[med-svn] [Git][med-team/cyvcf2][upstream] New upstream version 0.30.14

Nilesh Patra (@nilesh) gitlab at salsa.debian.org
Sat Dec 18 08:31:28 GMT 2021



Nilesh Patra pushed to branch upstream at Debian Med / cyvcf2


Commits:
c6bc65e7 by Nilesh Patra at 2021-12-18T13:34:36+05:30
New upstream version 0.30.14
- - - - -


17 changed files:

- .github/workflows/build.yml
- .github/workflows/wheels.yml
- CHANGES.md
- README.md
- ci/linux-deps
- ci/osx-deps
- cyvcf2/__init__.py
- cyvcf2/cyvcf2.pxd
- cyvcf2/cyvcf2.pyx
- cyvcf2/helpers.c
- cyvcf2/helpers.h
- + cyvcf2/tests/test-genotypes.vcf
- cyvcf2/tests/test_hemi.py
- cyvcf2/tests/test_reader.py
- docs/source/index.rst
- setup.cfg
- setup.py


Changes:

=====================================
.github/workflows/build.yml
=====================================
@@ -8,7 +8,7 @@ jobs:
     runs-on: ubuntu-18.04
     strategy:
       matrix:
-        python-version: [3.6, 3.7, 3.8, 3.9]
+        python-version: [3.6, 3.7, 3.8, 3.9, "3.10"]
 
     steps:
     - uses: actions/checkout at v2
@@ -23,14 +23,14 @@ jobs:
         sudo apt-get update
         sudo apt-get install libcurl4-openssl-dev
         pip install -r requirements.txt
-        pip install nose
+        pip install pytest pytest-cov
         cd htslib
         autoheader && autoconf
         ./configure --enable-s3 --disable-lzma --disable-bz2
         make
         cd ..
-        CYTHONIZE=1 python setup.py install
+        CYTHONIZE=1 python setup.py build_ext -i
     - name: Test
       run: |
-        python setup.py test
+        pytest --cov cyvcf2 --cov-report term-missing
 


=====================================
.github/workflows/wheels.yml
=====================================
@@ -32,29 +32,36 @@ jobs:
 
     - name: Install cibuildwheel
       run: |
-        python -m pip install cibuildwheel
+        python -m pip install -U cibuildwheel
 
     - name: Build wheels for Linux
       if: matrix.os == 'ubuntu-18.04'
       run: |
         python -m cibuildwheel --output-dir wheelhouse
       env:
-        CIBW_SKIP: "pp* cp27-* cp34-* cp35-* *i686*"
+        CIBW_SKIP: "pp* *i686* *musllinux*"
         CIBW_MANYLINUX_X86_64_IMAGE: manylinux2014
         CIBW_BEFORE_BUILD_LINUX: "{project}/ci/linux-deps"
         CIBW_TEST_COMMAND: "{project}/ci/test"
-        CIBW_ENVIRONMENT: "CYTHONIZE=1 LDFLAGS='-L/usr/lib64/openssl11' CPPFLAGS='-I/usr/include/openssl11' C_INCLUDE_PATH='/root/include' LIBRARY_PATH='/root/lib'"
+        CIBW_ENVIRONMENT: "CYTHONIZE=1 LIBDEFLATE=1 LDFLAGS='-L/usr/lib64/openssl11' CPPFLAGS='-I/usr/include/openssl11' C_INCLUDE_PATH='/root/include' LIBRARY_PATH='/root/lib'"
+        CIBW_REPAIR_WHEEL_COMMAND_LINUX: LD_LIBRARY_PATH='/root/lib' auditwheel repair -w {dest_dir} {wheel}
 
     - name: Build wheels for Mac OS
       if: matrix.os == 'macos-latest'
       run: |
         python -m cibuildwheel --output-dir wheelhouse
       env:
-        CIBW_SKIP: "pp* cp27-* cp34-* cp35-* *i686*"
+        CIBW_SKIP: "pp* cp310-* *i686*"
+        CIBW_ARCHS_MACOS: "x86_64 arm64"
         CIBW_MANYLINUX_X86_64_IMAGE: manylinux2014
         CIBW_BEFORE_BUILD_MACOS: "{project}/ci/osx-deps"
         CIBW_TEST_COMMAND: "{project}/ci/test"
-        CIBW_ENVIRONMENT: "CYTHONIZE=1"
+        CIBW_TEST_SKIP: "*-macosx_arm64"
+        CIBW_ENVIRONMENT: "CYTHONIZE=1 LIBDEFLATE=1 C_INCLUDE_PATH='/usr/local/include' LIBRARY_PATH='/usr/local/lib'"
+        # https://cibuildwheel.readthedocs.io/en/stable/faq/#macos-passing-dyld_library_path-to-delocate
+        CIBW_REPAIR_WHEEL_COMMAND_MACOS: >
+          DYLD_LIBRARY_PATH=/usr/local/lib delocate-listdeps {wheel} &&
+          DYLD_LIBRARY_PATH=/usr/local/lib delocate-wheel --require-archs {delocate_archs} -w {dest_dir} {wheel}
         LDFLAGS: "-L/usr/local/opt/openssl at 1.1/lib"
         CPPFLAGS: "-I/usr/local/opt/openssl at 1.1/include"
         PKG_CONFIG_PATH: "/usr/local/opt/openssl at 1.1/lib/pkgconfig"


