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Fixed cell output table size
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07_querying_lakehouse.ipynb

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@@ -27,7 +27,7 @@
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},
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{
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"cell_type": "code",
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"execution_count": null,
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"execution_count": 3,
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"metadata": {},
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"outputs": [],
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"source": [
@@ -386,30 +386,30 @@
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"name": "stdout",
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"output_type": "stream",
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"text": [
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"+--------------------+---------+------+---------+-------+-------------+---------+--------+-----+------------------+-----+----------------------------+\n",
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"| SequenceRunName|SubjectID|Gender|Phenotype|StudyID| DiseaseCode| SNOMED|SampleID|CHROM| REF| ALT|array_size(alternateAlleles)|\n",
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"+--------------------+---------+------+---------+-------+-------------+---------+--------+-----+------------------+-----+----------------------------+\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| AT| [A]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| C| [T]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| A| [G]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| G| [A]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| G| [A]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| T| [C]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| T| [G]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| G| [A]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| C| [G]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| C| [T]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| T| [G]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| T| [C]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| T| [A]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| G| [A]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| G| [C]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| C| [T]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| A| [G]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| G| [A]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| G|[GAA]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9|AATGTGGGGCATACACAT| [A]| 1|\n",
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"+--------------------+---------+------+---------+-------+-------------+---------+--------+-----+------------------+-----+----------------------------+\n",
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"+--------------------+---------+------+---------+-------+-------------+---------+--------+-----+------------------+-----+-------+\n",
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"| SequenceRunName|SubjectID|Gender|Phenotype|StudyID| DiseaseCode| SNOMED|SampleID|CHROM| REF| ALT|ALT_cnt|\n",
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"+--------------------+---------+------+---------+-------+-------------+---------+--------+-----+------------------+-----+-------+\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| AT| [A]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| C| [T]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| A| [G]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| G| [A]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| G| [A]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| T| [C]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| T| [G]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| G| [A]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| C| [G]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| C| [T]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| T| [G]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| T| [C]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| T| [A]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| G| [A]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| G| [C]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| C| [T]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| A| [G]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| G| [A]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9| G|[GAA]| 1|\n",
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"|221007_A00130_000...| SBJ00001|Female| normal|NA12878|MONDO:0007254|429740004| NA12878| chr9|AATGTGGGGCATACACAT| [A]| 1|\n",
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"+--------------------+---------+------+---------+-------+-------------+---------+--------+-----+------------------+-----+-------+\n",
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"only showing top 20 rows\n",
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"\n"
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]
@@ -418,7 +418,7 @@
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"source": [
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"spark.sql(\"select \\\n",
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" m.SequenceRunName, m.SubjectID, m.Gender, m.Phenotype, m.StudyID, m.DiseaseCode, m.SNOMED, m.SampleID, \\\n",
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" s.contigName as CHROM, s.referenceAllele as REF, s.alternateAlleles as ALT, array_size(s.alternateAlleles) \\\n",
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" s.contigName as CHROM, s.referenceAllele as REF, s.alternateAlleles as ALT, array_size(s.alternateAlleles) as ALT_cnt \\\n",
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"from metadata_table as m \\\n",
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"join somatic_table as s on s.genotypes_sampleId = m.SampleID\").show()"
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]

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