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24 changes: 14 additions & 10 deletions README.md
Original file line number Diff line number Diff line change
Expand Up @@ -10,36 +10,40 @@ Parsing tools for GTF (gene transfer format) files.

# Example usage

## Parsing all rows of a GTF file into a Pandas DataFrame
## Parsing all rows of a GTF file into a DataFrame

`read_gtf` returns a Polars DataFrame. Pass `result_type="pandas"` to get a
pandas DataFrame instead.

```python
import polars
from gtfparse import read_gtf

# returns GTF with essential columns such as "feature", "seqname", "start", "end"
# alongside the names of any optional keys which appeared in the attribute column
df = read_gtf("gene_annotations.gtf")

# filter DataFrame to gene entries on chrY
df_genes = df[df["feature"] == "gene"]
df_genes_chrY = df_genes[df_genes["seqname"] == "Y"]
df_genes = df.filter(polars.col("feature") == "gene")
df_genes_chrY = df_genes.filter(polars.col("seqname") == "Y")

# all rows (gene, transcripts, exons, ...) for one gene
df_tp53 = df.filter(polars.col("gene_id") == "ENSG00000141510")
```


## Getting gene FPKM values from a StringTie GTF file
## Getting transcript FPKM values from a StringTie GTF file

```python
import polars
from gtfparse import read_gtf

df = read_gtf(
"Transcripts.gtf",
column_converters={"FPKM": float})

gene_fpkms = {
gene_name: fpkm
for (gene_name, fpkm, feature)
in zip(df["seqname"], df["FPKM"], df["feature"])
if feature == "gene"
}
transcripts = df.filter(polars.col("feature") == "transcript")
transcript_fpkms = dict(zip(transcripts["transcript_id"], transcripts["FPKM"]))
```


2 changes: 1 addition & 1 deletion gtfparse/__init__.py
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Expand Up @@ -24,7 +24,7 @@
)
from .write_gtf import write_gtf

__version__ = "2.8.0"
__version__ = "2.8.1"

__all__ = [
"GENCODE_BIOTYPE_ALIASES",
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