[med-svn] [Git][med-team/tnseq-transit][master] 4 commits: New upstream version
Michael R. Crusoe
gitlab at salsa.debian.org
Fri Nov 8 17:14:12 GMT 2019
Michael R. Crusoe pushed to branch master at Debian Med / tnseq-transit
Commits:
6ee16a6c by Michael R. Crusoe at 2019-11-08T17:06:42Z
New upstream version
- - - - -
cad37841 by Michael R. Crusoe at 2019-11-08T17:06:43Z
New upstream version 3.0.1
- - - - -
8b33fcaa by Michael R. Crusoe at 2019-11-08T17:08:33Z
Update upstream source from tag 'upstream/3.0.1'
Update to upstream version '3.0.1'
with Debian dir 0251a39c58d356fe1be830515c91200a50d6a11e
- - - - -
dbc03cfe by Michael R. Crusoe at 2019-11-08T17:11:08Z
removed now-undeeded 2to3.patch
- - - - -
15 changed files:
- CHANGELOG.md
- Dockerfile
- README.md
- debian/changelog
- − debian/patches/2to3.patch
- debian/patches/series
- setup.py
- src/pytpp/__main__.py
- src/pytpp/tpp_tools.py
- src/pytransit/__init__.py
- src/pytransit/__main__.py
- src/pytransit/analysis/gi.py
- − src/pytransit/analysis/multitnseq.py
- − src/pytransit/analysis/multitnseq_helpers.py
- src/pytransit/analysis/pathway_enrichment.py
Changes:
=====================================
CHANGELOG.md
=====================================
@@ -1,6 +1,11 @@
# Change log
All notable changes to this project will be documented in this file.
+## Version 3.0.1 2019-08-01
+#### TRANSIT:
+ - Add check for python3 (TRANSIT 3+ requires python3.6+)
+ - Minor fixes in GI and Pathway Enrichment
+
## Version 3.0.0 2019-07-18
#### TRANSIT:
- TRANSIT now supports python 3. (To use with python 2, use releases < 3.0.0)
=====================================
Dockerfile
=====================================
@@ -1,8 +1,8 @@
-From r-base:3.4.1
-RUN apt-get update -y && apt-get install -y -f python2 python-dev python-pip
+From r-base:3.6.1
+RUN apt-get update -y && apt-get install -y -f python3 python-dev python3-pip
ADD src/ /src
ADD tests/ /tests
-RUN pip install pytest 'numpy~=1.15' 'scipy~=1.2' 'matplotlib~=2.2' 'pillow~=5.0' 'statsmodels~=0.9' 'rpy2<2.9.0'
+RUN pip3 install pytest 'numpy~=1.16' 'scipy~=1.2' 'matplotlib~=3.0' 'pillow~=6.0' 'statsmodels~=0.9' 'rpy2'
RUN R -e "install.packages('MASS')"
RUN R -e "install.packages('pscl')"
=====================================
README.md
=====================================
@@ -1,8 +1,11 @@
# TRANSIT
[](https://github.com/mad-lab/transit) [](https://travis-ci.org/mad-lab/transit) [](http://transit.readthedocs.io/en/latest/?badge=latest) [](https://pepy.tech/project/tnseq-transit)
+
=======
+**NOTE: TRANSIT v3.0+ now requires python3.6+. If you want to use TRANSIT with python2, use version < 3.0.**
+
Welcome! This is the distribution for the TRANSIT and TPP tools developed by the [Ioerger Lab](http://orca2.tamu.edu/tom/iLab.html) at Texas A&M University.
TRANSIT is a tool for processing and statistical analysis of Tn-Seq data.
@@ -22,7 +25,7 @@ TRANSIT offers a variety of features including:
- Ability to analyze datasets from libraries constructed using **himar1 or tn5 transposons**.
-- **TrackView** to help visualize read-counts accross the genome.
+- **TrackView** to help visualize read-counts across the genome.
- Can **export datasets** into a variety of formats, including **IGV**.
=====================================
debian/changelog
=====================================
@@ -1,5 +1,6 @@
-tnseq-transit (3.0.0-1) UNRELEASED; urgency=medium
+tnseq-transit (3.0.1-1) UNRELEASED; urgency=medium
+ [ Andreas Tille ]
* New upstream version
* New version supports Python3
Closes: #931711
@@ -9,6 +10,9 @@ tnseq-transit (3.0.0-1) UNRELEASED; urgency=medium
TODO: https://pypi.org/project/PyPubSub/
-> see new queue (#939493)
+ [ Michael R. Crusoe ]
+ * removed now-undeeded 2to3.patch
+
-- Andreas Tille <tille at debian.org> Thu, 25 Jul 2019 21:35:41 +0200
tnseq-transit (2.5.2-1) unstable; urgency=medium
=====================================
debian/patches/2to3.patch deleted
=====================================
@@ -1,125 +0,0 @@
-Author: Andreas Tille <tille at debian.org>
-Last-Update: Thu, 25 Jul 2019 21:35:41 +0200
-Description: Use 2to3 to finalise Python2 -> Python3 migration
-
---- a/src/pytransit/analysis/multitnseq.py
-+++ b/src/pytransit/analysis/multitnseq.py
-@@ -9,7 +9,7 @@ try:
- except Exception as e:
- hasR = False
-
--import base
-+from . import base
- import numpy
- import scipy
- import pdfkit
-@@ -18,7 +18,7 @@ import statsmodels.stats.multicomp
- import pytransit.transit_tools as transit_tools
- import pytransit.tnseq_tools as tnseq_tools
- import pytransit.norm_tools as norm_tools
--from multitnseq_helpers import def_r_samples_corrplot, def_r_clustering, def_r_make_heatmap, def_r_conditions_corrplot
-+from .multitnseq_helpers import def_r_samples_corrplot, def_r_clustering, def_r_make_heatmap, def_r_conditions_corrplot
-
- ###### GUI ELEMENTS ######