=====================================
CHANGES.md
=====================================
@@ -1,3 +1,17 @@
+# v0.30.14
++ use warnings instead of sys.stderr (#229 from @grahamgower)
++ use libdeflate in wheel build (#231 from @grahamgower)
++ use pytest instead of nose and update numpy stuff (#232 from @grahamgower)
+
+# v0.30.13
++ fixes for mixed ploidy samples affecting `variant.num_het`,
+  `variant.num_hom_ref`, etc. Also affects `variant.genotypes` and
+  `variant.genotype` (see #227. Thanks @davmlaw and  @grahamgower for
+  test-cases and insight.)
+
+# v0.30.12
++ add variant.FILTERS (by @tomwhite, #149)
+
 # v0.30.11
 + bump for CI
 


=====================================
README.md
=====================================
@@ -107,10 +107,10 @@ For pkg-config to find openssl you may need to set:
 Testing
 =======
 
-Tests can be run with:
+Install `pytest`, then tests can be run with:
 
 ```
-python setup.py test
+pytest
 ```
 
 CLI


=====================================
ci/linux-deps
=====================================
@@ -29,6 +29,13 @@ make install
 cd ..
 rm -rf curl-7.73.0
 
+curl -L -o libdeflate-v1.8.tar.gz https://github.com/ebiggers/libdeflate/archive/refs/tags/v1.8.tar.gz
+tar xzf libdeflate-v1.8.tar.gz
+cd libdeflate-1.8
+make
+make install PREFIX=/root
+cd ..
+
 cd htslib
 # configure fails with autoconf 2.71 (in /usr/local/bin), so use 2.69 (in /usr/bin)
 /usr/bin/autoconf -V


=====================================
ci/osx-deps
=====================================
@@ -13,6 +13,13 @@ brew install autoconf at 2.69 && \
 brew link --overwrite autoconf at 2.69 && \
 autoconf -V
 
+curl -L -o libdeflate-v1.8.tar.gz https://github.com/ebiggers/libdeflate/archive/refs/tags/v1.8.tar.gz
+tar xzf libdeflate-v1.8.tar.gz
+cd libdeflate-1.8
+make
+make install
+cd ..
+
 cd htslib
 autoheader
 autoconf


=====================================
cyvcf2/__init__.py
=====================================
@@ -2,4 +2,4 @@ from .cyvcf2 import (VCF, Variant, Writer, r_ as r_unphased, par_relatedness,
                      par_het)
 Reader = VCFReader = VCF
 
-__version__ = "0.30.11"
+__version__ = "0.30.14"


=====================================
cyvcf2/cyvcf2.pxd
=====================================
@@ -13,8 +13,7 @@ cdef extern from "relatedness.h":
             int32_t n_samples, double *ab)
 
 cdef extern from "helpers.h":
-    int as_gts(int32_t *gts, int num_samples, int ploidy, int strict_gt);
-    int as_gts012(int32_t *gts, int num_samples, int ploidy, int strict_gt);
+    int as_gts(int32_t *gts, int num_samples, int ploidy, int strict_gt, int HOM_ALT, int UNKNOWN);
     int32_t* bcf_hdr_seqlen(const bcf_hdr_t *hdr, int32_t *nseq)
 
 cdef extern from "htslib/kstring.h":


=====================================
cyvcf2/cyvcf2.pyx
=====================================
@@ -12,6 +12,7 @@ import numpy as np
 from array import array
 import math
 import ctypes
+import warnings
 try:
   from pathlib import Path
 except ImportError:
@@ -350,12 +351,12 @@ cdef class VCF(HTSFile):
 
         ret = bcf_hdr_set_samples(self.hdr, <const char *>samples, 0)
         assert ret >= 0, ("error setting samples", ret)
+        self.n_samples = bcf_hdr_nsamples(self.hdr)
         if ret != 0 and samples != "-":
             s = from_bytes(samples).split(",")
-            if ret < len(s):
-                sys.stderr.write("warning: not all requested samples found in VCF\n")
+            if self.n_samples < len(s):
+                warnings.warn("not all requested samples found in VCF")
 
-        self.n_samples = bcf_hdr_nsamples(self.hdr)
 
     def update(self, id, type, number, description):
         """Update the header with an INFO field of the given parameters.
@@ -400,7 +401,7 @@ cdef class VCF(HTSFile):
 
         itr = bcf_itr_querys(self.hidx, self.hdr, to_bytes(region))
         if itr == NULL:
-            sys.stderr.write("no intervals found for %s at %s\n" % (self.fname, region))
+            warnings.warn("no intervals found for %s at %s" % (self.fname, region))
             raise StopIteration
         try:
             while True:
@@ -409,10 +410,8 @@ cdef class VCF(HTSFile):
                 if ret < 0:
                     bcf_destroy(b)
                     break
-                if bcf_subset_format(self.hdr, b) != 0:
-                    sys.stderr.write("could not subset variant")
-                    bcf_destroy(b)
-                    break
+                ret = bcf_subset_format(self.hdr, b)
+                assert ret == 0, ("could not subset variant", self.fname, region)
                 yield newVariant(b, self)
         finally:
             if itr != NULL:
@@ -454,7 +453,7 @@ cdef class VCF(HTSFile):
             itr = tbx_itr_querys(self.idx, cregion)
 
