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|
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From: OWwtgy <Ma...@wi...> - 2018-10-29 00:46:51
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From: g <Ma...@pi...> - 2018-10-27 07:07:52
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From: vg <Pe...@in...> - 2018-10-25 19:15:34
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From: Evie S. <no-...@rm...> - 2018-10-22 06:32:28
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From: Faber, A. <all...@md...> - 2017-12-15 06:44:59
|
Hello, I'm trying to run the ASE analysis on RNASeq data. Can you provide the scripts required to got from GATK ASEReadCounter to the format you require? I went to the Lappalainen Lab website but it was not helpful. Required inputs at the moment are file formats generated from scripts available fromTuuli Lappalainen's lab at NYGC <http://tllab.org/>. Thanks! Allison |
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From: Nicolas L. O. <nic...@un...> - 2017-08-28 23:57:29
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Dear David, I am using your nice tool MAMBA to do ASE analysis after using GATK ASEReadCount and also counts obtained in phASER. My idea is to compare these 2 data sets, and select (extract) alleles significant imbalanced from 2 different tissues, in 3 different time of development some fishes. I basically have a similar question to others post in the help list, about what to use in the column Exon info when this is “unknown"? I tried several things but always have the same error. Then, also could you explain me (or indicate where to look at), to understand which the —grep command can be used, for me is not clear. Thanks in advance, Regards, Nicolás Lichilín —0— Nicolás Lichilín Ortiz University of Basel Zoological Institute Vesalgasse 1 CH-4051 Basel Switzerland |
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From: Komal R. <kom...@gm...> - 2017-07-12 19:14:59
|
Hi, I have followed these instructions to install mamba: # instructions to install mamba-1.0.0 (http://www.well.ox.ac.uk/~rivas/mamba/) source activate py27 export MAMBA=/home/rathik/tools/miniconda3/envs/py27/bin/ export PYTHONPATH=/home/rathik/tools/miniconda3/envs/py27/bin/ export PYTHONPATH=$PYTHONPATH:/home/rathik/tools/miniconda3/envs/py27/lib/python2.7/site-packages wget http://pypi.python.org/packages/2.7/s/setuptools/setuptools-0.6c11-py2.7.egg; sh setuptools-0.6c11-py2.7.egg --install-dir=$MAMBA; export LD_LIBRARY_PATH=/mnt/isilon/cbmi/variome/bin/mamba-1.0.0/python/dist/:${LD_LIBRARY_PATH}; ./configure --prefix=/home/rathik/tools/miniconda3/envs/py27/; make clean make make install export PATH=$MAMBA:${PATH}; I can now do mamba -h and see all the options. However, I get an error when I type this: mamba --module ASE --fileout input.txt --nt [1] --grep "include|exclude|freqthreshold" Traceback (most recent call last): File "/home/rathik/tools/miniconda3/envs/py27/bin/mamba", line 8, in <module> load_entry_point('mamba==1.0.0', 'console_scripts', 'mamba')() File "build/bdist.linux-x86_64/egg/mamba/MAMBAWrapper.py", line 210, in main File "build/bdist.linux-x86_64/egg/mamba/MAMBAWrapper.py", line 280, in checkArgs File "build/bdist.linux-x86_64/egg/mamba/ASE.py", line 35, in <module> ImportError: No module named rpy.common Please assist. Thanks, Komal |
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From: Rathi, K. S <RA...@EM...> - 2017-07-12 16:49:33
|
Hi, I am trying to install mamba like this: # current working directory $ pwd /mnt/isilon/cbmi/variome/bin/mamba-1.0.0 $ ls bin config.h.in configure INSTALL listDepends.r mkinstalldirs Rdepends.lst CHANGES config.log delete install-sh Makefile python setuptools-0.6c11-py2.7.egg config.h config.status ensureDepend.r list Makefile.in R # follow instructions to install $ export MAMBA=/mnt/isilon/cbmi/variome/bin/mamba-1.0.0/bin/ $ export PYTHONPATH=$PYTHONPATH:/home/rathik/tools/miniconda3/envs/py27/lib/python2.7/site-packages $ source activate py27 # activate python 2.7 env $ wget http://pypi.python.org/packages/2.7/s/setuptools/setuptools-0.6c11-py2.7.egg; $ sh setuptools-0.6c11-py2.7.egg --install-dir=$MAMBA; TEST