- short_name = "MultiTnSeq"
-@@ -60,7 +60,7 @@ class MultiTnSeqMethod(base.AnalysisMeth
- (args, kwargs) = transit_tools.cleanargs(rawargs)
-
- if (kwargs.get('-help', False) or kwargs.get('h', False)):
-- print(MultiTnSeqMethod.usage_string())
-+ print((MultiTnSeqMethod.usage_string()))
- sys.exit(0)
-
- fna = args[0]
-@@ -130,7 +130,7 @@ class MultiTnSeqMethod(base.AnalysisMeth
- if Samples.get(row,"Condition") == cond:
- fname = Samples.get(row,"Filename")
- if fname not in filenamesInCombWig:
-- print "error: filename '%s' listed in samples metadata not found in combined wig file" % fname; sys.exit(0)
-+ print("error: filename '%s' listed in samples metadata not found in combined wig file" % fname); sys.exit(0)
- SampleIndexes.append(row)
- wigindexes.append(filenamesInCombWig.index(fname))
-
-@@ -149,7 +149,7 @@ class MultiTnSeqMethod(base.AnalysisMeth
- fname = Samples.get(row,"Filename")
- cond2datasets[cond].append(filenamesInData.index(fname))
- if len(cond2datasets[cond]) == 0:
-- print "error: no samples found in metadata for condition %s" % cond; sys.exit(0)
-+ print("error: no samples found in metadata for condition %s" % cond); sys.exit(0)
-
- (normed, factors) = norm_tools.normalize_data(data, method='TTR')
- Nds,Nsites = normed.shape # transposed: rows are datasets, cols are TA sites
-@@ -196,15 +196,15 @@ class MultiTnSeqMethod(base.AnalysisMeth
-
-
- if False: # print means for each gene for each dataset
-- print '\t'.join(filenamesInData)
-- print '\t'.join([Samples.get(x,"Id") for x in SampleIndexes])
-+ print('\t'.join(filenamesInData))
-+ print('\t'.join([Samples.get(x,"Id") for x in SampleIndexes]))
- for (start,end,Rv,gene,strand) in genes:
- if len(TAsites[Rv])>0: # skip genes with no TA sites
- means = []
- for j in range(Nds):
- obs = normed[j,TAsites[Rv]]
- means.append(numpy.mean(obs))
-- print '\t'.join([Rv,gene,str(len(TAsites[Rv]))]+["%0.1f" % x for x in means])
-+ print('\t'.join([Rv,gene,str(len(TAsites[Rv]))]+["%0.1f" % x for x in means]))
- #sys.exit(0)
-
-
-@@ -344,14 +344,14 @@ class MultiTnSeqMethod(base.AnalysisMeth
- batches[batch].append(Means[Rv][r])
- vals.append(Means[Rv][r]) ###
- for b in "CC1 CC2 CC3 KO".split(): vals.append(numpy.mean(batches[b]))
-- print '\t'.join([Rv,gene]+["%0.1f" % x for x in vals]) ###
-+ print('\t'.join([Rv,gene]+["%0.1f" % x for x in vals])) ###
- ###sys.exit(0)
-
-
-
- # remove batch effects (subtract batch means from mean gene counts; adjust each to global mean)
- if self.debatch and "Batch" in Conditions.headers:
-- print "<BR>correcting means for batch effects..."
-+ print("<BR>correcting means for batch effects...")
- for (start,end,Rv,gene,strand) in genes:
- if Rv in Means:
- batches = {}
-@@ -372,11 +372,11 @@ class MultiTnSeqMethod(base.AnalysisMeth
-
- if False: # print gene means for each condition (with batch corrections)
- vals = ['ORF','gene']+Conditions.getcol("Condition")
-- print '\t'.join(vals)
-+ print('\t'.join(vals))
- for (start,end,Rv,gene,strand) in genes:
- if Rv not in Means: continue
- vals = [Means[Rv][r] for r in range(Conditions.nrows)]
-- print '\t'.join([Rv,gene]+["%0.1f" % x for x in vals])
-+ print('\t'.join([Rv,gene]+["%0.1f" % x for x in vals]))
- sys.exit(0)
-
- ################################
-@@ -398,11 +398,11 @@ class MultiTnSeqMethod(base.AnalysisMeth
- lfcs[Rv] = lfcvec
-
- if self.stdnorm:
-- print "<BR>applying standard normalization to LFCs"
-+ print("<BR>applying standard normalization to LFCs")
- for i,cond in enumerate(Conditions.keys):
-- col = [row[i] for row in lfcs.values()]
-+ col = [row[i] for row in list(lfcs.values())]
- m,s = numpy.mean(col),numpy.std(col) # consider using quantiles(col,[0,0.25,0.5,0.75,1.0])
-- for Rv in lfcs.keys():
-+ for Rv in list(lfcs.keys()):
- lfcs[Rv][i] = (lfcs[Rv][i]-m)/s
-
- file = open(self.makefname("temp_LFCs.txt", self.rundir),"w")
-@@ -415,7 +415,7 @@ class MultiTnSeqMethod(base.AnalysisMeth
- file.write('\t'.join([str(x) for x in vals])+EOL)
- cnt += 1
- file.close()
-- if cnt==0: print "error: no significantly varying genes found by ANOVA"; return
-+ if cnt==0: print("error: no significantly varying genes found by ANOVA"); return
-
- r_conditions_corrplot = def_r_conditions_corrplot()
- r_make_heatmap = def_r_make_heatmap()
=====================================
debian/patches/series
=====================================
@@ -1,2 +1 @@
skip_test_requiring_non_existing_input_data.patch
-2to3.patch
=====================================
setup.py
=====================================
@@ -101,6 +101,7 @@ setup(
description='TRANSIT is a tool for the analysis of Tn-Seq data. It provides an easy to use graphical interface and access to three different analysis methods that allow the user to determine essentiality in a single condition as well as between conditions.',