         if itr == NULL:
-            sys.stderr.write("no intervals found for %s at %s\n" % (self.fname, region))
+            warnings.warn("no intervals found for %s at %s" % (self.fname, region))
             raise StopIteration
 
         try:
@@ -905,7 +904,7 @@ cdef class VCF(HTSFile):
             nv += 1
             if nv == n_variants:
                 break
-        sys.stderr.write("tested: %d variants out of %d\n" % (nv, nvt))
+        warnings.warn("tested: %d variants out of %d" % (nv, nvt))
         return self._relatedness_finish(ibs, n, hets)
 
     cdef dict _relatedness_finish(self,
@@ -929,7 +928,7 @@ cdef class VCF(HTSFile):
         for sj in range(ns):
             sample_j = samples[sj]
             if _hets[sj] == 0:
-                print("peddy: no hets found for sample %s\n" % sample_j, file=sys.stderr)
+                warnings.warn("peddy: no hets found for sample %s" % sample_j)
             for sk in range(sj, ns):
                 if sj == sk: continue
                 sample_k = samples[sk]
@@ -1024,9 +1023,13 @@ cdef class Genotypes(object):
         cdef int32_t v
         for j in range(self.ploidy):
             v = self._raw[i * self.ploidy + j]
-            result.append((v >> 1) - 1)
+            if v != bcf_int32_vector_end:
+                result.append((v >> 1) - 1)
         return result
 
+    def __repr__(self):
+        return str(self.array())
+
     def array(Genotypes self, int fill=-2):
         """
         array returns an int16 numpy array  of shape n_samples, (ploidy + 1).
@@ -1171,7 +1174,7 @@ cdef class Variant(object):
                         if a >= -1 and b >= -1:
                           bases[j] = d[a] + lookup[phased[j]] + d[b]
                         else:
-                          bases[j] = d[a]
+                          bases[j] = d[max(-1, a)]
                 elif n == 1:
                     bases[j] = d[self._gt_idxs[i]]
                 else:
@@ -1351,9 +1354,10 @@ cdef class Variant(object):
         if self.vcf.n_samples == 0: return None
         cdef int32_t *gts = NULL
         cdef int ndst = 0
-        if bcf_get_genotypes(self.vcf.hdr, self.b, &gts, &ndst) <= 0:
+        cdef int nret = bcf_get_genotypes(self.vcf.hdr, self.b, &gts, &ndst)
+        if nret < 0:
             raise Exception("couldn't get genotypes for variant")
-        return newGenotypes(gts, int(ndst/self.vcf.n_samples), self.vcf.n_samples)
+        return newGenotypes(gts, int(nret/self.vcf.n_samples), self.vcf.n_samples)
 
     @genotype.setter
     def genotype(self, Genotypes g):
@@ -1487,12 +1491,12 @@ cdef class Variant(object):
             if self._gt_types == NULL:
                 self._gt_phased = <int *>stdlib.malloc(sizeof(int) * self.vcf.n_samples)
                 ngts = bcf_get_genotypes(self.vcf.hdr, self.b, &self._gt_types, &ndst)
-                nper = int(ndst / self.vcf.n_samples)
+                nper = int(ngts / self.vcf.n_samples)
                 self._ploidy = nper
                 self._gt_idxs = <int *>stdlib.malloc(sizeof(int) * self.vcf.n_samples * nper)
-                if ndst == 0 or nper == 0:
+                if ngts == 0 or nper == 0:
                     return np.array([])
-                for i in range(0, ndst, nper):
+                for i in range(0, ngts, nper):
                     for k in range(i, i + nper):
                         a = self._gt_types[k]
                         if a >= 0:
@@ -1504,9 +1508,9 @@ cdef class Variant(object):
                     j += 1
 
                 if self.vcf.gts012:
-                    n = as_gts012(self._gt_types, self.vcf.n_samples, nper, self.vcf.strict_gt)
+                    n = as_gts(self._gt_types, self.vcf.n_samples, nper, self.vcf.strict_gt, 2, 3)
                 else:
-                    n = as_gts(self._gt_types, self.vcf.n_samples, nper, self.vcf.strict_gt)
+                    n = as_gts(self._gt_types, self.vcf.n_samples, nper, self.vcf.strict_gt, 3, 2)
             cdef np.npy_intp shape[1]
             shape[0] = <np.npy_intp> self.vcf.n_samples
             return np.PyArray_SimpleNewFromData(1, shape, np.NPY_INT32, self._gt_types)
@@ -1700,8 +1704,8 @@ cdef class Variant(object):
         def __get__(self):
             if self.vcf.n_samples == 0:
                 return []
-            t = np.array(self.gt_depths, np.float)
-            a = np.array(self.gt_alt_depths, np.float)
+            t = np.array(self.gt_depths, float)
+            a = np.array(self.gt_alt_depths, float)
 
             # for which samples are the alt or total depths unknown?
             tU = t < 0
@@ -1893,9 +1897,7 @@ cdef class Variant(object):
                 new_rid = bcf_hdr_id2int(self.vcf.hdr, BCF_DT_CTG, new_chrom.encode())
                 if new_rid < 0:
                     raise ValueError("Unable to add {} to CHROM".format(new_chrom))
-                sys.stderr.write(
-                    "[cyvcf2]: added new contig {} to header".format(new_chrom)
-                )
+                warnings.warn("added new contig {} to header".format(new_chrom))
             self.b.rid = new_rid
 
     property var_type:
@@ -1995,6 +1997,16 @@ cdef class Variant(object):
             if ret != 0:
                 raise Exception("not able to set filter: %s", filters)
 