FAILED: /mnt/isilon/cbmi/variome/bin/mamba-1.0.0/bin/ does NOT support .pth files error: bad install directory or PYTHONPATH You are attempting to install a package to a directory that is not on PYTHONPATH and which Python does not read ".pth" files from. The installation directory you specified (via --install-dir, --prefix, or the distutils default setting) was: /mnt/isilon/cbmi/variome/bin/mamba-1.0.0/bin/ and your PYTHONPATH environment variable currently contains: '' Here are some of your options for correcting the problem: * You can choose a different installation directory, i.e., one that is on PYTHONPATH or supports .pth files * You can add the installation directory to the PYTHONPATH environment variable. (It must then also be on PYTHONPATH whenever you run Python and want to use the package(s) you are installing.) * You can set up the installation directory to support ".pth" files by using one of the approaches described here: http://peak.telecommunity.com/EasyInstall.html#custom-installation-locations Please make the appropriate changes for your system and try again. I am getting the above error. Can you please assist me here. Thanks, -- Komal S. Rathi Bioinformatics Scientist II Department of Biomedical and Health Informatics The Children’s Hospital of Philadelphia |
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From: Rathi, K. S <RA...@EM...> - 2017-07-12 15:50:32
|
Hi all, This is GATK ASEReadCounter output: contig position variantID refAllele altAllele refCount altCount totalCount lowMAPQDepth lowBaseQDepth rawDepth otherBases improperPairs chr2 38021 rs113895774 C T 0 1 1 0 0 1 0 0 chr2 217334 rs6709534 G C 0 3 3 0 0 3 0 0 chr2 218386 rs9213 G A 84 101 185 0 0 185 0 0 chr2 220889 rs3828165 G A 9 7 16 0 0 16 0 0 chr2 221560 rs60484953 G A 11 11 22 0 0 22 0 0 chr2 221981 rs3791224 C T 3 4 7 0 0 7 0 0 chr2 222336 rs3791223 T C 3 8 11 0 0 11 0 0 chr2 224086 rs1474053 T A 3 2 5 0 0 5 0 0 chr2 224919 rs2290911 A G 55 16 71 0 0 71 0 0 The GATK ASEReadCounter manual says that mamba can use this file format as input. However, on mamba’s manual page I read that it requires some additional fields like EXON_INFO - variant annotation label. Can you tell me if mamba can really take GATK ASEReadCounter output file as input? Thanks, Komal |
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From: Nima R. <nim...@gm...> - 2017-04-20 13:35:58
|
Dear Manuel,
I followed all the steps described in installation section. I had to do
some tweeks (because of permission,...) At the end managed to run "make
install" and build bin directory hwere I have executive version of mamba.
But when I run it I get this error:
Traceback (most recent call last):
File "bin/mamba", line 5, in <module>
from pkg_resources import load_entry_point
File
"/pica/v18/b2015317_nobackup/private/UserDirectories/nima/Salinity/ASE/ASEReadCounter/mamba-1.0.0/setuptools-0.6c11-py2.7.egg/pkg_resources.py",
line 2603, in <module>
File
"/pica/v18/b2015317_nobackup/private/UserDirectories/nima/Salinity/ASE/ASEReadCounter/mamba-1.0.0/setuptools-0.6c11-py2.7.egg/pkg_resources.py",
line 666, in require
File
"/pica/v18/b2015317_nobackup/private/UserDirectories/nima/Salinity/ASE/ASEReadCounter/mamba-1.0.0/setuptools-0.6c11-py2.7.egg/pkg_resources.py",
line 565, in resolve
pkg_resources.DistributionNotFound: mamba==1.0.0
Do you know where I am doing something wrong?
Thanks.
Nima
|
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From: Ernst T. <Ern...@cr...> - 2017-03-23 16:47:50
|
Dear MAMBA devs,
I'm running some comparative ASE experiment, and I've seem to run into some
troubles with the usage of the MAMBA ASE module.
The example usage does not clearly state the usage of ASE module, and more
importanlty, the required input format or parameters, is there a manual
available ? I only found the R data from Matti Pirinen's Software
I've tried different parameters, but the only feedback from the software is
: ImportError: ..anaconda2/lib/libreadline.so.6: undefined symbol: PC
My question concerns the usage of GATKs ASEreadcounter output formats. GATK
references your software suit for downstream analysis. Are there conversion
specifcations ?