long_description=long_description,
+ long_description_content_type='text/markdown',
# The project's main homepage.
url='https://github.com/mad-lab/transit',
=====================================
src/pytpp/__main__.py
=====================================
@@ -39,6 +39,10 @@ def run_main():
main(*args, **kwargs)
def main(*args, **kwargs):
+ # Check python version
+ if (sys.version_info[0] < 3):
+ print("TRANSIT v3.0+ requires python3.6+. To use with python2, please install TRANSIT version < 3.0")
+ sys.exit(0)
vars = Globals()
# Check for arguements
if not args and not kwargs and hasWx:
=====================================
src/pytpp/tpp_tools.py
=====================================
@@ -1442,6 +1442,7 @@ def show_help():
print(' -maxreads <INT>')
print(' -mismatches <INT> # when searching for constant regions in reads 1 and 2; default is 1')
print(' -flags "<STRING>" # args to pass to BWA')
+ print(' -bwa-alg [aln|mem] # Default: mem. Algorithm to use for mapping reads with bwa' )
print(' -primer-start-window INT,INT # position in read to search for start of primer; default is [0,20]')
print(' -window-size INT # automatic method to set window')
print(' -barseq_catalog_in|-barseq_catalog_out <file>')
=====================================
src/pytransit/__init__.py
=====================================
@@ -2,6 +2,6 @@
__all__ = ["transit_tools", "tnseq_tools", "norm_tools", "stat_tools"]
-__version__ = "v3.0.0"
+__version__ = "v3.0.1"
prefix = "[TRANSIT]"
=====================================
src/pytransit/__main__.py
=====================================
@@ -43,6 +43,10 @@ def run_main():
main(*args, **kwargs)
def main(*args, **kwargs):
+ # Check python version
+ if (sys.version_info[0] < 3):
+ print("TRANSIT v3.0+ requires python3.6+. To use with python2, please install TRANSIT version < 3.0")
+ sys.exit(0)
#If no arguments, show GUI:
DEBUG = "--debug" in sys.argv
if DEBUG:
=====================================
src/pytransit/analysis/gi.py
=====================================
@@ -40,10 +40,10 @@ long_name = "Genetic Interactions"
short_desc = "Genetic interactions analysis for change in enrichment"
long_desc = """Method for determining genetic interactions based on changes in enrichment (i.e. delta log fold-change in mean read counts).
-NOTE: This method requires 4 groups of datasets. Use the main interface to add datasets for the two strain backgrounds under the first condition. A window will allow you to add the datasets under the second condition.
+NOTE: This method requires 4 groups of datasets. Use the main interface to add datasets for the two strain backgrounds under the first condition. After pressing "Run GI", a subsequent window will allow you to add the datasets under the second condition.
"""
-transposons = []
+transposons = ["himar1"]
columns = ["Orf","Name","Number of TA Sites","Mean count (Strain A Condition 1)","Mean count (Strain A Condition 2)","Mean count (Strain B Condition 1)","Mean count (Strain B Condition 2)", "Mean logFC (Strain A)", "Mean logFC (Strain B)", "Mean delta logFC","Lower Bound delta logFC","Upper Bound delta logFC", "Prob. of delta-logFC being within ROPE", "Adjusted Probability (BFDR)", "Is HDI outside ROPE?", "Type of Interaction"]
=====================================
src/pytransit/analysis/multitnseq.py deleted
=====================================
@@ -1,572 +0,0 @@
-import sys
-import os
-import io
-
-hasR = False
-try:
- import rpy2.robjects
- hasR = True
-except Exception as e:
- hasR = False
-
-import base
-import numpy
-import scipy
-import pdfkit
-import statsmodels.stats.multitest
-import statsmodels.stats.multicomp
-import pytransit.transit_tools as transit_tools
-import pytransit.tnseq_tools as tnseq_tools
-import pytransit.norm_tools as norm_tools
-from multitnseq_helpers import def_r_samples_corrplot, def_r_clustering, def_r_make_heatmap, def_r_conditions_corrplot
-
-###### GUI ELEMENTS ######
-short_name = "MultiTnSeq"
-long_name = "MultiTnSeq"
-short_desc = "Run the MultiTnSeq pipeline"
-long_desc = """Run the MultiTnSeq pipeline"""
-transposons = ["", ""]
-EOL = "\n"
-
-class MultiTnSeqAnalysis(base.TransitAnalysis):
- def __init__(self):
- base.TransitAnalysis.__init__(self, short_name, long_name, short_desc, long_desc, transposons, MultiTnSeqMethod)
-
-class MultiTnSeqMethod(base.AnalysisMethod):
- """
- MultiTnSeq pipeline, uses R scripts
- """
- def __init__(self, fna, annotation, combined_wig, metadata, cond_metadata, output_file, K, D, debatch, stdnorm):
- base.AnalysisMethod.__init__(self, short_name, long_name, short_desc, long_desc, output_file, annotation)
- self.ref = fna
- self.annotation = annotation
- self.combined_wig = combined_wig
- self.samples_metadata_fname = metadata
- self.conditions_metadata_fname = cond_metadata
- self.output_file = output_file
- self.K = K
- self.D = D
- self.debatch = False
- self.stdnorm = False
- self.rundir = ""
-
- @classmethod
- def fromargs(self, rawargs):
- if not hasR:
- print("Error: R and rpy2 (< 2.9.0) required to run ZINB analysis.")
- print("After installing R, you can install rpy2 using the command \"pip install 'rpy2<2.9.0'\"")
- sys.exit(0)
-
- (args, kwargs) = transit_tools.cleanargs(rawargs)
-
- if (kwargs.get('-help', False) or kwargs.get('h', False)):
- print(MultiTnSeqMethod.usage_string())
- sys.exit(0)
-
- fna = args[0]
- annotation = args[1]
- combined_wig = args[2]
- metadata = args[3]
- cond_metadata = args[4]
- output_file = args[5]
- K = kwargs.get("K", 10)
- D = kwargs.get("D", 5)
- debatch = kwargs.get("-debatch", False)
- stdnorm = kwargs.get("-stdnorm", False)
-
- return self(fna, annotation, combined_wig, metadata, cond_metadata, output_file, K, D, debatch, stdnorm)
-
- def read_genes(self, fname, descriptions=False):
- genes = []
- for line in open(fname):
- w = line.split('\t')
- data = [int(w[1])-1,int(w[2])-1,w[8],w[7],w[3]]
- if descriptions==True: data.append(w[0])
- genes.append(data)
- return genes
-
- def read_genome(self, filename):
- s = ""
- n = 0
- for line in open(filename):
- if n==0: n = 1 # skip first
- else: s += line[:-1]
- return s
-
- def hash_genes(self, genes,genome):
- hash = {}
- for gene in genes:
- a,b = gene[0],gene[1]
- for i in range(a,b+1):
- hash[i] = gene
- return hash
-
- def makefname(self, name,dir):
- if dir=="": return name
- else: return "%s/%s" % (dir,name)
-
- def Run(self):
- print("Running")
- # self.generate_pdf()
- # self.transit_message("Done.")