+    property FILTERS:
+        """the FILTER values as a list from the VCF field.
+
+        a value '.' in the VCF will return an empty list for this property
+        """
+        def __get__(self):
+            cdef int i
+            cdef int n = self.b.d.n_flt
+            return [from_bytes(bcf_hdr_int2id(self.vcf.hdr, BCF_DT_ID, self.b.d.flt[i])) for i in range(n)]
+
     property QUAL:
         "the float value of QUAL from the VCF field."
         def __get__(self):
@@ -2246,7 +2258,8 @@ cdef inline Variant newVariant(bcf1_t *b, VCF vcf):
     v.vcf = vcf
     v.POS = v.b.pos + 1
     cdef INFO i = INFO.__new__(INFO)
-    i.b, i.hdr = b, vcf.hdr
+    i.b = b 
+    i.hdr = vcf.hdr
     v.INFO = i
     return v
 


=====================================
cyvcf2/helpers.c
=====================================
@@ -1,34 +1,37 @@
 #include <helpers.h>
 
-int as_gts(int32_t *gts, int num_samples, int ploidy, int strict_gt) {
+#define MAX(x, y) (((x) > (y)) ? (x) : (y))
+
+int as_gts(int32_t *gts, int num_samples, int ploidy, int strict_gt, int HOM_ALT, int UNKNOWN) {
     int j = 0, i, k;
-    int missing= 0;
+    int missing= 0, found=0;
     for (i = 0; i < ploidy * num_samples; i += ploidy){
-		missing = 0;
-		for (k = 0; k < ploidy; k++) {
-			if (gts[i+k] <= 1) {
-				missing += 1;
-			}
-                }
-		if (missing == ploidy) {
-			gts[j++] = 2; // unknown
-			continue;
-		} else if ( (missing != 0) && (strict_gt == 1) ) {
-			gts[j++] = 2; // unknown
-			continue;
-		}
+        missing = 0;
+    found = 0;
+        for (k = 0; k < ploidy; k++) {
+            if bcf_gt_is_missing(gts[i+k])  {
+                missing += 1;
+            }
+        }
+        if (missing == ploidy) {
+            gts[j++] = UNKNOWN; // unknown
+            continue;
+        } else if ( (missing != 0) && (strict_gt == 1) ) {
+            gts[j++] = UNKNOWN; // unknown
+            continue;
+        }
 
-		if(ploidy == 1) {
-			int a = bcf_gt_allele(gts[i]);
-			if (a == 0) {
-			   	gts[j++] = 0;
-			} else if (a == 1) {
-				gts[j++] = 3;
-			} else {
-				gts[j++] = 2;
-			}
-			continue;
-		}
+        if(ploidy == 1 || gts[i+1] == bcf_int32_vector_end) {
+            int a = bcf_gt_allele(gts[i]);
+            if (a == 0) {
+                   gts[j++] = 0;
+            } else if (a == 1) {
+                gts[j++] = HOM_ALT;
+            } else {
+                gts[j++] = UNKNOWN;
+            }
+            continue;
+        }
 
         int a = bcf_gt_allele(gts[i]);
         int b = bcf_gt_allele(gts[i+1]);
@@ -44,78 +47,21 @@ int as_gts(int32_t *gts, int num_samples, int ploidy, int strict_gt) {
             continue;
         }
         else if((a == 1) && (b == 1)) {
-            gts[j] = 3; //  HOM_ALT
+            gts[j] = HOM_ALT; //  HOM_ALT
         }
         else if((a != b)) {
             gts[j] = 1; //  HET
         }
         else if((a == b)) {
-            gts[j] = 3; //  HOM_ALT
+            gts[j] = HOM_ALT; //  HOM_ALT
         } else {
-            gts[j] = 2; // unknown
+            gts[j] = UNKNOWN; // unknown
         }
         j++;
     }
     return j;
 }
 
-int as_gts012(int32_t *gts, int num_samples, int ploidy, int strict_gt) {
-    int j = 0, i, k;
-	int missing;
-    for (i = 0; i < ploidy * num_samples; i += ploidy){
-		missing = 0;
-		for (k = 0; k < ploidy; k++) {
-			if (gts[i+k] <= 1) {
-				missing += 1;
-			}
-        }
-		if (missing == ploidy) {
-			gts[j++] = 3; // unknown
-			continue;
-		} else if ( (missing != 0) && (strict_gt == 1) ) {
-			gts[j++] = 3; // unknown
-			continue;
-		}
-
-		if(ploidy == 1) {
-			int a = bcf_gt_allele(gts[i]);
-			if (a == 0) {
-			   	gts[j++] = 0;
-			} else if (a == 1) {
-				gts[j++] = 2;
-			} else {
-				gts[j++] = 3;
-			}
-			continue;
-		}
-
-        int a = bcf_gt_allele(gts[i]);
-        int b = bcf_gt_allele(gts[i+1]);
-
-        if((a == 0) && (b == 0)) {
-            gts[j++] = 0; //  HOM_REF
-            continue;
-        }
-        if ((missing > 0) && ((a == 0)  || b == 0)) {
-            gts[j] = 0; // HOM_REF
-        }
-        else if((a == 1) && (b == 1)) {
-            gts[j] = 2; //  HOM_ALT
-        }
-        else if((a  != b)) {
-            gts[j] = 1; //  HET
-        }
-        else if ((a == b)) {
-            gts[j] = 2; //  HOM_ALT
-        } else {
-            gts[j] = 3; // unknown
-        }
-        j++;
-    }
-    return j;
-}
-
-
 KHASH_MAP_INIT_STR(vdict, bcf_idinfo_t)
 typedef khash_t(vdict) vdict_t;
 
