View source: R/sequence_position_handling.R
extract_mismatch_positions | R Documentation |
This function filters a dataframe for reads that contain mismatches when compared to the reference genome, as indicated by the MD tag within the BAM data. It then extracts the genomic positions of these mismatches, providing a detailed account of where the sequencing reads do not match the reference sequence.
extract_mismatch_positions(bam_df)
bam_df |
A dataframe obtained from the |
A dataframe of mismatch positions, which includes the genomic positions of all identified mismatches across the reads.
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