One minor comments:
your installation instructions on setuptools can be replaced with :
easy_install setuptools
the current instructions produce the error below:
Best wishes,
Ernst
export MAMBA=/home/ethur/anaconda2/bin/;
export
PYTHONPATH=/home/ethur/anaconda2/lib/python2.7/site-packages/:${PYTHONPATH};
sh setuptools-0.6c11-py2.7.egg --install-dir=$MAMBA;
You are attempting to install a package to a directory that is not
on PYTHONPATH and which Python does not read ".pth" files from. The
installation directory you specified (via --install-dir, --prefix, or
the distutils default setting) was:
/home/ethur/anaconda2/bin/
and your PYTHONPATH environment variable currently contains:
'/home/ethur/anaconda2/lib/python2.7/site-packages/:'
|
|
From: Ulrich, A. <ann...@im...> - 2017-02-06 17:36:39
|
Dear Manuel, I have been trying to analyse a small set of rare variants in a cohort of Parkinson`s disease patients but my output files contain only the header and I get no error message just a log file which I cannot make sense of. My plinkseq project contains plink binary files, no VCFs. I will copy my script here: module load mamba/1.0.0 mamba --project PD_proj --locdb /project/silk/users/au615/PD_all/hg19/locdb --seqdb /project/silk/users/au615/PD_all/hg19/seqdb.hg19 --mask all.group reg=chr12:123262000..123300000 --phenotype PD --perm 1 --a 1.5 --t .7 --module SEMGEM --fileout /project/silk/users/au615/PD_all/testSEMGEM And the content of the logfile: 2017-02-06 17:18:11,101 - INFO - Argument N: None 2017-02-06 17:18:11,101 - INFO - Argument Q: False 2017-02-06 17:18:11,101 - INFO - Argument R: False 2017-02-06 17:18:11,101 - INFO - Argument Sigma: None 2017-02-06 17:18:11,101 - INFO - Argument T: False 2017-02-06 17:18:11,101 - INFO - Argument Vp: None 2017-02-06 17:18:11,102 - INFO - Argument a: '1.5' 2017-02-06 17:18:11,102 - INFO - Argument amv: False 2017-02-06 17:18:11,102 - INFO - Argument burn: 1000 2017-02-06 17:18:11,102 - INFO - Argument case: 2 2017-02-06 17:18:11,102 - INFO - Argument covariates: '' 2017-02-06 17:18:11,102 - INFO - Argument delta: None 2017-02-06 17:18:11,102 - INFO - Argument fileout: '/project/silk/users/au615/PD_all/testSEMGEM' 2017-02-06 17:18:11,102 - INFO - Argument filterfile: 'NA' 2017-02-06 17:18:11,102 - INFO - Argument gene: None 2017-02-06 17:18:11,102 - INFO - Argument grep: False 2017-02-06 17:18:11,102 - INFO - Argument gtexdb: None 2017-02-06 17:18:11,103 - INFO - Argument gtexrpkm: 'None' 2017-02-06 17:18:11,103 - INFO - Argument gwas: False 2017-02-06 17:18:11,103 - INFO - Argument gwasin: 'MAMBA.gwas' 2017-02-06 17:18:11,103 - INFO - Argument indep: False 2017-02-06 17:18:11,103 - INFO - Argument locdb: '/project/silk/users/au615/PD_all/hg19/locdb' 2017-02-06 17:18:11,103 - INFO - Argument loci: 1 2017-02-06 17:18:11,103 - INFO - Argument locset: 'refseq' 2017-02-06 17:18:11,103 - INFO - Argument mafiles: None 2017-02-06 17:18:11,103 - INFO - Argument mask: 'all.group' 2017-02-06 17:18:11,103 - INFO - Argument minrpkm: -10000 2017-02-06 17:18:11,103 - INFO - Argument module: 'SEMGEM' 2017-02-06 17:18:11,103 - INFO - Argument monogenic: False 2017-02-06 17:18:11,104 - INFO - Argument monogenicin: 'MAMBA.monogenic' 2017-02-06 17:18:11,104 - INFO - Argument ncpu: 1 2017-02-06 17:18:11,104 - INFO - Argument niter: 4000 2017-02-06 17:18:11,104 - INFO - Argument nt: 0 2017-02-06 17:18:11,104 - INFO - Argument nvars: None 2017-02-06 17:18:11,104 - INFO - Argument outputdir: '.' 2017-02-06 17:18:11,104 - INFO - Argument perms: '1' 2017-02-06 17:18:11,104 - INFO - Argument phenfile: None 2017-02-06 17:18:11,104 - INFO - Argument phenotype: 'PD' 2017-02-06 17:18:11,104 - INFO - Argument pipeline: ['SEMGEM'] 2017-02-06 17:18:11,104 - INFO - Argument plot: False 2017-02-06 17:18:11,105 - INFO - Argument project: 'PD_proj' 2017-02-06 17:18:11,105 - INFO - Argument protdb: None 2017-02-06 17:18:11,105 - INFO - Argument pvalthr: 0.001 2017-02-06 17:18:11,105 - INFO - Argument refdb: None 2017-02-06 17:18:11,105 - INFO - Argument rpkmplots: False 2017-02-06 17:18:11,105 - INFO - Argument rr: 4 2017-02-06 17:18:11,105 - INFO - Argument sample: False 2017-02-06 17:18:11,105 - INFO - Argument seed: False 2017-02-06 17:18:11,105 - INFO - Argument seqdb: '/project/silk/users/au615/PD_all/hg19/seqdb.hg19' 2017-02-06 17:18:11,105 - INFO - Argument strata: False 2017-02-06 17:18:11,105 - INFO - Argument t: '.7' 2017-02-06 17:18:11,105 - INFO - Argument tissue: False 2017-02-06 17:18:11,106 - INFO - Argument two_sided: False 2017-02-06 17:18:11,106 - INFO - Argument vcfs: None 2017-02-06 17:18:11,106 - INFO - Argument verbosity: 'INFO' 2017-02-06 17:18:11,106 - INFO - Argument version: False 2017-02-06 17:18:11,106 - INFO - Running module SEMGEM I hope you can spot the problem easily, I will keep on trying in the meantime, thank you very much for your help. Kind regards, Anna |
|
From: M. J. T. I. <mj...@ud...> - 2017-01-13 16:16:48
|
Dear Manuel A. Rivas, Currently, we are trying to install MAMBA onto a HPC system called BioMix at the University of Delaware, USA. It appears when we try to install/run MAMBA there are module/package conflicts. Message from Karol Maskiewicz (cc'ed on this email) who is the Manager of the HPC system and who is installing MAMBA because of all the software requirements. "The problem is with Python's rpy2 module. Essentially, this module, which communicates/uses R, does not work correctly. I've found similar reports concerning rpy2 on-line. Unfortunately, there does not seem to by any clear-cut solution offered to solve the problem. Essentially, it comes to interaction and lack of some compatibility between system libraries (most point to readline library), R, and Python module." I was hoping you might be able to offer some suggestions on the installation process. I have also included my qsub scripts, data used (test set from website) and all output messages, in case you need to see that information to know the exact problem. If you need any further information, please feel free to contact me. Thank You, M. Joseph Tomlinson IV |
|
From: ASCIA E. <as...@uc...> - 2016-09-20 02:08:03
|
Hi, I am using mamba with output from GATK ASEReadCounter. I don't know the Exon Info. I was trying to run the software, but was having errors due to the grep command. If I make the Exon Info "SEVERE_IMPACT=STOP_GAINED" and use the grep command in the example --grep ">,0,=STOP_GAINED|DFGFDG" it works. What grep command should I use for "Unkown"? Or is it ok to leave the exon information as is? (more sever than it actually might be.) Does it affect the output? Best, Ascia |
|
From: Nathan A. H. <nha...@st...> - 2016-06-01 03:45:00
|
Hello, I was just installing Mamba based on the instructions on this page: http://www.well.ox.ac.uk/~rivas/mamba/ The link for required dependency PyPLINK/SEQ is dead, and I wasn’t able to find that software elsewhere. Is it sill possible to install Mamba? Any help is appreciated. Best, Nathan — Nathan Hammond, PhD Senior Software Engineer Stanford Center for Genomics and Personalized Medicine 617-501-0529 |
|
From: Gaurav T. <gau...@gm...> - 2016-03-09 11:41:35
|
Dear All, I am trying to run Mamba on European ancestry samples from Geuvadis RNA-Seq data. I have created a file with heterozygous variant calls from RNA seq data and converted into mamba format. But as the dataset contain only single tissue, should the heterozygous sites used in the analysis be from DNA seq data or RNA seq data? Thank you for your help. Regards Gaurav Thareja |
|
From: Szabolcs S. <ssz...@tg...> - 2016-03-03 23:11:04
|
Hi, I am completely new to MAMBA and trying to figure out how you make NMD prediction work. Reading getpredictors.py script, I find that the 4th argument is the the input file for which NMD should be predicted. Could you explain how you generate the input for this script? What is includes and in what format. This is all I find in the script ## Variants to predict NMD ## Format: chr:pos ref alt af lofflag trnscaffected Is this input file tab delimited or space? is the lofflag numerical (0,1,2) or a character string (ie. nonsense, splice-site) is trnscaffected numerical (0,1,2) or a charctare string (ie. FULL, PARTIAL) In addition, once the output file is created, would it become the input to the R predition script as newdata= ? predict(modelFit.RF,newdata=tmp.data,type="prob",na.action=na.roughfix) Thanks for your input, Szabi Szabolcs Szelinger Research Associate Neurogenomics Division, The Translational Genomics Research Institute (TGen) 445 N. 5th Street, Phoenix AZ 85044 ph:602-343-8723 ssz...