@@ -136,9 +82,9 @@ int32_t* bcf_hdr_seqlen(const bcf_hdr_t *hdr, int32_t *nseq)
         int j;
         if (lens[tid] > 0 && sscanf(kh_val(d, k).hrec[0]->vals[lens[tid]],"%d",&j) )
             lens[tid] = j;
-	if(lens[tid] > 0){
-	  found++;
-	}
+    if(lens[tid] > 0){
+      found++;
+    }
     }
     *nseq = m;
     // found is used to check that we actually got the lengths.


=====================================
cyvcf2/helpers.h
=====================================
@@ -1,6 +1,5 @@
 #include <htslib/vcf.h>
 #include <htslib/khash.h>
 
-int as_gts(int *gts, int num_samples, int ploidy, int strict_gt);
-int as_gts012(int *gts, int num_samples, int ploidy, int strict_gt);
+int as_gts(int *gts, int num_samples, int ploidy, int strict_gt, int HOM_ALT, int UNKNOWN);
 int32_t* bcf_hdr_seqlen(const bcf_hdr_t *hdr, int32_t *nseq);


=====================================
cyvcf2/tests/test-genotypes.vcf
=====================================
@@ -0,0 +1,10 @@
+##fileformat=VCFv4.1
+##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
+##FORMAT=<ID=PL,Number=G,Type=Integer,Description="Normalized, Phred-scaled likelihoods for genotypes as defined in the VCF specification">
+##contig=<ID=1,length=249250621,assembly=b37>
+#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	samplea	sampleb
+1	8466747	.	A	C	.	PASS	.	GT:PL	.:.	1:36,0
+1	8466747	.	A	C	.	PASS	.	GT:PL	./.:.	./1:36,0,40
+1	8466747	.	A	T	.	PASS	.	GT:PL	./.:.	1:36,0
+1	8466747	.	A	T	.	PASS	.	GT	0/1	0
+1	8466747	.	A	T	.	PASS	.	GT	0	0/1


=====================================
cyvcf2/tests/test_hemi.py
=====================================
@@ -1,7 +1,6 @@
 import numpy as np
 from cyvcf2 import VCF, Variant, Writer
 import os.path
-from nose.tools import assert_raises
 
 HERE = os.path.dirname(__file__)
 HEM_PATH = os.path.join(HERE, "test-hemi.vcf")


=====================================
cyvcf2/tests/test_reader.py
=====================================
@@ -1,8 +1,5 @@
 from __future__ import print_function
-from ..cyvcf2 import VCF, Variant, Writer
-import numpy as np
 import os.path
-from nose.tools import assert_raises
 import tempfile
 import sys
 import os
@@ -11,6 +8,12 @@ try:
   from pathlib import Path
 except ImportError:
   from pathlib2 import Path  # python 2 backport
+import warnings
+
+import numpy as np
+import pytest
+
+from ..cyvcf2 import VCF, Variant, Writer
 
 
 HERE = os.path.dirname(__file__)
@@ -87,11 +90,17 @@ def test_format_str():
 
 def test_missing_samples():
     samples = ['101976-101976', 'sample_not_in_vcf']
-    vcf = VCF(VCF_PATH, gts012=True, samples=samples)
+    with warnings.catch_warnings(record=True) as w:
+        vcf = VCF(VCF_PATH, gts012=True, samples=samples)
+        assert len(w) == 1
+        assert "not all requested samples found" in str(w[-1].message)
     assert len(vcf.samples) == 1
     vcf.close()
     samples = '101976-101976,sample_not_in_vcf'
-    vcf = VCF(VCF_PATH, gts012=True, samples=samples)
+    with warnings.catch_warnings(record=True) as w:
+        vcf = VCF(VCF_PATH, gts012=True, samples=samples)
+        assert len(w) == 1
+        assert "not all requested samples found" in str(w[-1].message)
     assert len(vcf.samples) == 1
 
 def test_ibd():
@@ -104,7 +113,11 @@ def test_ibd():
 
 def test_relatedness():
     vcf = VCF(VCF_PATH, gts012=True)
-    df = vcf.relatedness(gap=0, linkage_max=2)
+    with warnings.catch_warnings(record=True) as w:
+        warnings.simplefilter("ignore", category=DeprecationWarning)
+        df = vcf.relatedness(gap=0, linkage_max=2)
+        assert len(w) == 1
+        assert "tested:" in str(w[-1].message)
     assert "ibs0" in df, df
     assert "rel" in df
     #vcf = VCF(VCF_PATH, gts012=True)
@@ -202,7 +215,8 @@ def test_phases():
     assert not any(v.gt_phases)
 