-
- Samples = tnseq_tools.Spreadsheet(self.makefname(self.samples_metadata_fname, self.rundir))
- Conditions = tnseq_tools.Spreadsheet(self.makefname(self.conditions_metadata_fname, self.rundir))
-
- genome = self.read_genome(self.makefname(self.ref,self.rundir))
- genes = self.read_genes(self.makefname(self.annotation,self.rundir))
- ghash = self.hash_genes(genes,genome)
-
- datasets = Samples.getcol("Filename") # filenames
-
- (sites, data, filenamesInCombWig) = tnseq_tools.read_combined_wig(self.makefname(self.combined_wig, self.rundir)) # data: rows are TA sites, cols are datasets
- # "datasets" are columns (indexes) in combined wig (data)
- # SampleIndexes are list of rows in Samples to be analyzed (contains Filenames and Conditions), i.e. which datasets (row indexes in data) represent each condition?
- # wigindexes are corresponding columns in data (from original order, matched by Filename)
-
- SampleIndexes,wigindexes = [],[]
- for cond in Conditions.keys:
- for row in range(Samples.nrows):
- if Samples.get(row,"Condition") == cond:
- fname = Samples.get(row,"Filename")
- if fname not in filenamesInCombWig:
- print "error: filename '%s' listed in samples metadata not found in combined wig file" % fname; sys.exit(0)
- SampleIndexes.append(row)
- wigindexes.append(filenamesInCombWig.index(fname))
-
- # reordering data matrix (select columns, order by cond) for normalization; now should be parallel to SampleIndexes
- data = data[wigindexes, :]
- data = data[wigindexes, :]
- neworder = [filenamesInCombWig[i] for i in wigindexes]
- filenamesInData = neworder
-
- # foreach cond, list of indexes into data
- cond2datasets = {}
- for cond in Conditions.keys:
- cond2datasets[cond] = []
- for row in range(Samples.nrows):
- if Samples.get(row,"Condition")==cond:
- fname = Samples.get(row,"Filename")
- cond2datasets[cond].append(filenamesInData.index(fname))
- if len(cond2datasets[cond]) == 0:
- print "error: no samples found in metadata for condition %s" % cond; sys.exit(0)
-
- (normed, factors) = norm_tools.normalize_data(data, method='TTR')
- Nds,Nsites = normed.shape # transposed: rows are datasets, cols are TA sites
-
- file = open(self.makefname("temp_counts_TTR.txt", self.rundir),"w")
- vals = "coord ORF gene".split()+[Samples.get(r,"Id") for r in SampleIndexes] # in order of Conditions
- file.write('\t'.join(vals)+EOL)
- for i,co in enumerate(sites):
- rv,gene = "igr","igr"
- if co in ghash:
- annot = ghash[co]
- rv,gene = annot[2],annot[3]
- vals = [str(co),rv,gene]+["%0.1f" % (int(x)) for x in list(normed[:,i])]
- file.write('\t'.join([str(x) for x in vals])+EOL)
- file.close()
-
- r_correlation = def_r_samples_corrplot()
- r_correlation("temp_counts_TTR.txt")
-
- # write table of stats (saturation,NZmean)
- file = open(self.makefname("temp_stats.txt", self.rundir),"w")
- file.write("dataset\tdensity\tmean_ct\tNZmean\tNZmedian\tmax_ct\ttotal_cts\tskewness\tkurtosis\n")
- for i in range(data.shape[0]):
- density, meanrd, nzmeanrd, nzmedianrd, maxrd, totalrd, skew, kurtosis = tnseq_tools.get_data_stats(data[i,:])
- vals = [filenamesInData[i], "%0.2f" % density, "%0.1f" % meanrd, "%0.1f" % nzmeanrd, "%d" % nzmedianrd, maxrd, totalrd, "%0.1f" % skew, "%0.1f" % kurtosis]
- file.write('\t'.join([str(x) for x in vals])+EOL)
- file.close()
-
- ################################
-
- # new version, hashes on Rv
-
- siteshash = {}
- for i,TA in enumerate(sites): siteshash[TA] = i
-
- TAsites = {}
- for g,(start,end,Rv,gene,strand) in enumerate(genes):
- siteindexes = []
- for i in range(start,end): # end+1?
- co = i+1
- if co in siteshash: siteindexes.append(siteshash[co])
- TAsites[Rv] = siteindexes
-
-
-
- if False: # print means for each gene for each dataset
- print '\t'.join(filenamesInData)
- print '\t'.join([Samples.get(x,"Id") for x in SampleIndexes])
- for (start,end,Rv,gene,strand) in genes:
- if len(TAsites[Rv])>0: # skip genes with no TA sites
- means = []
- for j in range(Nds):
- obs = normed[j,TAsites[Rv]]
- means.append(numpy.mean(obs))
- print '\t'.join([Rv,gene,str(len(TAsites[Rv]))]+["%0.1f" % x for x in means])
- #sys.exit(0)
-
-
- Counts = {} # sub-arrays of (datasets X sites) for genes X conds, where #TAs>0
- for (start,end,Rv,gene,strand) in genes:
- siteindexes = TAsites[Rv]
- local = normed[:,siteindexes]
- counts = []
- for j in range(Conditions.nrows):
- cond = Conditions.get(j,"Condition")
- obs = local[cond2datasets[cond],:]
- counts.append(obs) # sub-matrices
- Counts[Rv] = counts
-
- Means = {}
- for (start,end,Rv,gene,strand) in genes:
- if len(TAsites[Rv])>0: # skip genes with no TA sites
- means = []
- for j in range(Conditions.nrows):
- cond = Conditions.get(j,"Condition")
- obs = Counts[Rv][j]
- means.append(numpy.mean(obs))
- Means[Rv] = means
-
- file = open(self.makefname("temp_gene_means.txt", self.rundir),"w")
- file.write('\t'.join("ORF Gene TAs".split()+Conditions.getcol('Condition'))+EOL)
- for (start,end,Rv,gene,strand) in genes:
- if Rv not in Means: continue # skip genes with no TA sites
- means,sites = Means[Rv],TAsites[Rv]
- file.write('\t'.join([Rv,gene,str(len(sites))]+["%0.1f" % x for x in means])+EOL)
- file.close()