@tg...<mailto:ssz...@tg...> ________________________________ ________________________________ This electronic message is intended to be for the use only of the named recipient, and may contain information that is confidential or privileged, including patient health information. If you are not the intended recipient, you are hereby notified that any disclosure, copying, distribution or use of the contents of this message is strictly prohibited. If you have received this message in error or are not the named recipient, please notify us immediately by contacting the sender at the electronic mail address noted above, and delete and destroy all copies of this message. Thank you. |
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From: Taina F. <tai...@cr...> - 2016-03-02 18:09:30
|
Good night Dr. Rivas, I'm Taina Figueiredo, pHD student on Universitat Autònoma de Barcelona. I`m work with RNA-Seq and I want to see the allele specific expression in my data. I installed the MAMBA and all dependence, but when I tried to run a test, I have this message: antonia@pc-249:~/allelic/MAMBA/mamba-1.0.0$ mamba --project mambaproj --locdb /PATH/TO/locdb --seqdb /PATH/TO/seqdb --mask "loc.group=refseq" --locset refseq --phenotype phe --perm 1 --a 1.5 --t .7 --module SEMGEM --fileout testSEMGEM No command 'mamba' found, did you mean: Command 'samba' from package 'samba' (main) mamba: command not found Can you help me? Thank you in advance. Tainã Figueiredo Cardoso, PhD Student Universitat Autònoma de Barcelona Animal Genetics Centre for Research in Agricultural Genomics (CRAG) Consorci CSIC-IRTA-UAB Campus UAB Edifici CRAG Bellaterra (Cerdanyola del Vallés) 08193 Barcelona - Spain Phone: +34 93 563 6600 Extension: 3349 |
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From: Alexandros D. <dim...@fl...> - 2015-10-05 13:49:35
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Thank you for your help! On 04/10/15 11:31, Manuel Rivas wrote: > Hello Alexandros - Please read the following section: > > > Application to simulated dataset. > > We simulated ASE data for 300 variants and 3 tissues. RNA-seq coverage > is simulated as a Poisson distribution > <http://en.wikipedia.org/wiki/Poisson_distribution> with expected > coverage of 30,20, and 40 for each tissue. > > A 67%, 23%, 10% mixture dataset with θ= .8, .5, .95 (binomial > distribution <http://en.wikipedia.org/wiki/Binomial_distribution>) was > generated. > > To apply the models we run mamba as follows > > mamba --module ASE --fileout asetest.txt.gz --nt 2 --seed 10 --grep ">,0,=STOP_GAINED|DFGFDG" --niter 100 --burn 10 > > where |--niter [int]| and |--burn [int]| are the number of iterations > and burn-in period for the Gibbs sampler, respectively. > > Results from the GTM and the GTM* (when multiple tissues are > available) are generated. GTM estimates: > > NOASE MODASE SNGASE HET0 HET1 > 1 0.2166671 0.6467365 0.08923985 0.02666694 0.02068966 > Whereas GTM* estimates: > est low95 up95 > NOASE 0.226645280 0.1887562079 0.27998550 > MODASE 0.664520022 0.5992223252 0.71721846 > SNGASE 0.094709155 0.0621824885 0.12861006 > HET0 0.004789438 0.0001708784 0.01900929 > HET1 0.009336103 0.0004127940 0.03151795 > with tissue-specificity estimate: > est low95 up95 > TIS_SPE 0.006466667 0.00 0.01553708 > > On Thu, Oct 1, 2015 at 5:23 AM, Alexandros Dimopoulos > <dim...@fl... <mailto:dim...@fl...