",NA "Enet",NA "WRSC",-0.567157238232598
what does this signify
Thanks in advance
Hello. Negative values are usually a sign of either bad reference set or a too small dataset. Can you provide more details on your experiment?——-MarcoOn 5 Dec 2022, at 10:19, sneha1201 @.***> wrote: Hello , if you can guide me with this , it would be a great help. If we are getting negative value what does it mean . like i am getting value like this "","x" "SeqFF",NA "Enet",NA "WRSC",-0.567157238232598 what does this signify Thanks in advance
—Reply to this email directly, view it on GitHub, or unsubscribe.You are receiving this because you modified the open/close state.Message ID: @.***>
Hello,
while running iSanefalcon i am getting below mentioned error
raise KeyError(key)
KeyError: 'trainnucl' if anyone can help me with this it would be a great help . And also seqff_reference_sanefalcon.csv for trainref from where this file is produced.