-
- ################################
- # do ANOVA to identify genes with significant variability
- # it is much faster to do this in python than R (and don't have to create the melted file)
-
- pvals,Rvs, = [],[] # lists
- for (start,end,Rv,gene,strand) in genes:
- if Rv in Means:
- countsvec = Counts[Rv]
- countsvec = [x.flatten() for x in countsvec]
- stat,pval = scipy.stats.f_oneway(*countsvec)
- pvals.append(pval)
- Rvs.append(Rv)
-
- pvals = numpy.array(pvals)
- mask = numpy.isfinite(pvals)
- qvals = numpy.full(pvals.shape,numpy.nan)
- qvals[mask] = statsmodels.stats.multitest.fdrcorrection(pvals[mask])[1] # BH, alpha=0.05
-
- p,q = {},{}
- for i,rv in enumerate(Rvs):
- p[rv],q[rv] = pvals[i],qvals[i]
- pvals,qvals = p,q, # hashes on Rv
-
- # post-hoc analysis to identify "high" and "low" subgroups
- Sortedmeans,Divisions = {},{} # sortedmeans: list of (mean,cond); divisions: list of (lowsubset,highsubset) or None
- for (start,end,Rv,gene,strand) in genes:
- if Rv in qvals and qvals[Rv]<0.05:
- #print Rv,gene
- countsvec = Counts[Rv]
- countsvec = [x.flatten() for x in countsvec]
- allcounts,allconds = numpy.array([]),numpy.array([])
- for j in range(len(Conditions.keys)):
- allcounts = numpy.append(allcounts,countsvec[j])
- for k in range(len(countsvec[j])):
- allconds = numpy.append(allconds,Conditions.keys[j])
- mc = statsmodels.stats.multicomp.MultiComparison(allcounts,allconds)
- tuk = mc.tukeyhsd() # alpha=0.1
- #print tuk
- reject,n = {},0
- groups = tuk.groupsunique.tolist()
- for j,group1 in enumerate(groups):
- for k,group2 in enumerate(groups):
- if j<k: reject[(group1,group2)] = reject[(group2,group1)] = tuk.reject[n]; n += 1
- sortedmeans = [(numpy.mean(countsvec[k]),Conditions.keys[k]) for k in range(len(countsvec))] # list of (mean,condname)
- sortedmeans = sorted(sortedmeans)
- Sortedmeans[Rv] = sortedmeans
- sortedgroups = [x[1] for x in sortedmeans]
- #for (m,c) in sortedmeans: print c,"%0.1f" % m
- candidate_divisions = [] # lists of condition names in 2 subgroups (lower and higher, but not necessarily in that order)
- for j in range(1,len(sortedmeans)):
- lowsubset,highsubset = sortedgroups[:j],sortedgroups[j:]
- alldistinct = True
- for group1 in lowsubset:
- for group2 in highsubset: alldistinct = alldistinct and reject[(group1,group2)]; # print group1,group2,reject[(group1,group2)]
- diff = sortedmeans[j][0]-sortedmeans[j-1][0] # could be negative if conds not sorted
- vals = lowsubset+['<<<--->>>']+highsubset+["%s" % alldistinct,"%0.1f" % diff]
- #print '\t'.join(vals)
- if diff<0: diff,lowsubset,highsubset = -diff,highsubset,lowsubset
- if alldistinct==True: candidate_divisions.append((diff,lowsubset,highsubset))
- if len(candidate_divisions)>0:
- candidate_divisions.sort(reverse=True)
- (diff,lowsubset,highsubset) = candidate_divisions[0]
- Divisions[Rv] = (lowsubset,highsubset)
-
- #The tukeyhsd of statsmodels doesn't return P value.
- #So, if you want to know P value, calculate from these outputted value or use R.
- #After saving the output into a variable res, you can get p-values by applying
- # psturng(np.abs(res.meandiffs / res.std_pairs), len(res.groupsunique), res.df_total), where psturng comes from from statsmodels.stats.libqsturng import psturng
-
- # save pvals as temp_anova.txt
- file = open(self.makefname("temp_anova.txt", self.rundir),"w")
- vals = "Rv Gene TAs".split()+Conditions.keys+"pval padj".split()
- file.write('\t'.join(vals)+EOL)
- for (start,end,Rv,gene,strand) in genes:
- if Rv in Means:
- m,s = numpy.mean(Means[Rv]),numpy.std(Means[Rv])
- scv = s/m
- vals = [Rv,gene,str(len(TAsites[Rv]))]+["%0.1f" % x for x in Means[Rv]]+["%f" % x for x in [pvals[Rv],qvals[Rv]]] # could append SCV, but beware of how multi_TnSeq.py counts hits in temp_anova.txt
- file.write('\t'.join(vals)+EOL)
- file.close()
-
- # write sorted means and high/low subgroups into temp_subgroups.txt
- file = open(self.makefname("temp_divisions.txt", self.rundir),"w")
- vals = "Rv Gene TAs".split()+Conditions.keys
- file.write('\t'.join(vals)+EOL)
- for (start,end,Rv,gene,strand) in genes:
- if Rv in qvals and qvals[Rv]<0.05:
- vals = [Rv,gene,str(len(TAsites[Rv]))]+["%0.1f" % x for x in Means[Rv]]
- vals += [x[1] for x in Sortedmeans[Rv]]+["%0.1f" % x[0] for x in Sortedmeans[Rv]]
- if Rv in Divisions:
- (lowsubset,highsubset) = Divisions[Rv]
- vals += [','.join(lowsubset),','.join(highsubset)]
- file.write('\t'.join(vals)+EOL)
- file.close()
-
-
- if False: # print gene means for each condition, and batch means
- for (start,end,Rv,gene,strand) in genes:
- vals = []
- if Rv in Means:
- batches = {}
- for r in range(Conditions.nrows):
- batch = Conditions.get(r,"Batch")
- if batch not in batches: batches[batch] = []
- batches[batch].append(Means[Rv][r])
- vals.append(Means[Rv][r]) ###
- for b in "CC1 CC2 CC3 KO".split(): vals.append(numpy.mean(batches[b]))
- print '\t'.join([Rv,gene]+["%0.1f" % x for x in vals]) ###
- ###sys.exit(0)
-
-
-
- # remove batch effects (subtract batch means from mean gene counts; adjust each to global mean)
- if self.debatch and "Batch" in Conditions.headers:
- print "<BR>correcting means for batch effects..."