>> wrote: > > Dear Dr. Rivas, > > After using the GATK ASEReadCounter walker on my data, I was > directed to > the MAMBA software for allele-specific expression analysis. > I have downloaded and successfully installed MAMBA but I cannot > make it > execute the ASE example. I have downloaded both the small > asetest.txt.gz > example and the much larger GEUVADIS ASE file > GD462.ASE.COV8.ANNOT_PTV.txt.gz. However, when I give the command > > mamba --module ASE --fileout asetest.txt.gz --nt 1 --grep > "include|exclude|freqthreshold" --verbosity CRITICAL > > I get an error: > > /home/dimopoulos/anaconda/lib/python2.7/site-packages/pandas/rpy/__init__.py:11: > FutureWarning: The pandas.rpy module is deprecated and will be removed > in a future version. We refer to external packages like rpy2. > See here for a guide on how to port your code to rpy2: > http://pandas.pydata.org/pandas-docs/stable/r_interface.html > FutureWarning) > Traceback (most recent call last): > File "/home/dimopoulos/anaconda/bin/mamba", line 8, in <module> > load_entry_point('mamba==1.0.0', 'console_scripts', 'mamba')() > File "build/bdist.linux-x86_64/egg/mamba/MAMBAWrapper.py", line > 214, > in main > File "build/bdist.linux-x86_64/egg/mamba/MAMBAWrapper.py", line > 249, > in runModule > File "build/bdist.linux-x86_64/egg/mamba/ASE.py", line 969, in main > ValueError: could not convert string to float: freqthreshold > > if I remove the --grep "include|exclude|freqthreshold" part of the > command I still get an error: > > mamba --module ASE --fileout asetest.txt.gz --nt 1 --verbosity > CRITICAL > > /home/dimopoulos/anaconda/lib/python2.7/site-packages/pandas/rpy/__init__.py:11: > FutureWarning: The pandas.rpy module is deprecated and will be removed > in a future version. We refer to external packages like rpy2. > See here for a guide on how to port your code to rpy2: > http://pandas.pydata.org/pandas-docs/stable/r_interface.html > FutureWarning) > Traceback (most recent call last): > File "/home/dimopoulos/anaconda/bin/mamba", line 8, in <module> > load_entry_point('mamba==1.0.0', 'console_scripts', 'mamba')() > File "build/bdist.linux-x86_64/egg/mamba/MAMBAWrapper.py", line > 214, > in main > File "build/bdist.linux-x86_64/egg/mamba/MAMBAWrapper.py", line > 249, > in runModule > File "build/bdist.linux-x86_64/egg/mamba/ASE.py", line 947, in main > AttributeError: 'bool' object has no attribute 'split' > > Do you have any suggestions on what I might be doing wrong? > > Thank you in advance for your time, > > Alexandros Dimopoulos > > Post Doctoral Fellow > Biomedical Sciences Research Center “Alexander Fleming” > Institute of Molecular Biology & Genetics > Vari, 16672 > Athens, Greece > +30-210-9656310 (ext. 144) > > > > > > > ------------------------------------------------------------------------------ > _______________________________________________ > mambas-help mailing list > mam...@li... > <mailto:mam...@li...> > https://lists.sourceforge.net/lists/listinfo/mambas-help > > |
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From: Manuel R. <mar...@gm...> - 2015-10-04 08:31:20
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Hello Alexandros - Please read the following section: Application to simulated dataset. We simulated ASE data for 300 variants and 3 tissues. RNA-seq coverage is simulated as a Poisson distribution <http://en.wikipedia.org/wiki/Poisson_distribution> with expected coverage of 30,20, and 40 for each tissue. A 67%, 23%, 10% mixture dataset with θ= .8, .5, .95 (binomial distribution <http://en.wikipedia.org/wiki/Binomial_distribution>) was generated. To apply the models we run mamba as follows mamba --module ASE --fileout asetest.txt.gz --nt 2 --seed 10 --grep ">,0,=STOP_GAINED|DFGFDG" --niter 100 --burn 10 where --niter [int] and --burn [int] are the number of iterations and burn-in period for the Gibbs sampler, respectively. Results from the GTM and the GTM* (when multiple tissues are available) are generated. GTM estimates: NOASE MODASE SNGASE HET0 HET1 1 0.2166671 0.6467365 0.08923985 0.02666694 0.02068966 Whereas GTM* estimates: est low95 up95 NOASE 0.226645280 0.1887562079 0.27998550 MODASE 0.664520022 0.5992223252 0.71721846 SNGASE 0.094709155 0.0621824885 0.12861006 HET0 0.004789438 0.0001708784 0.01900929 HET1 0.009336103 0.0004127940 0.03151795 with tissue-specificity estimate: est low95 up95 TIS_SPE 0.006466667 0.00 0.01553708 On Thu, Oct 1, 2015 at 5:23 AM, Alexandros Dimopoulos <dim...