 def test_bad_init():
-    assert_raises(Exception, VCF, "XXXXX")
+    with pytest.raises(Exception):
+        VCF("XXXXX")
 
 def test_samples():
     v = VCF(VCF_PATH)
@@ -214,7 +228,8 @@ def test_next():
     assert isinstance(variant, Variant)
 
 def test_variant():
-    assert_raises(TypeError, Variant)
+    with pytest.raises(TypeError):
+        Variant()
 
 def test_info_dict():
     v = VCF(VCF_PATH)
@@ -247,7 +262,8 @@ def test_attrs():
 def test_empty():
     p = os.path.join(HERE, "empty.vcf")
     assert os.path.exists(p)
-    assert_raises(IOError, VCF, p)
+    with pytest.raises(IOError):
+        VCF(p)
 
 def test_format_field():
     vcf = VCF(VCF_PATH)
@@ -269,7 +285,6 @@ def test_writer_from_string():
     w.close()
 
 def test_isa():
-
     vcf = VCF(os.path.join(HERE, "test.isa.vcf"))
     for i, v in enumerate(vcf):
         if i in {0, 1, 2, 3}:
@@ -321,6 +336,36 @@ def test_writer():
     with open(VCF_PATH) as fp:
         run_writer(Writer(fp, v), f, rec)
 
+def test_filters():
+    v = VCF(VCF_PATH)
+    f = tempfile.mktemp(suffix=".vcf")
+    atexit.register(os.unlink, f)
+    rec = next(v)
+
+    writer = Writer(f, v)
+
+    rec.INFO["AC"] = "3"
+    rec.FILTER = ["LowQual"]
+    writer.write_record(rec)
+
+    rec.FILTER = ["LowQual", "VQSRTrancheSNP99.90to100.00"]
+    writer.write_record(rec)
+
+    rec.FILTER = "PASS"
+    writer.write_record(rec)
+
+    rec.FILTER = []
+    writer.write_record(rec)
+
+    writer.close()
+
+    expected_filter = ["LowQual", "LowQual;VQSRTrancheSNP99.90to100.00", None, None]
+    expected_filters = [["LowQual"], ["LowQual", "VQSRTrancheSNP99.90to100.00"], ["PASS"], []]
+
+    for i, variant in enumerate(VCF(f)):
+        assert variant.FILTER == expected_filter[i], (variant.FILTER, expected_filter[i])
+        assert variant.FILTERS == expected_filters[i], (variant.FILTERS, expected_filters[i])
+
 def test_add_info_to_header():
     v = VCF(VCF_PATH)
     v.add_info_to_header({'ID': 'abcdefg', 'Description': 'abcdefg',
@@ -377,7 +422,8 @@ def test_add_flag():
     fh = VCF(f)
     v = next(fh)
     fh.close()
-    assert_raises(KeyError, v.INFO.__getitem__, "myflag")
+    with pytest.raises(KeyError):
+        v.INFO["myflag"]
 
 def test_issue198():
     vcf = VCF(os.path.join(HERE, "issue_198.vcf"), strict_gt=True)
@@ -434,7 +480,7 @@ def test_seqnames():
 
 def test_different_index():
     b = VCF('{}/test.snpeff.bcf'.format(HERE), threads=3)
-    b.set_index("cyvcf2/tests/test-diff.csi")
+    b.set_index("{}/test-diff.csi".format(HERE))
     s = 0
     for r in b("chr1:69427-69429"):
         s += 1
@@ -454,16 +500,17 @@ def test_var_type():
 def _get_line_for(v):
     import gzip
 
-    for i, line in enumerate(gzip.open(VCF_PATH), start=1):
-        line = line.decode()
-        if line[0] == "#": continue
-        toks = line.strip().split("\t")
-        if not (toks[0] == v.CHROM and int(toks[1]) == v.POS): continue
-        if toks[3] != v.REF: continue
-        if toks[4] not in v.ALT: continue
-        return toks
-    else:
-        raise Exception("not found")
+    with gzip.open(VCF_PATH) as f:
+        for i, line in enumerate(f, start=1):
+            line = line.decode()
+            if line[0] == "#": continue
+            toks = line.strip().split("\t")
+            if not (toks[0] == v.CHROM and int(toks[1]) == v.POS): continue
+            if toks[3] != v.REF: continue
+            if toks[4] not in v.ALT: continue
+            return toks
+        else:
+            raise Exception("not found")
 
 
 def _get_samples(v):
@@ -482,7 +529,7 @@ def _get_samples(v):
         return 2
     toks = _get_line_for(v)
     samples = toks[9:]
-    return np.array([_get_gt(s) for s in samples], np.int)
+    return np.array([_get_gt(s) for s in samples], np.int32)
 
 def test_header_info():
     v = VCF(VCF_PATH)
@@ -491,7 +538,8 @@ def test_header_info():
     assert "Description" in csq
 
 
-    assert_raises(KeyError, v.__getitem__, b'XXXXX')
+    with pytest.raises(KeyError):
+        v[b'XXXXX']
 
 def test_snpeff_header():
     v = VCF(VCF_PATH2)
@@ -613,13 +661,24 @@ def test_bcf():
     viter = vcf("1:69260-69438")
     sys.stderr.write("\nOK\n")
     sys.stderr.flush()
-    l = list(viter)
+    with warnings.catch_warnings(record=True) as w:
+        l = list(viter)
+        assert len(w) == 1
+        assert "no intervals found" in str(w[-1].message)
     assert len(l) == 0, len(l)
 
     iter = vcf("chr1:69260-69438")
     l = list(iter)
     assert len(l) == 2, len(l)
 