- for (start,end,Rv,gene,strand) in genes:
- if Rv in Means:
- batches = {}
- for r in range(Conditions.nrows):
- batch = Conditions.get(r,"Batch")
- if batch not in batches: batches[batch] = []
- batches[batch].append(Means[Rv][r])
-
- globalmean = numpy.mean(Means[Rv])
- keys = sorted(batches.keys())
- batchmeans = {}
- for b in keys: batchmeans[b] = numpy.mean(batches[b])
-
- for r in range(Conditions.nrows):
- batch = Conditions.get(r,"Batch")
- delta = globalmean-batchmeans[batch] # correction for each batch
- Means[Rv][r] = max(0,Means[Rv][r]+delta)
-
- if False: # print gene means for each condition (with batch corrections)
- vals = ['ORF','gene']+Conditions.getcol("Condition")
- print '\t'.join(vals)
- for (start,end,Rv,gene,strand) in genes:
- if Rv not in Means: continue
- vals = [Means[Rv][r] for r in range(Conditions.nrows)]
- print '\t'.join([Rv,gene]+["%0.1f" % x for x in vals])
- sys.exit(0)
-
- ################################
- # calc LFCs
-
- # consider normalizing by reference conditions?
- # consider only calculating for non-reference conditions?
-
- lfcs = {}
- for (start,end,Rv,gene,strand) in genes:
- if Rv in qvals and qvals[Rv]<0.05:
- lfcvec = []
- for j in range(Conditions.nrows): # could remove means for reference conditions
- a = Means[Rv][j]
- b = numpy.median(Means[Rv])
- PC = 5
- lfc = numpy.log2((a+5)/float(b+5))
- lfcvec.append(lfc)
- lfcs[Rv] = lfcvec
-
- if self.stdnorm:
- print "<BR>applying standard normalization to LFCs"
- for i,cond in enumerate(Conditions.keys):
- col = [row[i] for row in lfcs.values()]
- m,s = numpy.mean(col),numpy.std(col) # consider using quantiles(col,[0,0.25,0.5,0.75,1.0])
- for Rv in lfcs.keys():
- lfcs[Rv][i] = (lfcs[Rv][i]-m)/s
-
- file = open(self.makefname("temp_LFCs.txt", self.rundir),"w")
- vals = "Rv Gene".split()+Conditions.keys # or non-ref-conds
- file.write('\t'.join(vals)+EOL)
- cnt = 0
- for (start,end,Rv,gene,strand) in genes:
- if Rv in qvals and qvals[Rv]<0.05:
- vals = [Rv,gene]+["%0.3f" % x for x in lfcs[Rv]]
- file.write('\t'.join([str(x) for x in vals])+EOL)
- cnt += 1
- file.close()
- if cnt==0: print "error: no significantly varying genes found by ANOVA"; return
-
- r_conditions_corrplot = def_r_conditions_corrplot()
- r_make_heatmap = def_r_make_heatmap()
- r_clustering = def_r_clustering()
-
- r_conditions_corrplot("temp_LFCs.txt")
- r_make_heatmap("temp_LFCs.txt")
- r_clustering("temp_LFCs.txt", self.K, self.D)
-
- self.generate_pdf()
- self.transit_message("Done.")
-
- def to_html(self):
- stats_table = '<table border="1" cellpadding="5" cellspacing="0">'
- for line in open("temp_stats.txt"):
- w = line.rstrip().split('\t')
- stats_table += "<tr>"
- for val in w:
- stats_table += "<td>" + val + "</td>"
- stats_table += "</tr>"
- stats_table += '</table>'
- lfcs_path = os.getcwd() + "/lfcs_boxplot.png"
-
- corr_plot = '<p><br>lfcs_boxplot.png:<br><img src="{0}"></p>'.format(lfcs_path)
-
- anova_varying = 0
- skip = 1
- for line in open("temp_anova.txt"):
- # skip header lines
- if skip > 0: skip -= 1; continue
- w = line.rstrip().split("\t")
- if w[-1] != 'nan' and float(w[-1]) < 0.05: anova_varying += 1
-
- anova_results = '<p>ANOVA finds {0} significantly varying genes'.format(anova_varying)
- conditions_corrplot_path = os.getcwd() + "/conditions_corrplot.png"
- conditions_corrplot = '<p><br>conditions_corrplot.png:<br><img src="{0}"></p>'.format(conditions_corrplot_path)
- lfcs_heatmap = "<p><br>heatmap.png:<BR><img src='{0}'></p>".format(os.getcwd() + "/heatmap.png")
- cluster_analysis = ''' '''
-
- return '''
- <p>
- Links
- <ul>
- <li> <a href="temp_stats.txt">spreadsheet of statistics on TnSeq datasets</a>
- <li> <a href="temp_counts_TTR.txt">spreadsheet of normalized counts</a>
- <li> <a href="temp_anova.txt">spreadsheet with gene means and Anova results</a>
- <li> <a href="temp_clust.txt">spreadsheet with LFCs and clusters</a>
- <li> <a href="temp_divisions.txt">spreadsheet with divisions of conditions into low and high subgroups for significantly varying genes </a>
- <li> <a href="temp_scores.txt"> spreadsheet with loadings of genes onto Varimax dimensions, along with normalized associations</a>
- <li> <a href="PFilteredValues.txt"> text file with enriched functional categories in each clusters</a>
- </ul>
- </p>
- <hr>
- <H3>Quality Control</H3>
- <P>Statistics of TnSeq datasets:<BR>
- {stats_table}
- {corr_plot}
- <hr>
- {anova_results}
- <br>
- Conditions corrplot is based on significantly varying genes
- {conditions_corrplot}
- <hr>
- <h3>Cluster Analysis</h3>
- <p>LFCs are relative to the median across all conditions</p>
- {lfcs_heatmap}
- '''.format(
- stats_table=stats_table,
- corr_plot=corr_plot,
- anova_results=anova_results,
- conditions_corrplot=conditions_corrplot,
- lfcs_heatmap=lfcs_heatmap
- )
-# print "<HR>"
-# print "<H3>Cluster Analysis</H3>"
-
-# print "<P>LFCs are relative to the median across all conditions"
-# newfname = "%s/heatmap.png" % dir
-# print "<BR>heatmap.png:<BR><img src='%s'>" % newfname
-
-# newfname = "%s/cluster_opt.png" % dir
-# print "<P>cluster_opt.png:<BR><img src='%s'>" % newfname
-
-# newfname = "%s/pca_genes.png" % dir
-# print "<P>LD-PCA, colored by Kmeans cluster (K=%s)" % K
-# print "<BR>pca_genes.png:<BR><img src='%s'>" % newfname
-
-# newfname = "%s/hclust_genes.png" % dir
-# print "<P>hclust_genes.png:<BR><img src='%s'>" % newfname
-
-# newfname = "%s/hclust_conditions.png" % dir
-# print "<P>hclust_conditions.png:<BR><img src='%s'>" % newfname
-
-
-# print "<HR>"
-
-# print "<H3>Pathway Enrichment</H3>"
-
-# print """This analysis shows which functional categories are enriched in each cluster.
