diff --git a/haptools/data/genotypes.py b/haptools/data/genotypes.py
index 4d812d10..f6179f13 100644
--- a/haptools/data/genotypes.py
+++ b/haptools/data/genotypes.py
@@ -1543,14 +1543,39 @@ def _num_unique_alleles(self, arr: npt.NDArray):
         allele_cts[allele_cts < 2] = 2
         return allele_cts
 
-    def write(self):
+    def write(self, dosages: npt.NDArray = None):
         """
         Write the variants in this class to PLINK2 files at
         :py:attr:`~.GenotypesPLINK.fname`
+
+        Parameters
+        ----------
+        dosages : npt.NDArray[np.float32|np.float64]
+            A matrix of dosages of shape (num_variants, num_samples) and float dtype
         """
         # write the psam and pvar files
         self.write_samples()
         self.write_variants()
+        if dosages is not None:
+            self.log.info("Writing dosages instead of genotypes")
+            if (dosages.shape[0] != self.data.shape[1]) and (
+                dosages.shape[1] != self.data.shape[0]
+            ):
+                raise ValueError(
+                    "Dosage array must be of shape num_variants x num_samples"
+                )
+            pv = pgenlib.PvarReader(bytes(str(self.fname.with_suffix(".pvar")), "utf8"))
+            with pgenlib.PgenWriter(
+                filename=bytes(str(self.fname), "utf8"),
+                sample_ct=len(self.samples),
+                variant_ct=len(self.variants),
+                allele_ct_limit=pv.get_max_allele_ct(),
+                nonref_flags=False,
+                hardcall_phase_present=True,
+                dosage_present=True,
+            ) as pgen:
+                pgen.append_dosages_batch(dosages)
+            return
         self.log.debug(f"Transposing genotype matrix of size {self.data.shape}")
         # transpose the data b/c pgenwriter expects things in "variant-major" order
         # (ie where variants are rows instead of samples)
@@ -1822,7 +1847,7 @@ def _iterate(
             variant.data[:, :2][missing] = np.iinfo(np.uint8).max
             yield variant
 
-    def write(self):
+    def write(self, dosages: npt.NDArray = None):
         raise NotImplementedError
 
     def write_variants(self):
diff --git a/tests/test_data.py b/tests/test_data.py
index 36377ce3..ec1e39b2 100644
--- a/tests/test_data.py
+++ b/tests/test_data.py
@@ -658,6 +658,35 @@ def test_write_genotypes_biallelic(self):
         fname.with_suffix(".pvar").unlink()
         fname.unlink()
 
+    def test_write_genotypes_biallelic_dosage(self):
+        gts = self._get_fake_genotypes_plink()
+
+        # convert to bool - we should be able to handle both
+        gts.data = gts.data.astype(np.bool_)
+
+        fname = DATADIR / "test_write.pgen"
+        gts.fname = fname
+        fake_dosages = gts.data[:, :, :2].sum(axis=2)
+        gts.write(dosages=fake_dosages.T.copy().astype(np.float32))
+
+        new_gts = GenotypesPLINK(fname)
+        new_gts.read()
+
+        # check that everything matches what we expected
+        np.testing.assert_allclose(
+            gts.data[:, :, :2].sum(axis=2),
+            new_gts.data[:, :, :2].sum(axis=2),
+        )
+        assert gts.samples == new_gts.samples
+        for i in range(len(new_gts.variants)):
+            for col in ("chrom", "pos", "id", "alleles"):
+                assert gts.variants[col][i] == new_gts.variants[col][i]
+
+        # clean up afterwards: delete the files we created
+        fname.with_suffix(".psam").unlink()
+        fname.with_suffix(".pvar").unlink()
+        fname.unlink()
+
     def test_write_multiallelic(self):
         # Create fake multi-allelic genotype data to write to the PLINK file
         gts_multiallelic = self._get_fake_genotypes_multiallelic()