@fl... > wrote: > Dear Dr. Rivas, > > After using the GATK ASEReadCounter walker on my data, I was directed to > the MAMBA software for allele-specific expression analysis. > I have downloaded and successfully installed MAMBA but I cannot make it > execute the ASE example. I have downloaded both the small asetest.txt.gz > example and the much larger GEUVADIS ASE file > GD462.ASE.COV8.ANNOT_PTV.txt.gz. However, when I give the command > > mamba --module ASE --fileout asetest.txt.gz --nt 1 --grep > "include|exclude|freqthreshold" --verbosity CRITICAL > > I get an error: > > > /home/dimopoulos/anaconda/lib/python2.7/site-packages/pandas/rpy/__init__.py:11: > FutureWarning: The pandas.rpy module is deprecated and will be removed > in a future version. We refer to external packages like rpy2. > See here for a guide on how to port your code to rpy2: > http://pandas.pydata.org/pandas-docs/stable/r_interface.html > FutureWarning) > Traceback (most recent call last): > File "/home/dimopoulos/anaconda/bin/mamba", line 8, in <module> > load_entry_point('mamba==1.0.0', 'console_scripts', 'mamba')() > File "build/bdist.linux-x86_64/egg/mamba/MAMBAWrapper.py", line 214, > in main > File "build/bdist.linux-x86_64/egg/mamba/MAMBAWrapper.py", line 249, > in runModule > File "build/bdist.linux-x86_64/egg/mamba/ASE.py", line 969, in main > ValueError: could not convert string to float: freqthreshold > > if I remove the --grep "include|exclude|freqthreshold" part of the > command I still get an error: > > mamba --module ASE --fileout asetest.txt.gz --nt 1 --verbosity CRITICAL > > > /home/dimopoulos/anaconda/lib/python2.7/site-packages/pandas/rpy/__init__.py:11: > FutureWarning: The pandas.rpy module is deprecated and will be removed > in a future version. We refer to external packages like rpy2. > See here for a guide on how to port your code to rpy2: > http://pandas.pydata.org/pandas-docs/stable/r_interface.html > FutureWarning) > Traceback (most recent call last): > File "/home/dimopoulos/anaconda/bin/mamba", line 8, in <module> > load_entry_point('mamba==1.0.0', 'console_scripts', 'mamba')() > File "build/bdist.linux-x86_64/egg/mamba/MAMBAWrapper.py", line 214, > in main > File "build/bdist.linux-x86_64/egg/mamba/MAMBAWrapper.py", line 249, > in runModule > File "build/bdist.linux-x86_64/egg/mamba/ASE.py", line 947, in main > AttributeError: 'bool' object has no attribute 'split' > > Do you have any suggestions on what I might be doing wrong? > > Thank you in advance for your time, > > Alexandros Dimopoulos > > Post Doctoral Fellow > Biomedical Sciences Research Center “Alexander Fleming” > Institute of Molecular Biology & Genetics > Vari, 16672 > Athens, Greece > +30-210-9656310 (ext. 144) > > > > > > > > ------------------------------------------------------------------------------ > _______________________________________________ > mambas-help mailing list > mam...@li... > https://lists.sourceforge.net/lists/listinfo/mambas-help > |
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From: Alexandros D. <dim...@fl...> - 2015-10-01 09:54:45
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Dear Dr. Rivas, After using the GATK ASEReadCounter walker on my data, I was directed to the MAMBA software for allele-specific expression analysis. I have downloaded and successfully installed MAMBA but I cannot make it execute the ASE example. I have downloaded both the small asetest.txt.gz example and the much larger GEUVADIS ASE file GD462.ASE.COV8.ANNOT_PTV.txt.gz. However, when I give the command mamba --module ASE --fileout asetest.txt.gz --nt 1 --grep "include|exclude|freqthreshold" --verbosity CRITICAL I get an error: /home/dimopoulos/anaconda/lib/python2.7/site-packages/pandas/rpy/__init__.py:11: FutureWarning: The pandas.rpy module is deprecated and will be removed in a future version. We refer to external packages like rpy2. See here for a guide on how to port your code to rpy2: http://pandas.pydata.org/pandas-docs/stable/r_interface.html FutureWarning) Traceback (most recent call last): File "/home/dimopoulos/anaconda/bin/mamba", line 8, in <module> load_entry_point('mamba==1.0.0', 'console_scripts', 