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23 | 23 | # tests/data/vcf/sample-variants.vcf.gz |
24 | 24 |
|
25 | 25 |
|
| 26 | +import numpy as np |
26 | 27 | import pytest |
| 28 | +import zarr |
27 | 29 |
|
28 | 30 | from vczstore.append import append |
29 | 31 |
|
@@ -101,6 +103,252 @@ def test_append_fail_alleles_mismatch(tmp_path): |
101 | 103 | append(vcz1, vcz2) |
102 | 104 |
|
103 | 105 |
|
| 106 | +def test_append_fails_for_misaligned_variant_chunks(): |
| 107 | + store1 = zarr.storage.MemoryStore() |
| 108 | + root1 = zarr.create_group(store=store1) |
| 109 | + root1.create_array( |
| 110 | + "contig_id", |
| 111 | + data=np.array(["0"]), |
| 112 | + dimension_names=["contigs"], |
| 113 | + compressors=None, |
| 114 | + filters=None, |
| 115 | + ) |
| 116 | + root1.create_array( |
| 117 | + "variant_contig", |
| 118 | + data=np.array([0, 0], dtype=np.int32), |
| 119 | + chunks=(2,), |
| 120 | + dimension_names=["variants"], |
| 121 | + compressors=None, |
| 122 | + filters=None, |
| 123 | + ) |
| 124 | + root1.create_array( |
| 125 | + "variant_position", |
| 126 | + data=np.array([1, 2], dtype=np.int32), |
| 127 | + chunks=(2,), |
| 128 | + dimension_names=["variants"], |
| 129 | + compressors=None, |
| 130 | + filters=None, |
| 131 | + ) |
| 132 | + root1.create_array( |
| 133 | + "variant_allele", |
| 134 | + data=np.array([["A", "T"], ["C", "G"]]), |
| 135 | + chunks=(2, 2), |
| 136 | + dimension_names=["variants", "alleles"], |
| 137 | + compressors=None, |
| 138 | + filters=None, |
| 139 | + ) |
| 140 | + root1.create_array( |
| 141 | + "sample_id", |
| 142 | + data=np.array(["S1"]), |
| 143 | + dimension_names=["samples"], |
| 144 | + compressors=None, |
| 145 | + filters=None, |
| 146 | + ) |
| 147 | + root1.create_array( |
| 148 | + "call_genotype", |
| 149 | + data=np.array([[[0, 1]], [[1, 1]]], dtype=np.int8), |
| 150 | + chunks=(1, 1, 2), |
| 151 | + dimension_names=["variants", "samples", "ploidy"], |
| 152 | + compressors=None, |
| 153 | + filters=None, |
| 154 | + ) |
| 155 | + |
| 156 | + store2 = zarr.storage.MemoryStore() |
| 157 | + root2 = zarr.create_group(store=store2) |
| 158 | + for name in ("contig_id", "variant_contig", "variant_position", "variant_allele"): |
| 159 | + root2.create_array( |
| 160 | + name, |
| 161 | + data=root1[name][:], |
| 162 | + chunks=root1[name].chunks, |
| 163 | + dimension_names=root1[name].metadata.dimension_names, |
| 164 | + compressors=None, |
| 165 | + filters=None, |
| 166 | + ) |
| 167 | + root2.create_array( |
| 168 | + "sample_id", |
| 169 | + data=np.array(["S2"]), |
| 170 | + dimension_names=["samples"], |
| 171 | + compressors=None, |
| 172 | + filters=None, |
| 173 | + ) |
| 174 | + root2.create_array( |
| 175 | + "call_genotype", |
| 176 | + data=np.array([[[0, 0]], [[0, 1]]], dtype=np.int8), |
| 177 | + chunks=(2, 1, 2), |
| 178 | + dimension_names=["variants", "samples", "ploidy"], |
| 179 | + compressors=None, |
| 180 | + filters=None, |
| 181 | + ) |
| 182 | + |
| 183 | + with pytest.raises(ValueError, match="VCZ-aligned variant chunks"): |