+def test_vcf_no_intervals():
+    vcf = VCF('{}/test.vcf.gz'.format(HERE))
+    viter = vcf("not_a_chrom")
+    with warnings.catch_warnings(record=True) as w:
+        l = list(viter)
+        assert len(w) == 1
+        assert "no intervals found" in str(w[-1].message)
+    assert len(l) == 0, len(l)
 
 def test_issue12():
     fields = "ADP_ALL ADPD ADPO ADP_PASS ADPR AFR AMBIG BMF_PASS BMF_QUANT AF_FAILED FA_FAILED FM_FAILED FP_FAILED FR_FAILED MD_FAILED IMPROPER MQ_FAILED OVERLAP PV_FAILED QSS".split()
@@ -634,7 +693,8 @@ def test_issue12():
         vals = v.format("RVF")
         assert vals.dtype in (np.float32, np.float64)
 
-    assert_raises(KeyError, v.format, "RULE")
+    with pytest.raises(KeyError):
+        v.format("RULE")
 
 def test_gt_bases_nondiploid():
     """Ensure gt_bases works with more complex base representations.
@@ -668,7 +728,7 @@ def test_set_format_int_a():
     vcf = VCF('{}/test-format-string.vcf'.format(HERE))
     assert vcf.add_format_to_header(dict(ID="PI", Number=1, Type="Integer", Description="Int example")) == 0
     v = next(vcf)
-    v.set_format("PI", np.array([5, 1], dtype=np.int))
+    v.set_format("PI", np.array([5, 1], dtype=int))
     assert allclose(fmap(float, get_gt_str(v, "PI")), [5, 1])
 
 def test_set_format_int_b():
@@ -693,7 +753,7 @@ def test_set_format_int3():
     vcf = VCF('{}/test-format-string.vcf'.format(HERE))
     assert vcf.add_format_to_header(dict(ID="P3", Number=3, Type="Integer", Description="Int example")) == 0
     v = next(vcf)
-    exp = np.array([[1, 11, 111], [2, 22, 222]], dtype=np.int)
+    exp = np.array([[1, 11, 111], [2, 22, 222]], dtype=int)
     v.set_format("P3", exp)
     res = get_gt_str(v, "P3")
     assert res == ["1,11,111", "2,22,222"], (res, str(v))
@@ -723,7 +783,8 @@ def test_set_format_str_bytes_number3():
     v = next(vcf)
 
     contents = np.array([[b'foo', b'barbaz', b'biz'], [b'blub', b'bloop', b'blop']])
-    assert_raises(Exception, v.set_format, "STR", contents)
+    with pytest.raises(Exception):
+        v.set_format("STR", contents)
 
 def test_set_gts():
     vcf = VCF('{}/test-format-string.vcf'.format(HERE))
@@ -983,7 +1044,10 @@ def test_set_chrom_when_contig_not_in_header():
     assert new_chrom not in original_seqnames
     v = next(vcf)
 
-    v.CHROM = new_chrom
+    with warnings.catch_warnings(record=True) as w:
+        v.CHROM = new_chrom
+        assert len(w) == 1
+        assert "added new contig" in str(w[-1].message)
     assert v.CHROM == new_chrom
     expected_seqnames = sorted(original_seqnames + [new_chrom])
     assert vcf.seqnames == expected_seqnames
@@ -1009,7 +1073,7 @@ def test_set_qual():
     variant.QUAL = 30.0
     assert variant.QUAL == 30.0
 
-    with assert_raises(TypeError):
+    with pytest.raises(TypeError):
         variant.QUAL = "30.0"
 
     variant.QUAL = None
@@ -1018,6 +1082,9 @@ def test_set_qual():
 def test_strict_gt_option_flag():
     test_vcf = '{}/test-strict-gt-option-flag.vcf.gz'.format(HERE)
 
+     #T, C
+     #0/0     1/1     0/1     1/0     1/.     ./1     0/.     ./0     ./.
+
     truth_gt_bases = ('T/T', 'C/C', 'T/C', 'C/T', 'C/.', './C', 'T/.', './T', './.')
     truth_genotypes = (
         [0, 0, False],
@@ -1036,7 +1103,11 @@ def test_strict_gt_option_flag():
 
     msg = "VCF(gts012=False, strict_gt=False) not working"
     truth_gt_types = (0, 3, 1, 1, 1, 1, 0, 0, 2)
+    print(variant.gt_bases.tolist(), file=sys.stderr)
+    print(variant.gt_types.tolist(), file=sys.stderr)
     assert bool(tuple(variant.gt_bases.tolist()) == truth_gt_bases), '{} [gt_bases]'.format(msg)
+
+    """
     assert bool(tuple(variant.gt_types.tolist()) == truth_gt_types), '{} [gt_types]'.format(msg)
     assert bool(tuple(variant.genotypes) == truth_genotypes), '{} (genotypes)'.format(msg)
 
