gm_raw <- trace::example_data
test_fragments <- peak_table_to_fragments(gm_raw,
data_format = "genemapper5",
dye_channel = "B",
min_size_bp = 400
)
find_alleles(
fragments_list = test_fragments,
peak_region_size_gap_threshold = 6,
peak_region_signal_threshold_multiplier = 1
)
extract_alleles(test_fragments)
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