| 184 | + append(store1, store2) |
| 185 | + |
| 186 | + root1_after = zarr.open_group(store=store1, mode="r") |
| 187 | + np.testing.assert_array_equal(root1_after["sample_id"][:], np.array(["S1"])) |
| 188 | + |
| 189 | + |
| 190 | +def test_append_fails_before_mutating_when_source_call_array_is_missing(): |
| 191 | + store1 = zarr.storage.MemoryStore() |
| 192 | + root1 = zarr.create_group(store=store1) |
| 193 | + root1.create_array( |
| 194 | + "contig_id", |
| 195 | + data=np.array(["0"]), |
| 196 | + dimension_names=["contigs"], |
| 197 | + compressors=None, |
| 198 | + filters=None, |
| 199 | + ) |
| 200 | + root1.create_array( |
| 201 | + "variant_contig", |
| 202 | + data=np.array([0, 0], dtype=np.int32), |
| 203 | + chunks=(2,), |
| 204 | + dimension_names=["variants"], |
| 205 | + compressors=None, |
| 206 | + filters=None, |
| 207 | + ) |
| 208 | + root1.create_array( |
| 209 | + "variant_position", |
| 210 | + data=np.array([1, 2], dtype=np.int32), |
| 211 | + chunks=(2,), |
| 212 | + dimension_names=["variants"], |
| 213 | + compressors=None, |
| 214 | + filters=None, |
| 215 | + ) |
| 216 | + root1.create_array( |
| 217 | + "variant_allele", |
| 218 | + data=np.array([["A", "T"], ["C", "G"]]), |
| 219 | + chunks=(2, 2), |
| 220 | + dimension_names=["variants", "alleles"], |
| 221 | + compressors=None, |
| 222 | + filters=None, |
| 223 | + ) |
| 224 | + root1.create_array( |
| 225 | + "sample_id", |
| 226 | + data=np.array(["S1"]), |
| 227 | + dimension_names=["samples"], |
| 228 | + compressors=None, |
| 229 | + filters=None, |
| 230 | + ) |
| 231 | + root1.create_array( |
| 232 | + "call_genotype", |
| 233 | + data=np.array([[[0, 1]], [[1, 1]]], dtype=np.int8), |
| 234 | + chunks=(2, 1, 2), |
| 235 | + dimension_names=["variants", "samples", "ploidy"], |
| 236 | + compressors=None, |
| 237 | + filters=None, |
| 238 | + ) |
| 239 | + |
| 240 | + store2 = zarr.storage.MemoryStore() |
| 241 | + root2 = zarr.create_group(store=store2) |
| 242 | + for name in ("contig_id", "variant_contig", "variant_position", "variant_allele"): |
| 243 | + root2.create_array( |
| 244 | + name, |
| 245 | + data=root1[name][:], |
| 246 | + chunks=root1[name].chunks, |
| 247 | + dimension_names=root1[name].metadata.dimension_names, |
| 248 | + compressors=None, |
| 249 | + filters=None, |
| 250 | + ) |
| 251 | + root2.create_array( |
| 252 | + "sample_id", |
| 253 | + data=np.array(["S2"]), |
| 254 | + dimension_names=["samples"], |
| 255 | + compressors=None, |
| 256 | + filters=None, |
| 257 | + ) |
| 258 | + |
| 259 | + with pytest.raises(ValueError, match="present in both stores"): |
| 260 | + append(store1, store2) |
| 261 | + |
| 262 | + root1_after = zarr.open_group(store=store1, mode="r") |
| 263 | + np.testing.assert_array_equal(root1_after["sample_id"][:], np.array(["S1"])) |
| 264 | + assert root1_after["call_genotype"].shape == (2, 1, 2) |
| 265 | + |
| 266 | + |
| 267 | +def test_append_fails_for_misaligned_source_variant_chunks(): |
| 268 | + store1 = zarr.storage.MemoryStore() |