@@ -1069,6 +1140,7 @@ def test_strict_gt_option_flag():
     assert tuple(variant.gt_bases.tolist()) == truth_gt_bases, '{} [gt_bases]'.format(msg)
     assert tuple(variant.gt_types.tolist()) == truth_gt_types, '{} [gt_types]'.format(msg)
     assert tuple(variant.genotypes) == truth_genotypes, '{} (genotypes)'.format(msg)
+    """
 
 def test_alt_repr():
     v = os.path.join(HERE, "test-alt-repr.vcf")
@@ -1103,7 +1175,8 @@ def test_closed_iter():
     vcf = VCF(path, gts012=True, strict_gt=False)
     vcf.close()
 
-    assert_raises(Exception, next, vcf)
+    with pytest.raises(Exception):
+        next(vcf)
 
 def test_issue72():
     path = os.path.join(HERE, "test-alt-repr.vcf")
@@ -1165,9 +1238,8 @@ def test_no_seqlen():
     vcf_path = os.path.join(HERE, "no-seq-len.vcf")
     vcf = VCF(vcf_path)
     assert vcf.seqnames == ["3"]
-    with assert_raises(AttributeError) as ae:
+    with pytest.raises(AttributeError):
         vcf.seqlens
-    assert isinstance(ae.exception, AttributeError)
 
 def test_set_unknown_format():
     vcf = VCF(VCF_PATH)
@@ -1186,4 +1258,47 @@ def test_invalid_header():
     # htslib produces the error "Empty sample name: trailing spaces/tabs in the header line?"
     p = os.path.join(HERE, "test-invalid-header.vcf")
     assert os.path.exists(p)
-    assert_raises(Exception, VCF, p)
+    with pytest.raises(Exception):
+        VCF(p)
+
+
+def test_genotypes():
+    """
+. 1
+./. ./1
+./. 1
+0/1 0
+0 0/1
+     """
+    exp_array = [[-1,  0],
+       [-1, -1,  0],
+       [-1, -1,  0],
+       [0, 1,  0],
+       [0, -2, 1],
+       ]
+
+    non_strict_exp_num = [
+    [0, 0, 1, 1],
+    [0, 1, 1, 0],
+    [0, 0, 1, 1],
+    [1, 1, 0, 0],
+    [1, 1, 0, 0],
+    ] 
+
+    strict_exp_num = [x[:] for x in non_strict_exp_num]
+    strict_exp_num[1] = [0, 0, 2, 0] # both unknown
+
+    for strict_gt in (False, True):
+        vcf = VCF(os.path.join(HERE, "test-genotypes.vcf"), strict_gt=strict_gt)
+
+        exp_num = strict_exp_num if strict_gt else non_strict_exp_num
+
+
+        for i, v in enumerate(vcf):
+            #if i != 3: continue
+            obs = [v.num_hom_ref, v.num_het, v.num_unknown, v.num_hom_alt]
+            assert obs == exp_num[i], ("error with num_*")
+
+            a = v.genotype.array()[0] # only 0'th item
+            print("i:", i, " a:", v.genotype.array()[0], " exp:", exp_array[i])
+            assert (a == exp_array[i]).all(), " error with array"


=====================================
docs/source/index.rst
=====================================
@@ -131,11 +131,11 @@ or via bioconda.
 Testing
 =======
 
-Tests can be run with:
+Install `pytest`, then tests can be run with:
 
 .. code-block:: bash
 
-    python setup.py test
+    pytest
 
 Known Limitations
 =================


=====================================
setup.cfg
=====================================
@@ -1,5 +1,2 @@
-[nosetests]
-verbosity=1
-detailed-errors=1
-with-coverage=1
-stop=1
+[tool:pytest]
+testpaths = cyvcf2/tests


=====================================
setup.py
=====================================
@@ -54,9 +54,15 @@ sources += glob.glob('htslib/cram/*.c')
 sources = [x for x in sources if not x.endswith(('htsfile.c', 'tabix.c', 'bgzip.c'))]
 sources.append('cyvcf2/helpers.c')
 
+extra_libs = []
+if platform.system() != 'Darwin':
+    extra_libs.append('crypt')
+if bool(int(os.getenv("LIBDEFLATE", 0))):
+    extra_libs.append('deflate')
+
 extensions = [Extension("cyvcf2.cyvcf2",
                         ["cyvcf2/cyvcf2.pyx"] + sources,
-                        libraries=['z', 'bz2', 'lzma', 'curl', 'ssl'] + (['crypt'] if platform.system() != 'Darwin' else []),
+                        libraries=['z', 'bz2', 'lzma', 'curl', 'ssl'] + extra_libs,
                         extra_compile_args=["-Wno-sign-compare", "-Wno-unused-function",
                             "-Wno-strict-prototypes",
                             "-Wno-unused-result", "-Wno-discarded-qualifiers"],
@@ -96,8 +102,6 @@ setup(
             'cyvcf2 = cyvcf2.__main__:cli',
         ],
     ),
-    test_suite='nose.collector',
-    tests_require='nose',
     install_requires=['numpy', 'coloredlogs', 'click'],
     include_package_data=True,
     zip_safe=False,



View it on GitLab: https://salsa.debian.org/med-team/cyvcf2/-/commit/c6bc65e7f5e664c239c8931d98529699de97b40a

-- 
View it on GitLab: https://salsa.debian.org/med-team/cyvcf2/-/commit/c6bc65e7f5e664c239c8931d98529699de97b40a
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