-# It uses the Sanger annotation (based on Cole's original descriptions of ORF functions,
-# with updates. Only the categories with <I>adjusted p-values</I> < 0.05 are shown below.
-# P-values were calculated using the Hypergeometric distribution, and
-# the multiple-test correction by the Benjamini-Hochberg procedure
-# was applied to control the FDR at 5%."""
-
-# from functionPathWay import sangerClassification
-# sangerRoles="H37Rv.sanger_roles2"
-# protTable="%s/ref.prot_table" % dir
-# clusters="%s/temp_clust.txt" %dir
-# resultFileName="%s/PFilteredValues.txt" % dir
-# sangerClassification(sangerRoles,protTable,clusters,resultFileName)
-
-# print "<PRE>"
-# for line in open(resultFileName):
-# print line,
-# print "</PRE>"
-
-# print "<HR>"
-
-# print "<H3>Principle Component Analysis</H3>"
-
-
-# print "<P>Mapping of activators onto Principle Components"
-# newfname = "%s/pca_conditions.png" % dir
-# print "<BR>pca_conditions.png:<BR><img src='%s'>" % newfname
-
-# newfname = "%s/condition_PCs.png" % dir
-# print "<P>condition_PCs.png:<BR><img src='%s'>" % newfname
-
-# newfname = "%s/varimax.png" % dir
-# print "<P>varimax.png:<BR><img src='%s'>" % newfname
-# print "</BODY></HTML>"
-
- def generate_pdf(self):
- html_content = self.to_html()
- file_name = os.path.splitext(os.path.basename(self.output_file))[0]
- with open("{0}.html".format(file_name), 'w') as f:
- f.write(html_content)
- pdfkit.from_string(html_content, "{0}.pdf".format(file_name))
-
- @classmethod
- def usage_string(self):
- return """
- python %s multitnseq <ref.fna> <ref.prot_table> <combined_wig> <samples_metadata> <conditions_metadata> <output_filename> [-K n] [-D n] [-debatch] [-stdnorm]
- """ % (sys.argv[0])
-
-def main():
- print("MultiTnseq example.")
-
- return self()
-
-if __name__ == "__main__":
- main()
-
=====================================
src/pytransit/analysis/multitnseq_helpers.py deleted
=====================================
@@ -1,203 +0,0 @@
-from rpy2.robjects import r, globalenv
-
-def def_r_clustering():
- r('''
- r_clustering = function(data_filename, K, D) {
- # input: temp_LFCs.txt
- data = read.table(data_filename,head=T,sep='\t')
- lfcs = data[,3:length(colnames(data))]
- labels = paste(data$Rv,'/',data$Gene,sep="")
- rownames(lfcs) = labels
-
- R = length(rownames(lfcs)) # genes
- C = length(colnames(lfcs)) # conditions
-
- library(corrplot)
-
- fname = "lfcs_boxplot.png"
- png(fname,width=300+15*C,height=500)
- boxplot(lfcs,las=2,ylab="log2 fold change of genes (relative to the median)")
- dev.off()
-
- km = kmeans(lfcs,K)
- clusters = km$cluster
-
- write.table(data.frame(lfcs,clust=clusters),"temp_clust.txt", sep='\t', quote=F)
-
- pca = prcomp(t(lfcs))
-
- library(MASS)
- mat = as.matrix(lfcs)
- ldapca = lda(clusters~.,lfcs)
- X = mat %*% ldapca$scaling[,1]
- Y = mat %*% ldapca$scaling[,2]
- fname = "pca_genes.png"
- png(fname,width=1000,height=1000)
- plot(X,Y,pch=20)
- text(X,Y,label=labels,adj=c(0.5,1.5),col=clusters)
- dev.off()
-
- actpca = prcomp(lfcs,center=TRUE,scale=TRUE)
- fname = "pca_conditions.png"
- png(fname,width=500,height=500)
- plot(actpca$rotation[,1:2],pch=20)#,xlim=c(-1,1),ylim=c(-1,1))
- text(actpca$rotation[,1:2],label=colnames(lfcs),adj=c(0.5,1.5),cex.lab=1.5)
- dev.off()
-
- print(length(lfcs[,1]))
- hc = hclust(dist(lfcs),method="ward.D2")
- print("****hclust_genes****")
- print(hc)
- fname = "hclust_genes.png"
- png(fname,width=300+15*R,height=600)
- plot(hc)
- K2 = max(2,min(K,max(hc$height)))
- rect.hclust(hc,k=K2,border='red')
- dev.off()
-
- hc = hclust(dist(t(lfcs)),method="ward.D2")
- print("****hclust_conditions****")
- print(hc)
- fname = "hclust_conditions.png"
- png(fname,width=300+15*C,height=600)
- # plot(hc)
- # D2 = max(2,min(D,C-1))
- # rect.hclust(hc,k=D2,border='red')
- # dev.off()
-
- fname = "cluster_opt.png"
- png(fname)
- library(factoextra)
- fviz_nbclust(lfcs, kmeans, method = "wss",k.max=30) # or silhouette or gap_stat
- #fviz_nbclust ( lfcs, kmeans, method = "wss",k.max=30)+geom_hline ( yintercept=52 )+geom_vline(xintercept=10)
- dev.off()
-
- ####################################################
- # required factoextra and corrplot libraries
-
- var = get_pca_var(actpca)
- fname = "condition_PCs.png"
- png(fname,width=1000,height=1000)
- corrplot(var$cor,main="Principle Components",mar=c(1,1,1,1))
- dev.off()
-
- S = diag(actpca$sdev,D,D)
- rawLoadings = actpca$rotation[,1:D] %*% S
- vmax = varimax(rawLoadings)
- rotatedLoadings = vmax$loadings
- rotatedScores = scale(actpca$x[,1:D]) %*% vmax$rotmat
-
- # https://stats.stackexchange.com/questions/59213/how-to-compute-varimax-rotated-principal-components-in-r
- # scores = U.S = X.V = actpca$x = scale(lfcs) %*% actpca$rotation
- combined_transform = (actpca$rotation[,1:D] %*% S) %*% vmax$rotmat
- # vmax$loadings is same as combined_transform, but with abs(vals)<0.1 blanked out
- write.table(round(combined_transform,6),"varimax_loadings.txt",sep='\t',quote=F)
-
- fname = "varimax.png"
- png(fname,width=800,height=800)
