Commit
·
d4aacab
1
Parent(s):
819d018
fix
Browse files
.gitattributes
CHANGED
@@ -53,6 +53,5 @@ saved_model/**/* filter=lfs diff=lfs merge=lfs -text
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*.jpg filter=lfs diff=lfs merge=lfs -text
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*.jpeg filter=lfs diff=lfs merge=lfs -text
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*.webp filter=lfs diff=lfs merge=lfs -text
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transcript_expression/
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transcript_expression/
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transcript_expression/transcript_coordinates.csv filter=lfs diff=lfs merge=lfs -text
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*.jpg filter=lfs diff=lfs merge=lfs -text
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*.jpeg filter=lfs diff=lfs merge=lfs -text
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*.webp filter=lfs diff=lfs merge=lfs -text
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transcript_expression/GTEx_df_v1.csv filter=lfs diff=lfs merge=lfs -text
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transcript_expression/GTEx_df_v2.csv filter=lfs diff=lfs merge=lfs -text
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multi_omics_transcript_expression.py
CHANGED
@@ -32,6 +32,96 @@ Task Specific Handlers:
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logger = logging.getLogger("multi_omics_transcript_expression")
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logger.setLevel("INFO")
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class GenomicLRATaskHandler(ABC):
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"""
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@@ -195,12 +285,8 @@ class TranscriptExpressionHandler(GenomicLRATaskHandler):
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)
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self.reference_genome = Fasta(reference_genome_file, one_based_attributes=False)
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self.
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"transcript_expression/
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)
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self.labels_csv_file = dl_manager.download_and_extract(
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"transcript_expression/expression_values_v2.csv"
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)
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return super().split_generators(dl_manager, cache_dir_root)
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@@ -211,18 +297,17 @@ class TranscriptExpressionHandler(GenomicLRATaskHandler):
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and the corresponding labels. The sequences are padded to the correct sequence
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length and standardized before returning.
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"""
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labels_name = labels_df.columns[2:]
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key = 0
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for idx, coordinates_row in
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start = coordinates_row["position"] - 1 # -1 since vcf coords are 1-based
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chromosome = coordinates_row["chr"]
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labels_row =
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padded_sequence = pad_sequence(
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chromosome=self.reference_genome[chromosome],
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start=start,
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@@ -241,7 +326,7 @@ class TranscriptExpressionHandler(GenomicLRATaskHandler):
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}
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key += 1
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logger.info(
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f"filtering out {len(
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f"elements from the dataset"
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)
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logger = logging.getLogger("multi_omics_transcript_expression")
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logger.setLevel("INFO")
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LABELS_V1 = [
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"Adipose Tissue",
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"Adrenal Gland",
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"Bladder",
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"Blood",
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"Blood Vessel",
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"Brain",
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"Breast",
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"Cervix Uteri",
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"Colon",
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"Esophagus",
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"Fallopian Tube",
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"Heart",
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"Kidney",
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"Liver",
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"Lung",
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"Muscle",
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"Nerve",
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"Ovary",
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"Pancreas",
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"Pituitary",
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"Prostate",
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"Salivary Gland",
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"Skin",
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"Small Intestine",
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"Spleen",
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"Stomach",
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"Testis",
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"Thyroid",
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"Uterus",
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"Vagina",
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]
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LABELS_V2 = [
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"Adipose_Subcutaneous",
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"Adipose_Visceral (Omentum)",
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"Adrenal Gland",
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"Artery_Aorta",
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"Artery_Coronary",
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"Artery_Tibial",
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"Bladder",
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"Brain_Amygdala",
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"Brain_Anterior cingulate cortex (BA24)",
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"Brain_Caudate (basal ganglia)",
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"Brain_Cerebellar Hemisphere",
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"Brain_Cerebellum",
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"Brain_Cortex",
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"Brain_Frontal Cortex (BA9)",
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"Brain_Hippocampus",
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"Brain_Hypothalamus",
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"Brain_Nucleus accumbens (basal ganglia)",
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"Brain_Putamen (basal ganglia)",
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"Brain_Spinal cord (cervical c-1)",
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"Brain_Substantia nigra",
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"Breast_Mammary Tissue",
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"Cells_Cultured fibroblasts",
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"Cells_EBV-transformed lymphocytes",
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"Cervix_Ectocervix",
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"Cervix_Endocervix",
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"Colon_Sigmoid",
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"Colon_Transverse",
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"Esophagus_Gastroesophageal Junction",
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"Esophagus_Mucosa",
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"Esophagus_Muscularis",
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"Fallopian Tube",
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"Heart_Atrial Appendage",
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"Heart_Left Ventricle",
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"Kidney_Cortex",
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"Kidney_Medulla",
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"Liver",
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"Lung",
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"Minor Salivary Gland",
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"Muscle_Skeletal",
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"Nerve_Tibial",
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"Ovary",
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"Pancreas",
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"Pituitary",
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"Prostate",
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"Skin_Not Sun Exposed (Suprapubic)",
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"Skin_Sun Exposed (Lower leg)",
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"Small Intestine_Terminal Ileum",
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"Spleen",
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"Stomach",
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"Testis",
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"Thyroid",
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"Uterus",
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"Vagina",
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"Whole Blood",
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]
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class GenomicLRATaskHandler(ABC):
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"""
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)
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self.reference_genome = Fasta(reference_genome_file, one_based_attributes=False)
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self.df_csv_file = dl_manager.download_and_extract(
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"transcript_expression/GTEx_df_v1.csv"
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)
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return super().split_generators(dl_manager, cache_dir_root)
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and the corresponding labels. The sequences are padded to the correct sequence
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length and standardized before returning.
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"""
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df = pd.read_csv(self.df_csv_file)
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labels_name = LABELS_V1
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split_df = df.loc[df["split"] == split]
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key = 0
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for idx, coordinates_row in split_df.iterrows():
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start = coordinates_row["position"] - 1 # -1 since vcf coords are 1-based
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chromosome = coordinates_row["chr"]
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labels_row = coordinates_row.iloc[LABELS_V1]
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padded_sequence = pad_sequence(
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chromosome=self.reference_genome[chromosome],
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start=start,
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}
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key += 1
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logger.info(
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f"filtering out {len(split_df)-key} "
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f"elements from the dataset"
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)
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transcript_expression/transcript_coordinates.csv
DELETED
@@ -1,3 +0,0 @@
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version https://git-lfs.github.com/spec/v1
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oid sha256:6a5ee8afeb870a22e4bc6cef3de694c4107571972f10efe52788122bb87b6820
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size 5237763
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