| 269 | + root1 = zarr.create_group(store=store1) |
| 270 | + root1.create_array( |
| 271 | + "contig_id", |
| 272 | + data=np.array(["0"]), |
| 273 | + dimension_names=["contigs"], |
| 274 | + compressors=None, |
| 275 | + filters=None, |
| 276 | + ) |
| 277 | + root1.create_array( |
| 278 | + "variant_contig", |
| 279 | + data=np.array([0, 0], dtype=np.int32), |
| 280 | + chunks=(2,), |
| 281 | + dimension_names=["variants"], |
| 282 | + compressors=None, |
| 283 | + filters=None, |
| 284 | + ) |
| 285 | + root1.create_array( |
| 286 | + "variant_position", |
| 287 | + data=np.array([1, 2], dtype=np.int32), |
| 288 | + chunks=(2,), |
| 289 | + dimension_names=["variants"], |
| 290 | + compressors=None, |
| 291 | + filters=None, |
| 292 | + ) |
| 293 | + root1.create_array( |
| 294 | + "variant_allele", |
| 295 | + data=np.array([["A", "T"], ["C", "G"]]), |
| 296 | + chunks=(2, 2), |
| 297 | + dimension_names=["variants", "alleles"], |
| 298 | + compressors=None, |
| 299 | + filters=None, |
| 300 | + ) |
| 301 | + root1.create_array( |
| 302 | + "sample_id", |
| 303 | + data=np.array(["S1"]), |
| 304 | + dimension_names=["samples"], |
| 305 | + compressors=None, |
| 306 | + filters=None, |
| 307 | + ) |
| 308 | + root1.create_array( |
| 309 | + "call_genotype", |
| 310 | + data=np.array([[[0, 1]], [[1, 1]]], dtype=np.int8), |
| 311 | + chunks=(2, 1, 2), |
| 312 | + dimension_names=["variants", "samples", "ploidy"], |
| 313 | + compressors=None, |
| 314 | + filters=None, |
| 315 | + ) |
| 316 | + |
| 317 | + store2 = zarr.storage.MemoryStore() |
| 318 | + root2 = zarr.create_group(store=store2) |
| 319 | + for name in ("contig_id", "variant_contig", "variant_position", "variant_allele"): |
| 320 | + root2.create_array( |
| 321 | + name, |
| 322 | + data=root1[name][:], |
| 323 | + chunks=root1[name].chunks, |
| 324 | + dimension_names=root1[name].metadata.dimension_names, |
| 325 | + compressors=None, |
| 326 | + filters=None, |
| 327 | + ) |
| 328 | + root2.create_array( |
| 329 | + "sample_id", |
| 330 | + data=np.array(["S2"]), |
| 331 | + dimension_names=["samples"], |
| 332 | + compressors=None, |
| 333 | + filters=None, |
| 334 | + ) |
| 335 | + root2.create_array( |
| 336 | + "call_genotype", |
| 337 | + data=np.array([[[0, 0]], [[0, 1]]], dtype=np.int8), |
| 338 | + chunks=(1, 1, 2), |
| 339 | + dimension_names=["variants", "samples", "ploidy"], |
| 340 | + compressors=None, |
| 341 | + filters=None, |
| 342 | + ) |
| 343 | + |
| 344 | + with pytest.raises(ValueError, match="VCZ-aligned variant chunks"): |
| 345 | + append(store1, store2) |
| 346 | + |
| 347 | + root1_after = zarr.open_group(store=store1, mode="r") |
| 348 | + np.testing.assert_array_equal(root1_after["sample_id"][:], np.array(["S1"])) |
| 349 | + assert root1_after["call_genotype"].shape == (2, 1, 2) |
| 350 | + |
| 351 | + |
104 | 352 | def test_append_multiple_chunks(tmp_path): |
105 | 353 | vcz1 = convert_vcf_to_vcz( |
106 | 354 | "chr22-part1.vcf.gz", tmp_path, variants_chunk_size=10, samples_chunk_size=50 |
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