- corrplot(rotatedLoadings,main="Varimax loadings",mar=c(1,1,1,1))
- dev.off()
-
- scores = rotatedScores
- colnames(scores) = paste("score",seq(1:D),sep="")
- squares = scores*scores
- ss = apply(squares,1,sum)
- cos2 = squares/ss
- best = as.matrix(apply(cos2,1,max))
- assoc = cos2*sign(scores)
- colnames(assoc) = paste("assoc",seq(1:D),sep="")
-
- # # generate null distribution for cos2 to closest axis
- #
- # library(MASS)
- # SAMPLES = 10000
- # sample = mvrnorm(n=SAMPLES,mu=rep(0,D),Sigma=diag(D))
- # # no need to apply Varimax rotation
- # squares = sample*sample
- # ss = apply(squares,1,sum)
- # Xcos2 = squares/ss
- # Xbest = as.matrix(apply(Xcos2,1,max))
- # #distn = ecdf(best)
- # pvals = apply(best,1,function (x) { length(Xbest[Xbest>=x]) })
- # pvals = pvals/SAMPLES
- # padj = p.adjust(pvals,method="BH")
-
- #res = data.frame(data,scores,assoc,best,pvals,padj)
- res = data.frame(data,scores,assoc)
- write.table(format(res,digits=3,scientific=F), "temp_scores.txt",sep='\t',quote=F,row.names=F)
-
- }
- ''')
- return globalenv['r_clustering']
-
-def def_r_samples_corrplot():
- r('''
- r_samples_corrplot = function(data_filename) {
- data = read.table(data_filename, sep='\t',head=T)
- vals = as.matrix(data[,4:length(colnames(data))])
- N = length(colnames(vals))
-
- library(corrplot)
-
- fname = "samples_corrplot.png"
- png(fname,width=300+20*N,height=300+20*N)
- #corrplot(cor(vals)) # among TAsites (not good)
-
- TAsites = aggregate ( coord~ORF,data=data,length)
- colnames(TAsites) = c("ORF","sites")
- temp = aggregate(vals,by=list(data$ORF),FUN=mean)
- corrplot(cor(temp[TAsites$sites>=10,2:length(colnames(temp))]))
-
- dev.off()
- }''')
-
- return globalenv['r_samples_corrplot']
-
-def def_r_conditions_corrplot():
- r('''
- r_conditions_corrplot = function(data_filename) {
- data = read.table(data_filename, sep='\t', head=T)
- vals = as.matrix(data[,3:length(colnames(data))])
- N = length(colnames(vals))
-
- library(corrplot)
-
- png("conditions_corrplot.png", width=20*N+300, height=20*N+300)
- corrplot(cor(vals))
- dev.off()
- }
- ''')
-
- return globalenv['r_conditions_corrplot']
-
-
-def def_r_make_heatmap():
- r('''
- r_make_heatmap = function(data_filename) {
- data = read.table(data_filename, head=T, sep='\t')
- lfcs = as.matrix(data[,3:length(colnames(data))])
- labels = paste(data$Rv,'/',data$Gene,sep="")
- rownames(lfcs) = labels
-
- library(corrplot)
- library(RColorBrewer)
- library(gplots)
-
- # Red for down regulated, green for upregulated.
- redgreen <- function(n) { c( hsv(h=0/6, v=seq(1,0,length=n/2) ), hsv(h=2/6, v=seq(0,1,length=n/2) ), ) }
- colors <- colorRampPalette(c("red", "white", "green"))(n = 1000)
-
- C = length(colnames(lfcs))
- R = length(rownames(lfcs))
- W = 300+C*30
- H = 300+R*15
-
- fname = "heatmap.png"
- png(fname,width=W,height=H)
- #par(oma=c(10,1,1,10)) # b,l,t,r; units="lines of space"
- heatmap.2(lfcs,col=colors,margin=c(12,12),lwid=c(1,7),lhei=c(1,7),trace="none",cexCol=1.4,cexRow=1.4) # make sure white=0
- dev.off()
- }
- ''')
- return globalenv['r_make_heatmap']
-
=====================================
src/pytransit/analysis/pathway_enrichment.py
=====================================
@@ -177,13 +177,13 @@ class GSEAMethod(base.SingleConditionMethod):
n = len(dict_n[key])
I = set(dict_k) & set(dict_n[key])
k = len(I)
- result[key] = {"parameters":str(k)+"\t"+str(n),"p-value": hypergeom.sf(k,M,n,N), "Intersection":I}
+ result[key] = {"parameters":str(n)+"\t"+str(k),"p-value": hypergeom.sf(k,M,n,N), "Intersection":I}
self.padjustForHypergeom(result)
return result
def padjustForHypergeom(self,result):
- keys = result.keys()
+ keys = list(result.keys())
pvalues = [result[k]["p-value"] for k in keys]
b,adj=multitest.fdrcorrection(pvalues, alpha=0.05, method='indep')
for i in range(len(keys)):
@@ -357,7 +357,7 @@ class GSEAMethod(base.SingleConditionMethod):
self.output.close()
def padjustTest(self,test):
- keys = test.keys()
+ keys = list(test.keys())
pvals = [test[k][2] for k in keys]
b,adj=multitest.fdrcorrection(pvals, alpha=0.05, method='indep')
for i in range(len(keys)):
@@ -453,7 +453,7 @@ class GSEAMethod(base.SingleConditionMethod):
self.output.write("#%s\n" % "\t".join(columns))
self.saveExit(gseaVal,PathDict,rank,ORFNameDict,DESCR)
elif self.M =="HYPE":
- columns=["cat id descr","Total genes","Total in intersection","pval","padj","genes in intersection"]
+ columns=["cat id", "descr","Total genes","Total in intersection","pval","padj","genes in intersection"]
self.output.write("#%s\n" % "\t".join(columns))
self.saveHyperGeometricTest(results,ORFNameDict,DESCR)
elif self.M =="GSEA-Z":
View it on GitLab: https://salsa.debian.org/med-team/tnseq-transit/compare/435840ca66cbfb44434b26dde53146d1f8e02464...dbc03cfeb110a628731b42a14471de5e589fd2f9
--
View it on GitLab: https://salsa.debian.org/med-team/tnseq-transit/compare/435840ca66cbfb44434b26dde53146d1f8e02464...dbc03cfeb110a628731b42a14471de5e589fd2f9
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