'mamba')() File "build/bdist.linux-x86_64/egg/mamba/MAMBAWrapper.py", line 214, in main File "build/bdist.linux-x86_64/egg/mamba/MAMBAWrapper.py", line 249, in runModule File "build/bdist.linux-x86_64/egg/mamba/ASE.py", line 969, in main ValueError: could not convert string to float: freqthreshold if I remove the --grep "include|exclude|freqthreshold" part of the command I still get an error: mamba --module ASE --fileout asetest.txt.gz --nt 1 --verbosity CRITICAL /home/dimopoulos/anaconda/lib/python2.7/site-packages/pandas/rpy/__init__.py:11: FutureWarning: The pandas.rpy module is deprecated and will be removed in a future version. We refer to external packages like rpy2. See here for a guide on how to port your code to rpy2: http://pandas.pydata.org/pandas-docs/stable/r_interface.html FutureWarning) Traceback (most recent call last): File "/home/dimopoulos/anaconda/bin/mamba", line 8, in <module> load_entry_point('mamba==1.0.0', 'console_scripts', 'mamba')() File "build/bdist.linux-x86_64/egg/mamba/MAMBAWrapper.py", line 214, in main File "build/bdist.linux-x86_64/egg/mamba/MAMBAWrapper.py", line 249, in runModule File "build/bdist.linux-x86_64/egg/mamba/ASE.py", line 947, in main AttributeError: 'bool' object has no attribute 'split' Do you have any suggestions on what I might be doing wrong? Thank you in advance for your time, Alexandros Dimopoulos Post Doctoral Fellow Biomedical Sciences Research Center “Alexander Fleming” Institute of Molecular Biology & Genetics Vari, 16672 Athens, Greece +30-210-9656310 (ext. 144) |
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From: Manuel R. <mar...@gm...> - 2015-09-02 18:41:49
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Dear Kyu-Tae - many thanks for your e-mail. Can you e-mail me a short snippet of what allele_count.txt looks like so that I can assist you in getting the format right. Best Regards, Manuel On Wed, Aug 12, 2015 at 7:51 AM, Kyu-Tae Kim <thi...@gm...> wrote: > Dear Dr.Rivas, > > It was great to know how genetic variants affect transcriptional dynamics > from your substantial efforts with GTEx consortium that have been reported > in Science, 2015. > > I'm Kyu-Tae Kim from Samsung Medical Center (Korea) and studying cancer > genomics. > > One of my study is to address the link between ASE and intratumoral > heterogenity. > I tried to get ASE pattern by implementing mamba but the overall process > of your approach is not clear to me. > I installed or downloaded related tools or scripts including mamba, > GATK3.4 and Lappalainen's scripts (downloaded from her lab homepage). > Can you explain more detailed for how I could analyze ASE? > > My previous attempts to follow the instruction of 'mamba' has been just at > the first stage. > > 1. ASEReadCounter (from GATK 3.4): .vcf --> allele_count.txt > > I'm not sure the next step with the allele_count.txt data. > It would be wonderful if you help me understand clearer. > > Thank you very much. > > Sincerely, > Kyu-Tae Kim > > > > |
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From: Kyu-Tae K. <thi...@gm...> - 2015-08-12 11:51:41
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Dear Dr.Rivas, It was great to know how genetic variants affect transcriptional dynamics from your substantial efforts with GTEx consortium that have been reported in Science, 2015. I'm Kyu-Tae Kim from Samsung Medical Center (Korea) and studying cancer genomics. One of my study is to address the link between ASE and intratumoral heterogenity. I tried to get ASE pattern by implementing mamba but the overall process of your approach is not clear to me. I installed or downloaded related tools or scripts including mamba, GATK3.4 and Lappalainen's scripts (downloaded from her lab homepage). Can you explain more detailed for how I could analyze ASE? My previous attempts to follow the instruction of 'mamba' has been just at the first stage. 1. ASEReadCounter (from GATK 3.4): .vcf --> allele_count.txt I'm not sure the next step with the allele_count.txt data. It would be wonderful if you help me understand clearer. Thank you very much. Sincerely, Kyu-Tae Kim |